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Young people’s perspectives of foster placement instability: A grounded theory approach Ruth Hunter Submitted for the Degree of Doctor of Psychology (Clinical Psychology) School of Psychology Faculty of Arts and Human Sciences University of Surrey Guildford, Surrey 1
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Young people’s perspectives of foster placement instability: A grounded theory

approach

Ruth Hunter

Submitted for the Degree of

Doctor of Psychology(Clinical Psychology)

School of PsychologyFaculty of Arts and Human Sciences

University of SurreyGuildford, SurreyUnited Kingdom

July 2015

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Abstract

This qualitative grounded theory study aimed to explore experiences of

placement moves for young people in foster care, an area neglected in

previous studies. For young people these moves were distressing

experiences of loss and uncertainty that they frequently lacked support to

manage. Consequently the young people felt the need to be self-sufficient

for their emotional needs. However this self-sufficiency often increased

instability and distress as they struggled to influence others or withdrew in

self-protection. Despite this, the young people displayed resilience and

were hopeful for a better life after care.

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Acknowledgements

To all those who have played a role in my path up to this point, thank you.

This achievement is partly yours. Unsurprisingly this encompasses a large

number of people in my personal and professional life. But I would

particularly like to thank God, my parents, my family and those closest to

me. Thank you sounds so simple but I hope you realise just how grateful I

am.

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Contents

MRP Empirical Paper 5

MRP Empirical Paper Appendices 64

MRP Proposal 104

MRP Literature Review 124

Brief Overview of Clinical Experience 192

Table of all Academic Assessments 195

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MRP Empirical Paper

Young people’s perspectives of foster placement instability: A grounded theory approach

ByRuth Joanne Hunter

Submitted in partial fulfilment of the degree of Doctor of Psychology (Clinical Psychology)

School of Psychology Faculty of Arts and Human Sciences

University of SurreyMay 2015

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Abstract

This qualitative grounded theory study aimed to explore experiences of

placement moves for young people in foster care, an area neglected in

previous studies. For young people these moves were distressing

experiences of loss and uncertainty that they frequently lacked support to

manage. Consequently the young people felt the need to be self-sufficient

for their emotional needs. However this self-sufficiency often increased

instability and distress as they struggled to influence others or withdrew in

self-protection. Despite this, the young people displayed resilience and

were hopeful for a better life after care.

Introduction

Globally, young people in care are one of the most at-risk groups for a

range of negative outcomes both in childhood and later life (Minty, 1999;

Barber & Delfabbro, 2003; Tapsfield & Collier, 2005; Ford, Vostanis,

Meltzer & Goodman, 2007) as a consequence of early-life experiences

(Newton, Litrownik, & Landsverk, 2000; Rubin, O’Reilly, Luan, & Localio,

2007).

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Placement instability, including unplanned changes, is a major predictor of

negative outcomes from care (Rostill-Brookes, Larkin, Toms, & Churchman,

2011). The literature refers to such changes using terms such as

‘breakdowns’, ‘moves’ and ‘disruptions’ (Unrau, 2007). Research indicates

that multiple placements are associated with an increased risk of

emotional, behavioural and mental health problems and also future

placement breakdowns (Rubin, Alessandrini, Feudtner, Mandell, Localio, &

Hadley, 2007; Strijker, Knorth, & Knot-Dickscheit, 2008; Stott, 2011). An

understanding of what influences placement stability is key in developing

effective interventions to address this and minimise negative outcomes.

Understanding of Placement Stability

The views of all stakeholders need to be included in a comprehensive

understanding of placement breakdowns and efforts to reduce these

(Wilson, Sinclair & Gibbs, 2000). There is an acknowledged lack of

sufficient perspectives of young people, foster carers and social workers,

as well as birth families and other professionals (Rostill-Brookes et al.,

2011; Khoo & Skoog, 2013). The majority of research into placement

instability has used quantitative methods (Unrau, 2007; Rock, Michelson,

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Thomson & Day, 2013), highlighting risk factors such as child problem

behaviours, longer time in care; older age of child; multiple social workers;

and separation from siblings (Koh, Rollock, Cross & Emblen-Manning,

2014; Rock et al., 2013). These quantitative approaches have frequently

relied on psychometric or standardised measures, often failing to reliably

represent the viewpoints of children or professionals (Unrau, 2007) and

the broader systemic inter-relationships and interactions that may impact

stability. Consequently the complexity of the psychological wellbeing of

the young person has also been overlooked.

Perspectives of those involved in foster care

When perspectives of key stakeholders have been considered, the use of

labels for behaviour such as 'difficult' or 'problematic' highlights a

dominant adult perspective. This perspective has likely been influenced by

the need to retain foster carers through understanding and supporting

them (Sellick, 2006). This focus is reinforced by research showing that the

distress and sense of failure from placement breakdowns reported by

foster carers can lead to reluctance to offer future placements (Nutt,

2006). Unfortunately, this focus on foster carers has resulted in a lack of

appreciation of the child's voice and child and foster carers' interpersonal

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dynamics.

Some attempts to obtain the perspectives of young people have occurred,

but the success of these has been limited by the approaches used. Some

researchers have attempted an indirect approach through seeking foster

carers’ and social workers’ perspectives on the young people’s feelings

and experiences (Unrau, 2007). Sommer, Pramling and Hundeide (2010)

highlighted that gaining valid insight into the experiences of young people

relies on going beyond a 'child perspective' to also include a 'child's

perspective'. A ‘child perspective’ is the adult’s perception on children’s

actions and experiences and perceptions. In contrast a ‘child’s

perspective’ relates to the child’s view on their actions, experiences and

perceptions based on what they view as important.

Obtaining ‘a child’s perspective’

Despite acknowledged difficulties in obtaining young people's

perspectives on care and more specifically placement stability (Gilbertson

& Barber, 2002), an increasing number of studies have attempted to

address this gap of knowledge from the 'child's perspective'. However,

these have often focussed on young people's perspectives of what leads

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to placement breakdowns and the impact of the breakdown, neglecting

the process. For example, Hyde and Kammerer (2009) found that

adolescents in care reported mis-matches between themselves and foster

carers, leading to placement breakdowns. An earlier study by Butler and

Charles (1999) found young people reported difficulties forming

relationships with new carers following placement changes. This gap in

understanding the process has begun to be acknowledged and explored;

Unrau, Seita and Putney (2008) found that foster alumni remembered

breakdowns as significant losses that continued to impact upon

relationship success. However, this study included alumni who had left

care up to 5 decades previously, whose experiences likely differ from

those going through care services today. It is also likely that their

perceptions will have changed over time. Another study into the process

of moves highlighted that young people (9-15 years) wished for the

placement process to be more inclusive and transparent in order to help

them prepare for transitions, both emotionally and practically (Rostill-

Brookes et al., 2011).

Despite this progress, these studies remain at the individual descriptive

level, failing to develop a theoretical understanding of the process and

impact of placement moves for young people. Research needs to go

beyond simply obtaining the ‘child’s perspective’ to responding

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meaningfully to this: Building a coherent understanding of the experiences

and perspectives of young people, grounded in theory to inform a more

comprehensive understanding of placement instability. This can then

inform more effective evidence-based practises to reduce the negative

impact of placement instability and improve the well-being of fostered

young people. This study therefore set out to address this gap and

ascertain what are young people’s perspectives of the process and impact

of foster placement moves?

Approach

Glaser and Strauss’s (1967) Grounded Theory approach was adopted due

to the suitability of this approach for the broad research question as

Grounded Theory is designed to explore phenomena of which little is

known. Furthermore, the inductive approach of Grounded Theory

facilitates the 'discovery' of processes that unfold and give meaning to

social interaction, going beyond merely descriptive accounts of

phenomena (Charmaz, 2006).

Stance of the researcher

Given the approach adopted, an avoidance of a priori assumptions was

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supported through a non-theoretical stance adopted at the outset of the

research. The gap in the area of research was identified but an exploration

of potential applicable theories through a detailed exploration of the

literature was avoided. The aim was to avoid the development of

assumptions and preconceived theories that could increase bias in the

exploration of the data and evolution of the consequent theory.

Consequently, the research question was broad. 1

Aim

This study aimed to explore the process and impact of placement moves

from the perspective of young people in foster care to develop a

preliminary foundation of understanding regarding the psychological

processes and behaviour related to these perspectives. This work will also

aim to provide an early platform for other researchers to further develop a

coherent and theoretically-based account of these phenomena.

Method1 The researcher’s stance and consequent impact on the process are discussed within the method

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The limited knowledge around young people’s perspectives of placement

moves determined a qualitative methodology for the research. It was

considered that young people would recount their experiences in relation

to the social meaning they had attributed to the events, influenced by

their social context. This social constructionist ontological position adopts

a perspective that reality is influenced by social narratives rather than

being fixed, with one 'truth'. This approach enables consideration of how

different perspectives may be located in wider frameworks such as social,

familial, cultural and political contexts. Greig, Taylor and MacKay (2007)

described this as particularly valuable for research involving children, to

enable ethical and useful research that is completed 'with' young people

rather than being 'about' them. Historically, the voices of young people in

foster care have been overlooked or moderated by adults and legal

frameworks. Therefore the value of an approach that enables young

people's voices to retain their own narratives in research is clear.

Data Analysis: Abbreviated Grounded Theory

Grounded Theory does not only aim to collect these experiences but to

develop a framework of understanding. Indeed Glaser and Strauss (1967)

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designed the methodology to enable new theories to 'emerge' whilst

retaining grounding in the context of the data. Further development to this

approach has acknowledged the impact of the researcher’s role in the

process (Willig, 2008) resulting in Charmaz's (2006) Social Constructionist

version of Grounded Theory. This version acknowledges that the actions

and influence of the researcher led to an interpretation of reality rather

than a positivist 'true theory'. Furthermore, this study aimed to take an

inductive approach. It was acknowledged that prior to this study, an

appreciation of the wider topic area was gained from scoping the

research. It was understood that such exploration of the literature could

influence the researcher's analysis of the data, alongside the researcher's

previous experience and values. Reflections were used to help identify and

minimise this influence.

Previously highlighted difficulties with recruiting young people successfully

for studies about foster care led to an anticipation that recruitment was

likely to be difficult in this study (Gilbertson & Barber, 2000), which would

have potential consequences for being able to saturate the data.

Therefore Willig's (2008) Abbreviated Grounded Theory approach was

adopted to enable development of a preliminary framework despite these

anticipated limitations. It ensures analysis goes beyond descriptive

accounts, though is more limited in its ability to broaden and refine the

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analysis through obtaining further data than a full Grounded Theory

approach2. It was hoped that this project would work as a 'foot-in-the-door'

study (Burger, 1999) developing understanding upon which to develop

and direct further research.

Ethics

The University of Surrey Faculty of Arts and Human Sciences Ethics

Committee gave a favourable ethical opinion for the study (See Appendix

A). The research was also undertaken in line with British Psychological

Society (BPS) and Health and Care Professions Council (HCPC) guidelines

(BPS, 2010; HCPC, 2012).

Inclusion & Exclusion Criteria

Inclusion criteria were broad, as an appropriate starting point for collection

of data in a Grounded Theory study. Some criteria aimed to contain the

parameters of exploration, given the small scale of the study. The

exclusion criteria mainly focussed on ethical considerations, to prevent

2 See limitation section for discussion of key limitations.

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inappropriate participation in the study from causing distress or harm.

Inclusion Criteria:

Young people who experienced a placement breakdown in foster

care after the age of 11 years, to avoid confounding placement transition

issues with school transition issues.

Young people 12-21 years of age. This ensured placement

breakdowns had been experienced after age 11 but also gave recent care

leavers an opportunity to share their views.

Young people who were in mainstream schooling. Interviewing

individuals with additional needs would have increased the likelihood of

engagement difficulties and the risk of emotional distress that could arise.

Exclusion criteria:

Young people who experienced a placement breakdown only in

kinship foster care, due to the different arrangements associated with this

form of foster care.

Young people currently receiving mental health support. This was to

avoid risking causing further distress to individuals potentially already

distressed.

Young people who had experienced a placement breakdown within

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the last six months or were at imminent risk of breakdown, due to the

increased distress or difficulties that could result from discussion of

placements.

Sampling strategy and recruitment

Given the historical difficulties in recruiting to studies regarding care

experiences, theoretical sampling of participants was anticipated to be

difficult. Due to time and resource constraints, selective sampling was

used, based on the inclusion and exclusion criteria.

A number of strategies were used to recruit participants used. This

included: using a social networking site, Twitter, to advertise to young

people directly and to charities and organisations working with young

people; emailing agencies and social service teams working with young

people in and just after leaving care.

In total 48 organisations were emailed. 108 followers on Twitter were

obtained, including organisational and personal accounts. On Twitter, one

young person was recruited from seven expressions of interest. Six further

participants were recruited, from a charity and two social care

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organisations.

As only seven participants were obtained it was not possible to be

selective in choosing which individuals to interview, limiting opportunities

to discover further concepts, variations among concepts and gain further

detail in relation to categories. Therefore the findings of this study remain

preliminary and tentative.

The process of recruitment ensured that participants had time to consider

their involvement. Professionals passed the study information to young

people, who then contacted the researcher directly to discuss the study

and consider participation. Young people on Twitter contacted the

researcher directly.

Recruitment methods aimed to reduce perceived pressure to participate

and facilitate young people to express their views freely. Consequently,

young people were only contacted directly if they initiated contact or

initial agreement to participate had been gained through associated

adults. Accessible information to obtain informed consent; time to decide

whether to participate; explicit opportunities to withdraw and to ask

questions were all elements which supported the non-pressurising

agenda.

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Careful consideration was given to issues of confidentiality, informed

consent and maintaining participant wellbeing. Participants could

withdraw from the study at any time. To manage wellbeing, the exclusion

criteria excluded individuals currently experiencing distress and after the

interview, written and verbal debriefs were given (Appendices B & C).

Follow-up contacts to monitor wellbeing were provided, with six choosing

to access this from the support worker or social worker, and one from a

direct follow-up contact with the researcher.

Participant characteristics

Seven participants aged 16-21 were included in the study: three females

and four males. Six were White British and one was Romany-Gypsy. Six

had left care in the last three years and one was just about to leave foster

care. Demographic details are in Appendix D. One potential participant felt

too nervous about participating and seven young people did not meet the

criteria.

Procedure

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Pilot interview and subsequent development of the interview schedule.

To ensure the interview questions appropriately supported the collection

of the young people’s perspectives on the research topic a consultation

with a care leaver was undertaken. This provided confidence that the

questions were clear and open and did not reinforce issues of power3 (See

Appendix E for the initial interview questions). Feedback resulted in the re-

phrasing of the questions: The term ‘placement breakdown’ was replaced

with ‘unplanned placement moves’,4 understood as placements ending

earlier than agreed in the child’s care plan (Rostill-Brookes et al., 2011).

The initial interview questions were broad to ensure participants were able

to raise the issues they perceived to be relevant. Additional interviews had

more specific questions that arose from analysis of the data after each

interview. (See Data Analysis section for further detail). (See Appendix F

for later interview schedule). For example, some of the early interviews

highlighted a reactive element to the experience of placement moves but 3 The intention was to support the young people to perceive themselves as an expert of their experience in the

interview. Therefore, using terminology that the young people associated with authorities over them or found oppressive or biased were removed.

4This term was preferred by the consultee as it was perceived as more common language and that 'placement breakdown' was a more research-based term. Though the terminology was changed in the interviews, unfortunately this consultation occurred after advertisement and therefore the language of the recruitment material reflected previously used terminology. The term was defined at the start of the interview.

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later interviews explored what determined or influenced this reaction.

(See Appendix G for example of how analysis contributed to interview

schedule). The broad questions were retained in the schedule to ensure

opportunities for further areas of relevance to arise in the interviews.

Although all seven participants had multiple experiences to report on,

analysis suggested that data saturation was not fully achieved. Some

areas of data appeared saturated. These tended to be those that had

arisen from the start and were discussed in each consequent interview, for

example the impact of support on the experience and appraisal of the

moves. However areas such as hopefulness (factors that influenced this)

and impact on biological family relationships appeared lacking in richness

and depth at the end of the process. Questions remained about these

areas and exceptions and disconfirmations were continuing to arise in the

last interviews.

Informed consent

All participants were aged over 16 and able to provide consent. Written

consent was obtained at the start of the interview following reiteration of

the study details. (See Appendix H & I for Information and Consent

sheets).

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Interviews

Six face-to-face interviews were undertaken. The seventh interview was a

phone interview at the request of the young person. The young people

chose when and where to undertake the interview. The interviews lasted

between 35 and 55 minutes and comprised demographic questions and a

semi-structured interview.

Data Analysis

The data were analysed using Willig's (2008) Abbreviated Grounded

Theory approach, based on Charmaz's (2006) full version. (See Appendix J

for a comprehensive description of the data analysis).

Each interview was recorded and transcribed verbatim by the researcher.

(See Appendix K for example of transcript and coding). Before the next

interview, transcripts were coded line by line to identify initial codes, using

the language in the transcripts to stay grounded in the data and limit

interpretation. These codes were built up into themes by identifying

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similarities and links between these to build theoretical codes. (To

maintain a stance that allows theories to emerge from the data, more

prescriptive elements of some approaches to Grounded Theory were not

used, such as ‘conditional matrices’ or an ‘axial coding paradigm’ (Strauss

& Corbin, 1990)).

Memos were used to explore questions and reflections that arose from the

coding process. This helped the researcher to identify gaps of information

(detail) to explore in future interviews. Theoretical sampling was also used

to help direct further comparisons within the data.

The memos also facilitated the researcher’s reflections on the data, to

help identify reactions, assumptions and biases that could lead data

collection and analysis in directions unintended by the young people. The

approach of the interview was to acknowledge the young people as the

expert of their experience. Clarifications and summaries were used to help

ensure the interviewer understood what was being shared by the young

people and reduce the influence of researcher assumptions.

Additional data from each interview enabled further exploration and

validation of the theoretical codes that were emerging from the analysis.

The aim was to help the researcher stay grounded in the data whilst

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developing a comprehensive understanding of concepts that would

facilitate movement towards theoretical integration and allow for the

development of a theoretical framework.

Theoretical credibility was built through ensuring analytical credibility,

using comparative analysis to build the initial and theoretical codes.

Despite not being able to be more selective about future participants to

expand on concepts and categories, systematic follow-up of elements in

future interviews aimed to improve theoretical credibility of the

relationships that emerged. However, the inductive approach of allowing

participants to choose the stories they shared before focussing in on more

specific lines of inquiry also helped to ensure additional experiences were

not overlooked in favour of identified gaps from theoretical sampling (Dey,

1999).

Following recommendations by Yardley (2000), supervision from a senior

researcher was used throughout the analysis in order to build and

maintain theoretical credibility, seeking guidance and feedback on the

emerging codes and framework. This input also provided a space for

reflection and transparency on the thought processes which influenced,

and were developed from, the data analysis.

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Results

The following model (Figure 1) represents what the young people said

about their move experiences, which centred around two main themes:

Understanding and Survival. The main theme of ‘Understanding’ contains

two subthemes of ‘Experience’ and ‘Support’. The ‘Survival’ theme

contains three subthemes of ‘Action to Influence’, ‘Self-protection’ and

‘Future Focus’. The two main themes influence each other. However, not

all the subthemes directly link to all others but are influential on a meta-

level to the other main theme and the subthemes within it. It is

emphasised that full saturation of the data was not achieved and

therefore these results may lack some additional relevant details.

Figure 1: Model of results

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Understanding of placement moves was constructed from appraisals of

past experience and influenced by the presence or absence of support.

Experiences used in these appraisals were those from both within care

and before care. 'Understanding' shed light on reasons for placement

move experiences and informed expectations of the future. These

informed survival responses subsequently. 'Survival' responses included

active strategies intended to influence events or self-protective strategies

to manage what was perceived as inevitable and hopeless (as informed by

the ‘Understanding’ of placement moves). Hopelessness was also

managed through a future focus on getting to the end of the care system.

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Reflecting on their experiences informed their understanding of the

moves, which influenced the actions taken to survive them. The results of

these actions impacted their subsequent experiences and support

received, which in turn influenced future understanding and survival

responses. This highlights the cyclical nature of the model. The main

purpose of this cycle appeared to be for the young people to reduce their

distress, particularly from loss and lack of support.

In the following sections the model will be illustrated by highlighting the

key elements and then drawing attention to the links between the themes

and subthemes.5,6

Understanding

Accounts of placement moves were predominantly highly negative. Loss

was highlighted as one of the most distressing elements of placements

5 Pseudonyms have been used to protect confidentiality. 6 Appendix M examples a finding evidenced by multiple interviews.

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moves, exacerbated by the fact that they were frequently multiple and

varied.

“Absolutely horrible. I was crying … I just felt like all my life was gone

between my feet.” (Amy)

The participants’ accounts emphasised their constant appraisals regarding

their placement moves. These appraisals informed some emotional

responses to the moves and expectations for the future.

“Why is this happening? These are the things that were going through my

mind. ‘What have I done that’s so wrong for me to deserve this?” (Lisa)

Key in influencing these appraisals were their experiences; both pre-care

and in-care. In addition, there was a clear emphasis on the influence of

support on their appraisals.

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Experience

Attempts to understand the events of placement moves were informed by

previous experiences: the young people drew upon their pre-care

experiences as well as prior experiences in care (if applicable).

“They don't really listen to you.…. So... they kind of do what they want

and put you wherever you are and you can't really control [any of what

happens].” (Rich)

Pre-care experiences influenced the young people’s sense of responsibility

around difficulties with placement moves. Those who entered care later

had a greater understanding of the responsibility of adults to provide care

for them and consequently attributed some of the responsibility for

difficulties with moves to the professionals around them. Anger arose from

perceptions that appropriate care was not being provided.

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Those who understood the responsibility of adults to provide appropriate

care adopted an active stance to influence these adults. They also felt less

guilt around the ‘disruptive’ behaviours used to achieve this.

In contrast, the participants who entered care at a younger age took

greater responsibility for difficulties associated with placement moves,

acknowledging difficulties engaging with the process and giving greater

credence to this as the reason for distressing placement moves rather

than to adults around them.

“…’ where do you want to live?’ ‘Well, I don’t really know. I don’t really

know what foster care is’... So a lot of the time I was just like ‘I don’t

mind”. (Rich)

Their own perceived failings led to a sense of hopelessness about being

able to influence future move experiences and a tendency to focus on

self-protection to minimise distress from future events.

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“I would love my choice to be increased but until I hit eighteen everyone's

always trying to tell me what to do because in their eyes I'm still a child...”

(Sian)

Other pre-care experiences had a more negative impact on the move

process. A common example of this was experiences of abuse creating

difficulties in young people’s abilities to communicate their needs or

dissatisfaction to those with power over their care. Such reflections only

occurred in their later years in care, resulting in an increased sense of

responsibility for difficulties with placement moves in the meantime.

“I never felt…able to say to my social worker what I wanted …if you relate

it to like my childhood, where I was abused... a lot of kids, they daren’t

say something… about their parent figure as they feel that they’re going

to get hurt.” (Jake)

This sense of responsibility and feeling unable to influence the situation

was linked to attempts to protect themselves from anticipated future

negative experiences, feeling unable to act to change these.

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“I got too attached and it really hurt when I left’… So I became very ‘to

myself’ and I was like … ‘I’m not gonna talk to [foster carers]’.’’ (Amy)

Experiences of being unable to make their needs known in care

highlighted that in-care experiences also influenced appraisals of

placement moves.

Information from previous experiences in care was used to understand the

actions of those influencing placement moves. For example, experiences

of being ignored by social workers when trying to make their views heard

or feeling their foster carers didn’t genuinely care about them were used

to understand why they felt unprotected and uncared for during moves.

“… I'd often overheard the stuff that [foster carer] would say like; 'Oh we

wish we'd never taken her on' and all of this... I came back one day and

[foster carer]’d packed my stuff and I just felt as if she was like, 'Yes, she's

going. Let's get rid of her'.” (Lucy)

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Such experiences consequently influenced expectations of future care

moves, for example that their wellbeing would continue to be overlooked

in favour of saving money and professionals could not be trusted to

behave otherwise.

“Participant: I was just so angry that my welfare… comes second to

money. Like, it might be a job to them, like having to move me and you

know, paying for it, but it’s my life.

Interviewer: Did that have any impact on you?

Participant: I didn’t trust Social Services… that was one.”(Adam)

A hopeless sense of future care and issues of mistrust of professionals and

foster carers were common and frequently followed by a sense of need for

self-sufficiency; the need to take action to survive placements moves.

“Social Services... they work to ensure my wellbeing. If they're not going

to work to ensure my wellbeing then I damn well am.”(Jake)

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Support

Young people felt repeatedly rejected and unwanted from the experiences

of moving placements and, with a lack of emotional and practical support,

felt alone and afraid. Lack of support and information given influenced the

conclusions around placement moves as young people frequently relied

on their own experiences and interpretations.

Positive support around understanding placement moves was uncommon

and frequently self-blame was experienced. This went beyond a

contextual conclusion regarding their behaviour to an integrated part of

their identity.

“Participant: I didn’t really have anyone talking to me about it, just,

‘You’re moving.’ … It really shocked me...What have I done that’s so

wrong for me to deserve this?

Interviewer: And what were the answers you came up with at the time?

Participant: I was naughty. I was a naughty person.” (Amy)

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The lack of perceived entitlement to good care that resulted meant that

such individuals attempted to survive care more often by taking personal

responsibility. They adopted self-protection strategies rather than acting

to influence others, even though these strategies could be harmful

(isolation, low mood, reduced access to support).

“I didn’t want to focus on my day-to-day life so…I learnt to block things

out...when I first went I didn’t know how to block so I just started trying to

hurt myself...because I thought I was to blame for everything that went

wrong in my life.”(Sian)

However, one young person displayed no self-protective strategies

despite a sense of responsibility around care moves, due to a more

prominent sense of hopelessness.

"I felt like ‘what’s the point in doing anything anymore,’ like, I started to

give up on myself.”(Lisa)

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Negative views of themselves also came from adults around them in care,

and influenced future expectations of their care. A particular sense of

hopelessness along with self-blame followed these incidents.

“They were like …‘You know no one’s going to want to foster you with

your referral, you know that.’ So… everybody knew that… no foster

placement would have me…”(Rich)

This profound sense of hopelessness was linked to attempts to self-protect

and place a sense of hope in the end of their time in care.

When positive support was received, the contrast in their understanding

and consequent emotional and practical responses was very evident. Such

support was often informative, empathetic and caring, providing both

instrumental guidance and also a mindful awareness of the young

person’s situation.

In addition, young people’s understanding of their moves facilitated

descriptions of what support would improve these experiences.

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“I think they should be allowed...they can keep in contact with them... it is

like leaving your family...It's really sad. It's traumatic.” (Jake)

Relational losses were repeatedly highlighted as the most distressing

elements of moves. However, young people emphasised that support

around this was only helpful when the professional (social worker, foster

carer, other professional) supporting them knew them well.

“... I met my Social …on the day that I left…She was trying to comfort me

because I was upset and I felt a bit... I felt a bit like she was

intruding...”(Lucy)

Positive support reduced the need to self-protect, providing emotional

support and confidence to influence placement moves. Initially it also

appeared that positive support relieved a sense of responsibility around

placement moves.

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“My CAMHS worker said to me, ‘It’s not because you’re naughty, it’s

because people don’t understand you.’ And then, that’s how I figured out

that they obviously don’t understand me.” (Sian)

However on exploring this in consequent interviews it became apparent

that regardless of previous experiences, and whether they had fostered a

sense of self-value, all participants appeared to feel some sense of

responsibility for the difficulties they experienced around placement

moves. When combined with a lack of support, this perception of

responsibility led the young people to articulate that they had to survive

by being self-sufficient as no one else would prioritise their emotional

needs.

“… if I hadn't had that, like the strong will to do what was best for me and

been articulate enough to tell everybody that that was what I wanted and

been determined enough to fight for it, then I probably wouldn't have

gotten what I needed.” (Lucy)

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However, this was the only participant to indicate that they felt they had

got some of their needs met. Others indicated that their actions had only

reduced distress.

Relational losses were often of those who were supporting them, whether

carers, biological family or friends. This reinforced the need for self-

sufficiency to protect against these significant loss experiences. They

invested less in these relationships as a self-protective device, which also

reduced opportunities for future support to manage other distresses.

“Cause I could have got closer to them…and it could have hurt me a lot…

I was like, ‘No. I’m gonna cut all the ties…and not talk to any of

them.”(Amy)

Overall, the young people’s ‘understanding’ of placement moves

frequently led to a conclusion that they needed to be self-sufficient to

manage the distress resulting from placement moves and to minimise

anticipated future distress. This came from a pervasive lack of support

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during the moves, throughout and prior to care. The young people’s

careful appraisals of placement moves influenced their beliefs around self,

others and the future. These consequently informed their ideas about how

to manage future experiences: how to survive placement moves.

Survival

As highlighted previously, whilst in care the young people’s understanding

of their placement moves informed their survival responses; these centred

on managing their current distress, and future anticipated sources of

distress, and fell into three themes. ‘Action to Influence’ aimed to

influence future events to negate distress whereas ‘Self-protection’ aimed

only to limit the negative impact of what they were to experience. The

third theme, ‘Future Focus’ centred on hope for the future. A focus on self-

sufficiency was prevalent in all these themes, a clear result of the lack and

loss of consistent support leading young people to depend on themselves.

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“I would have been incredibly unhappy….But I wanted to fight for what

was best for me rather than just…having adults tell me what to do.”

(Adam)

These attempts at ‘survival’ influenced future experiences: how the

participants engaged with support; how they viewed their placement

moves; their subsequent approach to surviving the experience. This

illustrates the cyclical nature of the process whereby experiences and

evaluations affected actions, which in turn influenced experiences and

evaluations and so on.

What was clear was the ‘no win’ situation the young people found

themselves in, with attempts to reduce distress often creating alternative

distress. A focus on the future after care provided a hopeful outlook in the

midst of these dilemmas. Initially, the descriptions of survival responses

appeared to be an ‘either/or’ scenario regarding the use of actions to

influence. However further exploration in subsequent interviews identified

that some young people engaged in both of these response approaches

during a move. For example, they refused to engage with foster carers to

reduce distress but also ran away from placements to influence their

move.

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Less-distressing experiences were appraised as requiring fewer survival

responses. For example, young people who felt known by, and who

trusted, their social workers were more accepting and less anxious of the

placements chosen for them. They did not feel the need to run away from

or refuse these placements (at least initially).

“I could really tell how excited she was for me and that got me excited,

‘cause I was like ‘[she] knows me really well and I’ve got a good

relationship with her.” (Rich)

For these young people there was less of a need to be self-sufficient,

giving more opportunities for their needs to be met by others and

reinforce the benefits (and drawbacks) of this. In contrast, some of the

young people were clear that the lack of positive support compromised

their success in placements.

“…you know if they'd have said ‘you're here for so long’…then I could

have taken that in and gone ‘ok, I know my time here is limited’ I think I

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would have been a lot calmer... and stood a good chance of staying in the

placement.”(Sian)

However some responses were reactive rather than based on appraisals

of the moves, such as becoming aggressive towards their social workers

during the process of being moved. The young people then thought about

the consequences of these actions and used these appraisals to decide

whether to act the same way again in future.

“...That move was obviously immediate ‘cause I ran away to my dad’s…

But then it changed...‘Cause the reason I [would] run away was …would

be a lot of the time because I wasn’t being listened to.”(Rich)

Action to Influence

For some young people there was a motivation to survive and reduce

distress that culminated in actions to achieve their desired improvements.

Attempts to influence moves often focussed around the high level of

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distress associated with loss of relationships. Actions were intended, for

example, to obtain better support from the social worker.

Actions were often aimed at those whom they perceived had control over

their placement moves: Social Services, foster carers, etc. They included

direct negotiations regarding placement moves, ‘kicking off’, running

away and refusal behaviours. Attempts to influence those in ‘control’ also

included gaining support from other professionals to oppose a move.

“...She... listened to my Psychiatrist and listened to me… she overruled

everything that [the social worker] said and I managed to stay in the

place...” (Amy)

Whilst young people’s actions to influence were generally meant to create

positive change, they had mixed results. In fact, a key negative

consequence of some behaviours intended to influence moves was the

negative perception of the young person that resulted. This was part of a

context of experiences of negative perceptions of young people in care

that was prevalent in the accounts: actions that risked reinforcing these

were heavily justified. For example, one young person attributed their

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‘kicking off’ to their mum’s emphasis that they should fight to get their

needs met, thereby reducing their sense of shame at being aggressive

towards their social worker.

“My mum raised me …that I was... like, responsible for my own

wellbeing.”(Sian)

Such examples repeatedly highlighted that the need to be self-sufficient

rarely provided the young people with ‘ideal’ solutions to reduce future

distress, and frequently resulted in cognitive dissonance. The individual

from the quote above believed she was of value and entitled to receive

good care but did not perceive she was receiving this. To resolve this, she

ensured she gained the care she needed by ‘kicking off’ to get those

around her to listen and respond to her requests. Though this succeeded,

further cognitive dissonance arose from her perceiving herself as a ‘bad

person’ that conflicted with her belief that she deserved good care. This

reinforced her need to justify herself, both whilst in care and afterwards to

manage this dissonance. The need to continue to justify herself in the

present highlighted the on-going fear of being perceived negatively, that

had started in her childhood and not yet been resolved.

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However, though some behavioural responses proved effective at

influencing individuals and circumstances, ineffective behavioural

responses engendered a sense of hopelessness and led to an alternative

approach of self-protection from the perceived inevitable future

difficulties. An exception to this was one young person, who became self-

protective before her first move, following failed attempts to engage

foster carers in fighting for her to be allowed to stay in the placement.

Self-protection

Young people with greater perceptions of hopelessness and self-blame for

the difficulties with moves engaged in more self-protective strategies. This

was also reinforced by previous failed attempts to influence placement

moves. The intention of these behaviours was to minimise distress, most

frequently around relationships and loss. This included denial at the loss

of relationships as well as reluctance to engage in new relationships.

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“I didn’t wanna…make new friends ‘cause I already had friends over here.

So I didn’t really wanna go out and make a new circle of friends and end

up losing them again...” (Lisa)

Although these self-protective responses were perceived to be somewhat

effective at reducing future hurt, the young people acknowledged that

they often brought with them isolation and depression. This further

reduced opportunities to obtain support, leading to further hopelessness

and reinforcing the need to engage in self-protective behaviours.

“I become really depressed. I didn’t want to go out. I didn’t talk to

anyone.” (Lucy)

The dissonance caused by these negative outcomes was resolved by

some of the young people justifying that these experiences made them

emotionally stronger.

“It’s made me stronger.…. I don’t think anyone else realizes how strong it

actually does make young people.” (Jake)

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Acceptance of acting to survive as best they could was common

throughout the narratives, though disruptive and aggressive behaviours

were often discussed with a sense of embarrassment. However an

exception to this was one young person who expressed ongoing regret at

engaging in self-protective approaches: She felt that had she ‘acted to

influence’ those in charge of her care that she would have avoided the

depression and consequent educational failures that she attributed to

taking a self-protective approach. This perspective existed despite an

acknowledgement of the hopelessness that had led her to take a ‘self-

protective’ approach.

“I definitely think … I don't want to sound like I wanted to cause trouble…

I should have fought my corner more. But yeah, I just never said: I just felt

so on my own like no-one would listen to me at all.” (Sian)

An acknowledged positive outcome of self-protective behaviours for all

the young people, was the avoidance of shame often associated with

more active and disruptive strategies, stereotyped to be common

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amongst young people in care. This reinforced their use in future care

moves.

Future Focus

Another approach utilised by the young people was one of focussing on

life beyond care; hoping that life would improve after care. The young

people identified their time in care as a discrete chapter in their lives,

enabling them to be hopeful about the future; a time beyond the trials and

tragedies of care. Reflections after care maintained this perception of care

as a discrete chapter that impacted on their achievements and successes,

and continued to limit their lives.

“[Social workers] did whatever they [wanted]…I just went along with it

and then as soon as I was independent…I was like ‘…It’s time to get all

the things I’ve wanted to do.’ So it was quite a relief...”(Rich)

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This focus on the future enabled individuals to separate themselves from

the behaviours they had engaged with in care and give the care system

responsibility for this, rather than perceive themselves as fundamentally

‘bad’. However narratives contained repeated emphasis on this

separation, highlighting an on-going fear of being perceived negatively as

a child in care.

“I'm not violent now or nothing like, I’ve left it behind” (Amy)

Despite the acknowledged difficulties and distresses with placement

moves, the young people all perceived themselves as survivors, though

acknowledging some of their on-going difficulties as a result of these

experiences.

“It’s in the past and I’ve tried to keep it that way. To be reminded of it.. It

makes me feel …quite low about myself. .. I mean I’ve made myself the

person I am today… It’s made me stronger... I don’t think anyone else

realizes how strong it actually does make young people.” (Jake)

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What was clear across the narratives was a sense of survival and relief at

leaving care, or hopeful anticipation of it for those still within the care

system. However, what was unclear was the extent to which negative

perceptions about themselves were concealed, in a wish to distance

themselves from the ‘bad’ image of a child in care.

Within the overall theme of ‘survival’, the majority of the young people

engaged in both active and self-protective strategies, rather than just one

or the other. Switching most commonly occurred from active to self-

protective strategies, as actions to influence failed or hope around better

experiences and support disappeared. However, alongside

acknowledgement of the insufficiency of these approaches to prevent

future distress, the young people highlighted the double bind they were

caught in: act to improve their situation and risk being stigmatised

further, or focus on protecting the self and risk isolation and depression.

In summary, the results of this study indicate a cycle of appraisal and

response in relation to placement moves, to reduce distress. Placement

move experiences were appraised and informed consequent responses,

which then influenced placement moves and led to further evaluations to

inform future responses. Sometimes losses were averted and support was

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provided through these responses, but often responses came with

drawbacks as well as successes. The need for self-sufficiency indicated in

the appraisals led to responses that often furthered isolation and reduced

opportunities for support that could have relieved distress. Consequently,

further distress from multiple placement moves led to a sense of

hopelessness and the young people ‘survived’ this by focussing on their

future beyond care, as they recognised their needs but were unable to get

them met sufficiently.

Discussion

This study aimed to explore the process and impact of placement moves

from the perspective of young people in foster care to develop a

preliminary foundation of understanding regarding the psychological

processes and behaviour related to these perspectives. It was intended

that this work would function as an early platform for other researchers to

further develop a coherent and theoretically-based account of these

phenomena, to inform effective and evidence-based interventions.

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The themes to emerge from the data highlight the attempts of young

people to understand and survive these experiences in order to manage

their distress and minimise the development of future trauma. In their

reflections, they were mindful of the impact of these experiences on their

lives, with the consequential benefits of acquired resilience as well as the

considerable difficulties. The landscape was filled with multiple losses,

with a backdrop of lack of information, uncertainty, and lack of support.

The themes of understanding and survival encapsulate the young people’s

process to manage their experiences. Their ability to recognise their own

and others’ contribution to the systemic problem of the moves was

articulated in multiple layers focussing on economic, emotional and social

values.

This discussion will explore how the results of this study fit with

theoretical models and previous research with young people in care,

highlighting areas that require further exploration or indicating areas for

intervention within care services. Theoretical models focussed on will

include trauma, learning, attachment and resilience. These models have

been included due to their relevance to the results. Other theories have

been rejected due to a lack of congruence with the results. For example,

psychoanalytical developmental models have not been included here due

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to the lack of evidence in the results to substantiate such congruence or

divergence of the findings of this study with such a theory7.

Resolving Trauma

The narratives in this study clearly fit with the criteria for Developmental

Trauma (Van der Kolk, 2005) (Figure 2), drawing into sharp focus that

instead of providing nurturance, care system moves played a role in

maintaining and exacerbating early trauma that young people often bring

with them into care (Takayama, Wolfe & Coulter, 1998). Secure bases,

necessary for the development of attachments and sustaining

relationships, were lacking. Such experiences explain the young people’s

need to ‘understand’ and ‘survive’ placement moves and indicate a need

for trauma-based support.

Figure 2: Developmental Trauma

7 Appendix N examples a search based on the result

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Advocation of trauma-based support for young people in care is not a new

idea (Hyde & Kammerer, 2009; Thomas & Philpot, 2009; Webb, 2006;

Cairns, 2002). For example, Hyde & Kammerer advocated trauma-based

support for young people after finding that young people brought

behaviours resulting from their trauma to placements, that carers were

then unable to manage, resulting in further breakdowns. The results of

this study advocate the implementation of such support, given the

findings that placement moves themselves were traumatic and resulted in

behaviours to reduce associated distress that then risked increasing

further trauma from additional moves.

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Fight, Flight or Freeze

The results also highlight the stress response of the young people. Though

their attempts to ‘survive’ placement moves were attributed mainly to

appraisals, the narratives indicated the stress response present in these

experiences. For example, the ‘flight’ of the young man to his father’s

house at the threat of being moved. Though this later came to be a

strategy of influence for him, it indicated the trigger of the stress response

during moves. Younger children are less able to engage in ‘fight’ and

‘flight’ strategies and therefore more frequently engage in ‘freeze’

(Lowenthal, 2012). In addition to having a reduced sense of entitlement to

care, this may shed further light on why children who entered care at a

younger age engaged with professionals in charge of moves by actions

such as becoming emotionally unavailable (freeze). Such inferences are

supported by previous propositions about foster children’s responses to

psychological stress (America Academy of Paediatrics (AAP), 2000).

Understanding New Worlds

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The narratives highlight that placement moves were often a learning

process for the young people: they did not know what to expect from the

moves initially and consequently often had to piece together information

and experience themselves to make sense of them. Their conclusions

then informed their responses (particularly to manage distress). Often, the

stress responses undertaken in the immediate moment were also retained

in the considered responses: aggression and running away (fight and

flight) were associated with ‘action to influence’ whereas withdrawal

(freeze) encapsulated self-protective strategies. Stress impacts the ability

to learn (Thompson, 2014) and it may be that this chronic and ongoing

stress limited the effective appraisal and response decisions for the young

people in regard to their placement moves.

However the responses often increased the distress of the young person.

For example they withdrew from relationships to avoid further loss but

also missed out on support. These unsuccessful actions to reduce distress

can be understood in the context of a learning process: children try to

make sense of tasks and experiences (identify the meaning of them) and

errors occur when social contexts are unfamiliar as the young person has

no framework or scaffold to inform their actions (Donaldson, 1984). The

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lack of framework for placement moves highlighted by the young people

in this study emphasises the ‘disembedded’ thinking of the young people

and helps to understand their difficulties in comprehending and

responding to their experiences in a way that benefitted them.

Errors due to a lack of framework highlight the dependency on adults

around them to help them navigate unfamiliar situations successfully by

providing information from a ‘child perspective’ (Donaldson, 1984) in

order for young people to appraise situations correctly and respond

constructively. Local and national approaches support this principle of

including young people in decisions about their care (Wright, Turner, Clay

& Mills, 2006.), but it is employed to a limited extent according to this

study’s participants. The on-going lack of support and the reactive nature

of the placement moves prevented preparation or meaningful discussion.

Consequently dysfunctional scripts were not corrected and young people

continued to respond in ways that compromised their future needs being

met.

Attachment and Emotion Regulation

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The participants described a lack of support and consistency of

relationships, alongside distress from loss, feelings of abandonment and

associated vulnerability. These are consistent with the emotional

responses expected when an individual has experienced insecure or

disorganised attachments (Prior & Glaser, 2006). Such attachments are

prevalent in young people who have been fostered, due to trauma in pre-

care attachments and/or during care (Wekerle & Wolfe, 1998; McCarthy &

Taylor, 1999; Crittenden & DiLaila, 1988). However the youth in this study

highlighted how their experiences of relationships around placement

moves (rejection, lies, absence of support when needed) influenced their

ability to engage in relationships with those caring for them. Lack of trust

and repeated loss of relationships led to distrust and perceptions of ‘carer’

relationships as harmful and to be protected against, which were

characteristics of young people in care also found by Unrau et. al. (2008).

This suggests a process by which insecure or disorganised attachments

may be exacerbated by care events.

Developed by Bowlby (1951), attachment theory proposes that the

relationship between infant and mother forms the basis of a sense of

security for the infant, informs emotional development and future

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relationships. Further work distinguished privation (no attachments

formed) from deprivation (loss or damage to attachments) (Rutter, 1981;

Hodges & Tizzard, 1989). The need to self-protect against relationships,

thereby reducing opportunities for attachment relationships to develop

highlights how foster care can increase this risk of privation.

Moderate difficulties with affect regulation during the interviews also drew

attention to attachment difficulties (Fahlberg, 1991), given that emotional

regulation develops through secure attachment relationships. For many of

the young people, their emotions appeared disorganised, unregulated,

absent or masked. Strategies to manage these difficulties included

suppression, minimising or dismissing their experience of emotions,

changing the topic and actively stating this was in the past. Emotional

regulation is adaptive for helping young people achieve their goals and

fostering a positive sense of self, a characteristic largely absent in the

young people in this study, despite efforts to conceal difficulties in the

present time.

Though the need for positive, stable relationships in order to facilitate

secure attachment in foster care is acknowledged in theory, research and

practise, implementation appears to remain problematic (Luke & Coyne,

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2008; Samuels, 2009). Given the development of secure attachments will

not only significantly reduce distress and instability in care (through

preventing harmful self-protective or active strategies) but also improve

multiple outcomes beyond care, associated with secure attachment

relationships (Prior & Glaser, 2006), this needs to be a priority.

Internal representations

Rather than their placement moves being conceptualised as the result of

specific externally driven factors, the young people related them to

internal global attributions which impacted on the development of their

self-identity. In light of the loss of relationships and role models early in

life it is unsurprising that many of the young people had poorly-attuned

internal working models (IWMs), demonstrated by the way they viewed

themselves and others. Bowlby (1973) explained that mental

representations of the parent-child relationship, built through interactions

with primary caregivers contain expectations of caregiver behaviour in the

future, such as availability or responsiveness. They also contain a

‘complementary and mutually confirming view of the self as worthy or

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unworthy of care’ (Bowlby, 1973 p, 238). Clear negative examples of this

came from participants in this study: unavailability or rejection from

carers and professionals and consequent insecurity and lack of trust led to

self-reliance for care needs and a negative sense of self, occasionally

partially negated by positive experiences of care and support. Kools

(1997) and the AAP (2000) emphasised the negative impact of foster care

on the development of young people’s identity, resulting from poor

treatment from professionals around them.

Resilience

Within this study the focus on survivorship of the traumatic experiences of

placement moves indicated resilience. Newman and Blackburn (2002, p3)

describe resilient children as ‘equipped to resist stress and adversity,

cope with change and uncertainty, and to recover more successfully from

traumatic events or episodes’. Originally described by Rutter in 1990,

resilience is a dynamic process of managing experiences of adversity and

learning how to adapt and accommodate to these life challenges to

achieve effective adult adjustment (Luther, Cicchetti & Becker, 2000).

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Resilience in young people in foster care has gained great attention in

recent years, given the ability of some young people to achieve

favourable outcomes despite the traumatic experiences of their lives prior

to and within foster care (Cameron, 2007; Pryce & Samuels, 2010; Wilson,

Sinclair, Taylor, Pithouse & Sellick, 2004).

In this study, survival often took the form of self-reliance, as the young

people took it upon themselves to address their emotional needs by

reducing distress from moves. This finding was also ascertained by

Samuels and Pryce (2008) who explored reflections of young people

ageing out of foster care. As in this study, they also identified that whilst

self-reliance could be a source of resilience it could also interfere in

accessing and developing supportive relationships associated with

positive outcomes in adulthood.

The young people who retained optimism highlighted problem-solving

skills, maintained a sense of autonomy over their situation and engaged in

more hopeful responses to improve their situation. These are three of four

attributes of resilient children highlighted in research by Bernard (1995)

and ascertained to be factors related to positive outcomes in young

people in foster care (Edmond, Auslander, Elze & Bowland, 2006; Hass &

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Graydon, 2009). However within this research, optimism often appeared

to be influenced by sense of autonomy and positive sense of self,

highlighting an area to be explored further.

A focus on the future was one method of survival identified by the young

people, alongside attempts to reduce distress. AAP (2000) highlighted that

adults cope with impermanence by building self-reliance and focussing

and preparing for a time of greater constancy, an approach that appeared

to be adopted by many of the young people in this study and facilitated

their resilience.

A distinction between life in care and after care enabled young people to

separate themselves from previous ‘bad’ behaviour and retain (or

develop) a positive sense of self. The majority of the young people

interviewed reported improvements in mood, behaviour, relationships and

achievements after care, despite the intense difficulties experienced

previously. It is unclear what facilitated this resilience. However, all of the

young people reported one key positive source of support (usually not

linked to care services) before, during or after care. One main positive

source of support was identified as a key factor in resilience for children

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by Newman & Blackburn (2002) and supported in consequent research,

highlighting the significance of this.

A few young people who entered care expressed some entitlement to

having their needs met. This appeared to be associated with greater

resilience to care move events as they internalised less responsibility for

difficulties with care moves. Such findings suggest that these individuals

entered care with an (at least partly) positive IWM (though the majority

did not). These were the young people that entered care later, having had

time to develop these (AAP, 2000). This indicates that positive IWMs may

potentially be a source of resilience for young people in care and

highlights the consequent need to facilitate these.

Resiliency theory highlights the important of having some autonomy or

knowledge over the breadth of changes occurring, in order to be able to

prevent these experiences hindering young people’s development

(Newman & Blackburn, 2002). Young people themselves were aware of

specific elements of support that could have reduced the trauma of

moves. For example, social and contextual factors such as having a

trusted consistent relationship with an adult, knowing what to expect,

being able to prepare for moves and having some control to ensure the

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decisions taken met their needs. Therefore this study supports other work

which challenges the exclusion of young people from decisions and

information, not just to reduce distress but to aid development of

resilience. In addition, the alignment of the young people’s identification

of their needs with theory about resilience adds weight to the argument to

listen and respond to young people individually: they can be accurate

experts of their needs.

Areas for intervention

Despite the tentative nature of the findings of this research, through the

triangulation of the findings with theory the need to address support for

trauma, attachment, resilience and emotional regulation in placement

moves has been indicated. However, much of this fits with the work being

undertaken by those such as Golding (2004; 2007; 2008; Golding &

Hughes, 2004.) and Hughes (2004; 2006; 2007, 2009.) to develop

approaches to address trauma and attachments in young people in care.

Further evidence for the effectiveness of these approaches is still required

to justify broader implementation.

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Limitations

This study aimed to explore young people’s experiences of UK foster

placement moves. The applicability of this research is limited by the

restricted variation in the participants’ ethnic, cultural and social

backgrounds. These are important elements given that in the UK, African

Caribbean and mixed African Caribbean and white heritage children are

overrepresented in foster care (Thoburn, 2007) and locations such as

Scotland have care systems run by their own government.

A greater number of participants may have led to a greater depth and

breadth of information around the process of managing placement moves.

It may also have facilitated fuller saturation of the data, which has

consequently rendered the results a preliminary understanding of

placement moves. However, participants’ experiences of multiple moves

at least partially compensated for the small number of participants.

Furthermore, though general guidelines suggest numbers of 20-30

participants for Grounded theory studies (Charmaz, 2006; Creswell, 1998)

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justification of these numbers is lacking. Guest, Bunce and Johnson (2006)

found that they had generated 34 of their 36 codes within the first six

interviews of their study, with all 36 generated by interview 12. This also

suggests the small number of participants may not be as significantly

limiting as may first appear. The small number of participants also

prevented theoretical sampling which may have rendered data more fully

saturated with a small number of participants.

Conclusion

This research has enabled the development of a preliminary

understanding of the key elements of placement moves from the ‘child’s

perspective’. It has highlighted the process used to inform young people’s

attempts to survive the often-traumatic experiences of placement moves:

past experiences inform future expectations and consequent responses to

minimise future distress. Frequently a lack of support compounds the

trauma of placement moves and results in a need to be emotionally self-

sufficient. However, these self-sufficient responses often have a negative

impact on distress and stability.

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It is acknowledged that these results require further exploration to obtain

further understanding of factors that influence resilience and distress from

placement moves. However, the findings of this study support current

attempts to develop and evaluate interventions to: facilitate consistent

and positive relationships; aid the young people in development of

resilience; and manage and reduce trauma in foster care. Despite the

largely negative descriptions of care moves, this study has highlighted the

pervasively resilient nature of young people in care. But this must not be

an excuse to overlook the shortcomings of care.

The present research has also found that (at least some) young people

are able and willing to report on difficult experiences from foster care.

This emphasises that there is no excuse to neglect a ‘child’s perspective’

in research or in practice.

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Tapsfield, R., & Collier, F. (2005). The cost of foster care: investing in our children's future. London: British Agencies for Adoption and Fostering/ Fostering Network.   Thoburn, J. (2007) Globalisation and child welfare: Some lessons from a cross-national study of children in out-of-home care. Norwich, UEA Social Work Monographs.  Thomas, M. & Philpot, T. (2009). Fostering a child's recovery: Family placement for traumatized children. London: Jessica Kingsley.

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Thompson, R. (2014). Stress and child development. Future Child, 24, 41-59.

Unrau, Y. (2007). Research on placement moves: Seeking the perspective of foster children. Children and Youth Services Review, 29, 122-137.  Unrau, Y., Seita, J. & Putney, K. (2008). Former foster youth remember multiple placement moves: A journey of loss and hope. Children and Youth Services Review, 30, 1256-1266.   Van der Kolk, B. (2005). Developmental Trauma Disorder: Toward a rational diagnosis for children with complex trauma histories. Psychiatric Annuals, 35, 401-408. 

Webb, N. (2006). The impact of trauma on youth and families in the child welfare system. In: Webb, N. (Ed.), Working with traumatized youth in child welfare (pp. 13-26). New York: Guilford Press.  Wekerle, C., & Wolfe, D. (1998). The role of child maltreatment and attachment style in adolescent relationship violence. Developmental Psychopathology, 10, 571−586.

Willig, C. (2008). Introducing qualitative research in psychology. England: Open University Press.   Wilson, K., Sinclair, I. & Gibbs, I. (2000). The trouble with foster care: The impact of stressful events on foster carers. British Journal of Social Work, 30. 191-209.  

Wilson, K., Sinclair, I., Taylor, C., Pithouse, A. & Sellick, C. (2004) Fostering success: An exploration of the research literature in foster care. Social Care Institute for Excellence.  Wright, P., Turner, C., Clay, D. & Mills, H. (2006). The participation of children and young people in developing social care. Practice guide 6.

Yardley, L. (2000). Dilemmas in qualitative health research. Psychology and Health, 15, 215–228.

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Appendix A: Ethics Approval

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Appendix B: Debrief Statement

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Thank you for your help with this study. Here is a debrief sheet that has my contact details if you have any further questions that you would like answered about the study or decide you would like a copy of the report that I produce when I have completed the study. I would also like to call you a in a few days to ensure that you are ok from having discussed these difficult topics today. May I ask how you are feeling after the topics we discussed today...? What support or what do you think may be helpful for you after today…?

Thank you again for your help with this study.

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Appendix C: Debrief sheets

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Debrief Sheet: Young Person

A study of the experience and impact of foster placement breakdowns: the young people in foster

care’s perspective

Debrief

This study has investigated how individuals who experienced breakdowns in foster care placements viewed these situations and their views on what support they felt helped or didn't help during these experiences.

Placement breakdowns are often difficult experiences. Research in the past has asked foster carers and social workers about the experience but not young people in foster care and young people. This was sometimes because they did not want to upset young people by talking about these sad or difficult changes in foster care. This study aimed to ask your views in order to help services understand how to support you and other young people in foster care better during these times.

We are very grateful for your help with this study and being willing to talk about possible difficult memories. If taking part in this research has made you feel upset you may wish to talk to someone further. You could contact one of the following organisations for support by telephone or online via email.

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Childline 0800 1111http://www.childline.org.uk/Pages/Home.aspx

The Samaritans 08457 90 90 90 [email protected]

Support Line 0208 554 9004 [email protected]

Alternatively, if you feel very upset you should speak to your foster carer or social worker who may take you to your GP to get some more support.

This website also has information for young people on mental health and feeling well emotionally: http://www.youngminds.org.uk/

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Debrief Sheet: Young Person (18+)

A study of the experience and impact of foster placement breakdowns: the young people in foster

care’s perspective

Debrief

This study has investigated how individuals who experienced breakdowns in foster care placements viewed these situations and their views on what support they felt helped or didn't help during these experiences.

Placement breakdowns are often difficult experiences. Research in the past has asked foster carers and social workers about the experience but not young people in foster care and young people. This was sometimes because they did not want to upset young people by talking about these sad or difficult changes in foster care. This study aimed to ask your views in order to help services understand how to support you and other young people in foster care better during these times.

We are very grateful for your help with this study and being willing to talk about possible difficult memories. If taking part in this research has made you feel upset you may wish to talk to someone further. You could contact one of the following organisations for support by telephone or online via email.

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The Samaritans 08457 90 90 90 [email protected]

Support Line 0208 554 9004 [email protected]

Alternatively, if you feel very upset you may wish to speak to your GP for some further support.

This website also has information for young adults on mental health and feeling well emotionally: http://www.mind.org.uk/

If you have any other questions about this study you can contact me or my university supervisor. Our details our listed below.

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Appendix D: Participant Demographics

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Table 1: Participant Demographic Information

Participant

Age Gender Ethnicity

No. of foster

placements (not

residential)

No. of placements

after (moved into) 12 years

of age

Still in Care

1 20 Male White British

Multiple 2 No

2 19 Male White British

2 2 No

3 21 Male White British

9 6 No

4 20 Female White British

2 2 No

5 19 Female Romany-Gypsy

2 1 No

6 17 Female White British

3 3 Yes

7 17 Female White British

1 1 No

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Appendix E: Initial Interview Schedule

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Initial Interview Schedule

1) I wonder if you could tell about one of your placements where there was an unplanned ending? (about what happened when it ended?)2) Could you tell me about what happened next? (In terms of going to your next placement)?3) Can you tell me what it was like when your placement was ending/ ended?

These were broad initial prompt questions that were intended to get the interview started, build rapport and lead to a focus on the experience of the placement breakdown and consequences /impact/views on this. Further questions followed the young person’s lead in relation to these issues, feelings and experiences they highlight in relation to the placement breakdown from their perspective in line with Willig’s (2008) Abbreviated Grounded Theory Approach.

Interview were then transcribed and analysed, identifying key elements and components to explore further that then impacted the schedule of future interviews as they were prioritised and explored further. This process was in line with Willig’s Abbreviate Grounded Theory approach (2008).

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Appendix F: Later Interview Schedule

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Later Interview Schedule

1. I wonder if you could tell me about one of your placements where there was an unplanned ending? (about what happened when it ended?)2. Could you tell me about what happened next? (In terms of going to your next placement?3. Can you tell me what it was like when your placement was ending/ ended?4. What did you know about what was going to happen when you moved? How did you find this out?5. Why do you think the move process happened like this / this way? How did you understand what happened6. How did you react/respond to what happened? Why?7. Can you tell me about your other placement moves when the placement had an unplanned ending?8. (If any,) what was the impact of these experiences?9. What did you expect in future placement moves? Why do you think you expected this?10. Can you tell me what was important to you when you moved placements and why?11. How do you think placement moves should be done? / What do you think should be done differently?

NB: These questions were often not asked in an ordered and structured way; sometimes the answers came up in discussions about the process and were offered without being directly asked. Sometimes questions were repeated within an interview in relation to different placement moves experiences.

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Appendix G: Example of analysis producing interview schedule changes

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Example of transcript analysis:

Limited explanation

Go immediatelyLiving out of black bin bagsNo hope in permanency

No stabilityNo securityAlways ready in case

Fear of losing things

Confidence knocked

Constantly settling and moving

Impact on now – difficulty settlingUsed to play on mind

No, they'd just show up

Yeah. Pretty much (go immediately)I was living out of black bin bagsIt got to pointwhere I literally didn't even bother taking my clothes out of the bin bags or anything like that.‘cause I knew that I'd be… I could go at any timeso was just a case of keep my stuff in there,where I can just grab it

it's knocked my confidencebecause, I’d settle down somewherethen you get moved again.You settle down again, you get moved again,it just is like a vicious circleIt’s why it's like now, why I find it hard to settle init’s not always in the back of my mind nowbut it was a few years agolike, I know I'm going to move again soon

Participant: They'd just say, ‘oh you're going

to a new place’.

Interviewer: And did you get much warning?

Participant: No, they'd just show up.

Interviewer: Oh okay, and then you'd go

with them immediately?

Participant: Yeah. Pretty much. I was living

out of black bin bags. It got to point where I

literally didn't even bother taking my clothes

out of the bin bags or anything like that.

‘cause I knew that I'd be… I could go at any

time and so was just a case of keep my stuff

in there, where I can just grab it.

Interviewer: Okay, so you just started living

as if they were going to turn up any time?

Participant: Yeah

Interviewer: And how do you think that kind

of affected you, kind of thing?

Participant: Well, it's knocked my

confidence. Just because, I’d settle down

somewhere and then you get moved again.

You settle down again, you get moved again,

it just is like a vicious circle. It’s why it's like

now, why I find it hard to settle in, cos it’s, it’s

not always in the back of my mind now, but it

was a few years ago, it was in the back of my

mind like, I know I'm going to move again

soon........

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Associated memo – written after initial coding:

***** seems to be really impacted by this constant moving and lack of preparation for doing so. I wonder if others also experienced this lack of warning in moving and the effect it had on them – how did they respond, does it still affect them as it does *****. For ***** it seemed that he took on looking after himself in relation to being prepared to move, a kind of independence and I wonder if others responded the same or differently. There is a great protectiveness over his items that he also mentioned earlier in the interview and this process triggered risks of losing his items as well as reinforced beliefs that he would be moved without warning repeatedly. There is a sense that he has to look after himself and his belongings, given this lack of information (warning) about moving. I realised I did not ask if he felt not unpacking his belongings had any effect on the placement he moved to and I wonder if I felt nervous to ask too many questions about this particularly emotional and distressing part of the account for him. I wonder if others responded in this practical way of not unpacking their items if they perceived they would always move. Did they perceive they would always move and anticipate placements would not work out as ***** appears to?

Outcome:The reflections from after the interview, the coding and memos helped identify further question to add to the interviews. In this example, the questions added included:• What did you know about what was going to happen when you moved? How did you find this out? - and how did you respond to this? / did this effect you ? – how?• What did you expect in future placement moves? Why do you think

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you expected this?• Can you tell me what was important to you when you moved placements and why?

Appendix H: Participant Information Sheet

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Participant information sheet

(Young person 16+)

The experience and impact of foster placement breakdowns: The young person’s perspective

A research project

Please will you help with my research?

This sheet gives some information about the project to help you decide if you would like to participate in this study.

Who am I?

My name is Ruth Hunter and I am training to become a Clinical Psychologist. I am undertaking a study and would like to invite you to participate in this. This information sheet is designed to help you understand what the project is about and what would be involved in participating in this.

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What is the research?

My research is looking into collecting the views of individuals who have been in foster care and experienced placement breakdowns during this time.

Why is the research being done?

Placement breakdowns in foster care are distressing times for young people but research into how individuals would like to be supported during these times has often focussed on only asking adults around the young person their views rather than asking the young people themselves. This has led to people not knowing exactly how it feels for young people to experience a placement breakdown and the impact it has on them. We also do not know young people’s views on what could help make it better. This research aims to begin to fill in these gaps in information in order to help guide professionals to better support young people during placement breakdowns.

What will my participation involve?

I am looking to meet with individuals to ask them some questions about their last placement breakdown; what this experience was like for them and what the impact of it has been; how young people reacted and responded to this event. I would like to meet to ask you these questions but can ask these over a telephone conversation if this is easier, or over email. I will only need to do this once and it will not take more than one hour.

You will be offered a £15 iTunes voucher for participating in the study to thank you for giving up your time to meet with me.

Who will be in the project?

I am hoping to meet with individuals between 12 and 21 years of age who are or have been in foster care and experienced a placement breakdown after the age of 12.

What will happen with my information?

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I will record the interview I undertake with you to help me remember what we discussed and then transcribe this. Your information will be anonymised before I analyse what you say and when I write this up. It will be put with data from other young people to help us understand young people’s experiences. My supervisor, a transcriber and I will be the only people that see all of your data. Some of other work colleagues may see other sections of the transcribed interview, just to help check that I have collected all that I can from the information. They will only see completely anonymised parts of your interview. Your information will be treated confidentially by all of these people.

How do I take part or let you know if I do not want to?

If you would still like to take part, I would be very grateful if you could email me to inform me of this ([email protected]) and I will arrange to meet with you, call you or email you to answer any further questions you may have. If you are under 16 years I will need your Guardian’s consent for you to participate. I will ask you to sign a form that you are willing to take part in the study. If you agree to take part I will then arrange to meet with you again to ask you about your experiences. If you are interested then I can contact you again at the end of the study to inform you of what I have found from my research.

Could there be any problems for me if I take part?

Placement breakdowns can be unpleasant and / or difficult experiences. It is possible that thinking and talking about these experiences may be upsetting. If you feel upset when we are talking about them then you are welcome to stop and have a break and then continue or you can stop all together. I will give everyone written information of people and organisations that are available if you feel there are feelings or experiences you would like support in thinking more about. Your information will be treated confidentially but if you share information that you or someone else is at risk of harm then I will need to share this information with an appropriate individual, but I will discuss this with you first if I need to do this.

How will doing the research help?

When your answers are put together with all the other participants I hope it will tell us something about young people's views of foster placement breakdowns

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and how they would like support during such times. I will write a summary of these findings to help those who work with young people to understand what I have found out. Your privacy will be respected and your data will be used anonymously: No one will know that you have taken part aside from me and my supervisor (and if you are 16 or younger, your Guardian).

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Appendix I: Consent form

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Consent to participate in research: Young Person

Researcher: Ruth Hunter, Trainee Clinical Psychologist

Supervisor: Mary John, Registered Clinical Psychologist, HCPC registered

Project: What is the experience and impact of foster placement breakdowns from the perspective of the young person?

I agree to take part in this study and to be audio recorded in the interview. (If undertaking a telephone or face-to-face interview).

I agree for my data (what I say and talk about) to be used in this study and understand that my data will be treated confidentially and stored safely.

I understand that my help in this study is my choice and I have the right to withdraw from the study within two weeks of undertaking the interview. I understand that after this it will not be possible to withdraw my information.

I understand that the results of this study may be published at a later stage but information that may identify me will not be included.

I have read and understand the statements above and agree to take part in this study

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Signature:……………………………………… Date:……………………

Appendix J: Description of Analysis - Willig’s (2009) Abbreviated Grounded Theory Approach

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Coding

Coding aims to break down the data into component parts. Initial codes were given first, to identify important words or groups of words in the data. Both categories and In vivo codes were labelled using the language of the young people to aim to reduce the risk of the 'child's perspective' becoming a 'child perspective' (Soderback, Coyne & Harder, 2011).

Intermediate coding followed later (though the concurrent nature of data collection and analysis means the researcher moves between the initial and intermediate coding stages). This involved connecting sub-categories but also linking categories, exploring the range of properties and dimensions of these.

Memos

Memos are written records of the thinking of a researcher during the process of undertaking a grounded theory approach that aim to help with data comparison, guide data gathering and enable the exploration of relationships between categories. Short, explicit memos were used here as well as the exploration of more detailed memos encompassing reflections and questions for further exploration. They helped guide further exploration and data collection as well as began to synthesise the comparisons and categories into a more cohesive understanding of the data, moving towards developing a framework. An example of this memo is listed in Appendix J.

Theoretical sampling

Theoretical sampling helped give focus and direction to the constant comparative actions and analysis of the data by the researcher. It helped identify when more information is needed for categories to become saturated. The Memos were important in helping direct the decisions as to where to obtain this information.

Theoretical Saturation and Theory generation

Due to limited participants and resources, full theoretical saturation was not achieved and therefore only a developing framework was produced from the

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data. Visual diagrams were produced of the findings, highlighting the complex relationships between the concepts and categories that emerged through data analysis.

Participant validation

The findings were presented to participants to obtain their feedback and ensure that they perceived that the model represented their experiences. Following feedback, further analysis occurred and impacted the developing theory.

Credibility

Analytic credibility in Grounded Theory is improved by the emergent and interactive approach to coding leads to analysis that is influenced but not wholly determined by the researcher. Comparative analysis by the researcher aimed to help ensure the usefulness and robustness of the codes.

Theoretical Credibility is dependent on analytical credibility. In itself it is improved by the systematic use of theoretical sampling to explore and develop understanding of properties of tentative categories. Allowing participants to choose the stories they shared before focussing in on more specific lines of questioning by the researcher also helped to ensure neglect of information and a focus on specific information by the researcher (Dey, 1999). Though in this case, it was not possible to return to participants for multiple interviews, systematic follow-up of elements highlighted in previous data analysis aimed to improve theoretical credibility.

Yardley (2000) proposed four principles to help improve credibility further in the study. These included the researcher ensuring sensitivity to the context by staying close to the data and reviewing literature to (when appropriate) build theoretically upon the work of previous researchers. Supervision throughout data analysis alongside seeking guidance on the analysis process aimed to improve the competence of the researcher. Within this, supervision ensured and enhanced the transparency of the process, as well as monitored the fit of the theory with the method, key for credibility of the study. The beginnings of a coherent framework of the subject area highlight presence of the fourth key

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element from Yardley (2000) of impact and importance, important in a credible study.

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Appendix K: Example of Transcript and Coding

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Focussed Coding / Intermediate Coding

Line by Line coding / Initial coding

Transcript

Moving placements was horrible

Sister chose to leave placement without them

Bond with brother was important

Couldn’t stand being moved away from brother

Bad relationship with foster carer impacted

it was horrible my sister, she

left that family when she was sixteen to move in with her mates’ mum who fostered her

me and my brother had that bond and moving away from him was horrible.

I couldn’t stand it.

. I was depressed as soon as I moved to [town2].

]. I weren’t allowed to go to his, to go see him ‘cause I’d fell out with my foster carers

it all just happened so quick.

Too much to handle in my … in a few days

Interviewer: Ok. And when

you were going to move, kind

of, between the two

placements… How did that

go? What was it like? What

happened?

Participant: Oh, it was

horrible. It was actually

horrible because obviously …

my sister, she left that family

when she was sixteen to

move in with her mates’ mum

who fostered her and me and

my brother had that bond

and moving away from him

was horrible. Absolutely

horrible. I couldn’t stand it. I

was depressed as soon as I

moved to [town2]. I weren’t

allowed to go to his, to go see

him ‘cause I’d fell out with

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on access to see brother

Move happened too quickly too handle

Found out moving through being told they’d packed her bags

Moved on the day she found out

No warning to being moved

Placement move planning was kept a secret from her

Stuff was packed without her knowing - secrets

They didn’t. They told me they’d packed my bags.

On the day No warning they’d obviously

been planning it for a few weeks

they just didn’t tell me.

Yeah, while I was away for the weekend.

So I’d come back to find all my stuff packed and then later that day I was being moved to [town].

my foster carers. And it all

just happened so quick. Too

much to handle in my … in a

few days.

Interviewer: And how ... and

when did you find out the

placement was ending,

relative to when you were

then moved?

Participant: They didn’t.

They told me they’d packed

my bags.

Interviewer: Ok. So it was

on the day?

Participant: Mmhhmm

Interviewer: There was no

warning?

Participant: Mmmhhmm. So

they’d obviously been

planning it for a few weeks

and they just didn’t tell me.

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Moved same day found out moving - No preparation

Told by foster carer they couldn’t handle her behaviour anymore

Mixed feelings about moving

Glad to leave because of way treated

Foster carers told

They couldn’t handle my behaviour anymore.

cause I was a pretty angry child.

In a way I was glad ‘cause the way like I found they treated me

obviously unhappy as I counted them as my mum and dad.

they was there for everything, helped me like grow up and all that lot

I’m back in contact with them now. We still talk occasionally.

Interviewer: Ok. And they’d

packed your stuff… and

things?

Participant: Yeah, while I

was away for the weekend.

Interviewer: Ok.

Participant: So I’d come

back to find all my stuff

packed and then later that

day I was being moved to

[town].

Interviewer: And then what

did they say to you... was it

the foster carers that told you

or your social worker or…?

Participant: Foster carers.

They couldn’t handle my

behaviour anymore. Erm….

Yeah and all that, ‘cause I

was a pretty angry child.

Interviewer: Ok. And how

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Lost what she viewed as her mum and dad who had been helping her grow up

Now back in contact with foster carer

Not wanted at foster carer home anymore

Had to contact SS herself to sort where she was going.

SS acted immediately to find a new place

Had to sort own place from 18

obviously they didn’t want me staying there anymore

I had to get hold of my social worker and the fostering agencies to find me a new place

they done pretty much straight away.

obviously from 18 I had to sort my own place out but from going from erm, one foster family to the other, obviously social services had to be involved,

, the fostering agency had to be involved

I couldn’t say anything about it.

did you feel ….

Participant: Erm… I don’t

know really. I, like, …. In a

way I was glad ‘cause the

way like I found they treated

me but obviously unhappy as

I counted them as my mum

and dad. Like they was there

for everything, helped me like

grow up and all that lot……

I’m back in contact with them

now. We still talk

occasionally.

Interviewer: Ok. And who

moved you? (Rattling in the

background). Sorry about

that noise.

Participant: That’s alright.

Erm, well obviously they

didn’t want me staying there

anymore so obviously I had to

get hold of my social worker

and the fostering agencies to

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SS responsible for her until 18 and had no choice about this

Being moved was a secret and a surprise

Deceit – ‘behind my back’

Decisions made about her without her

No detailed explanation for move given.

So that was all done behind my back.

Next thing I know I’m moving out.

Foster carers talked about (planned) her leaving before they told her.

They didn’t even tell me really.

They just said ‘you’re going. We can’t have you no more’.

. My foster carer. Took me

They helped me unpack my stuff from the car, gave me a cuddle and then

find me a new place… which

they done pretty much

straight away.… obviously

from 18 I had to sort my own

place out but from going from

erm, one foster family to the

other, obviously social

services had to be involved,

the fostering agency had to

be involved and I couldn’t say

anything about it.

Interviewer: No?

Participant: So that was all

done behind my back. Next

thing I know I’m moving out.

Interviewer: Ok, so they’d

already joined up and talked

about it?

Participant: Mmmhhmm.

Interviewer:..by the time

the foster carers told you?

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Foster carer took to new placement

Foster carer helped her to move and then left – (practical support only)

Upset about moving

Felt had lost everything ‘all my life was gone’

All new situation at new foster carer’s

left.

It was horrible. . I was crying … felt like all my

life was gone between my feet

Moving to some house that I didn’t really know. Moving to [town], an area that I didn’t know.

Participant: Yeah.

Interviewer: Ok. Ok.

Participant: They didn’t

even tell me really. They just

said ‘you’re going. We can’t

have you no more’.

Interviewer: Ok

Participant: And then they

took me to [town2].

Interviewer: And who took

you?

Participant: My foster carer.

They helped me unpack my

stuff from the car, gave me a

cuddle and then left.

Interviewer: And how.. how

was that, having them …

Participant: It was horrible.

Absolutely horrible. I was

crying … everything. I just

felt like all my life was gone

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between my feet. Moving to

some house that I didn’t

really know. Moving to

[town], an area that I didn’t

know.

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Appendix L: Memo Examples

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Theoretical Memo: Second level – Acceptance of others’ views

Rich reports the fact that he is told he is ‘unfosterable’ without question. He reported no emotional response to being told this, no attempt to argue or disagree with social workers appearing to already believe this perspective himself. This was in contrast to his opposition in being moved to particular placements or the boundaries and instructions from foster carers, to which he reports he ‘acted out’. From the way Rich reports being told he is unfosterable it could be surmised that he was aware of this perspective long before it was verbalised to him. He report’s himself as ‘angry’ and ‘bad’ when he was in care and there appears no expectation that others should want him this way. It appears the information the social workers are sharing about the fact that he is unfosterable fits with how Rich views himself as a boy with characteristics that make him not wanted by others. There is a distinct lack of positive attributions of himself in Rich’s account, highlighting only his ability to be independent which is a strength in light of the rejection from adults in a position to offer care to him. Rich does not challenge the view of the social workers, nor does he expect them to search further to find a placement for him. There is a finality and a pervasive hopelessness of the situation that he is an unwanted child because he is naughty, something he also believes. He has no sense of entitlement to be wanted, again a mirror of the apparent attitude of the social workers in giving up on seeking a placement for him. It is unclear with whom this narrative started, whether it emerged from Rich, the social workers or others who cared for him. But it appears that there is now a cycle of this belief between Rich and his social workers.

Reflections:

In reflecting on this situation for Rich I felt a strong reaction of sadness, both in him being told such cruel information but also that this appeared to be true; that no foster parents would take him in and care for him. I found myself considering what message this must be giving Rich about his worth and his value. I feel some anger at the way this information was given by social workers; in an apparently blunt and consequently almost cruel way without clear consideration or acknowledgement of how this news may impact Rich. Consequently I was aware of feeling quite protective of Rich. His lack of emotional response struck me. I found myself considering how this apparent ‘mature response’ in accepting this piece of information could well be in contrast to the true undercurrent of feelings

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and whether the sense of hopelessness openly reported in other elements of his narrative was contributing to the lack of emotional expression spoken of here. There was a brief acknowledgement that maybe it was not appropriate for social workers to have shared this information with him in the way they did, but this was quickly followed by a focus on his maturity. I wondered whether previous descriptions of himself as ‘bad’ meant he felt he was responsible for events and could not disagree with social workers’ decisions to tell him what he perceived was the truth. And furthermore, a truth he felt responsible for.

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Appendix M: Example of a finding evidenced across interviews

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Evidence: Why the need for self-sufficiency response

- Lack of support

-could not rely on social worker

All my Social Workers have been incredibly hard to get hold of. Obviously I do appreciate that they have a huge workload but when you need someone then and now, it is important that you can get hold of them. (Sian)

They actually abused my Children’s rights. Because they made decisions without asking me… my opinion first. They did lots of things wrong. I really hated her. She was incompetent. Like she’d come along and say ‘We need to do this, this, this and this and these things’ and then wouldn’t do them herself. (Rich)

‘Cause they try and suit you with the best placement but some Social Workers don’t know their young people well enough to be able to choose that. So they end up putting them in the wrong placement and they just self-destruct. (Lisa)

I'm sure Social Workers get all the time 'I want to be moved. I don't like these people' and then it's just like one thing, like they were allowed, I don't know, a bar of chocolate or something. So I think it's, like, understandable that they were, erm, a bit 'We don't want to move them' 'cause it's a lot of hassle. But at the same time, because I'd said it so many times they never listened to me. (Sian)

I never ever thought as if they were like seriously considering it. They just said, 'We'll see how it goes in a few weeks.' And I was just at such a low point. (Adam)

Like, Ok their Social Workers supposed to…. but my Social Worker's supposed to be on my side. I didn't want it to be sides but like, they were supposed to be like helping me and erm...and I always felt as if it was like reasoning with [Foster carer] and never … it was never like what I wanted to happen. (Rich)

I felt really hurt and tricked…cheated, if you know what I mean? I thought ‘Yeah this is it. I’m gonna stay here for a while.’ But no. I felt cheated and that. (Lucy)

I think it was because it was just too much effort. It always felt like they were just like 'Oh another problem.' They probably have like so many kids to deal (Jake)

I just felt so on my own like no-one would listen to me at all. (Lisa) I would love my choice to be increased but until I hit eighteen everyone's

always trying to tell me what to do because in their eyes I'm still a child, whether I have enough maturity to take responsibility for myself or not. So whether I wanted my choice to be heard... sometimes they make decisions that were completely wrong for me, like completely wrong for who I am. Like, not what I would be happy doing but obviously they put me into a

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box; I'm a child and this is best for children so we're going to do this and it's not (Sian)

I was just so angry that my welfare… you know, like a child’s welfare comes second to money. I think that’s disgusting. Like it’s somebody’s life, it’s not just somebody’s job. Like, it might be a job to them, like having to move me and you know, paying for it, but it’s my life, rather than something that they can make decisions about, like half-heartedly. And like, they can cut corners and save money and that’s what’s important rather than my wellbeing. (Adam)

Like, it’s my wellbeing but they don’t care about that. All they cared about money. (Jake)

Because my... I met my Social … my new Social Worker on the day that I left. I didn't really know her. Like, I couldn't... Like, she was trying to comfort me because I was upset and I felt a bit... I felt a bit like she was intruding... Like, I felt like, 'This is not for you. This is something that is very private for me.' (Lucy)

I didn’t feel like I had anybody there for me, like, to talk to about it.I mean I couldn’t talk to my Social Worker; They was always busy with their other cases. (Amy)

They don't really listen to you. You're still treated as a child and like, you're not given responsibility for yourself and that you're not... you're not trusted to … to make responsible decisions for yourself. So... they kind of do what they want and put you wherever you are and you can't really control.... (Sian)

‘Cause if I had a choice I don’t think I would have gone there. But you don’t really get a choice in where you end up. That’s Social Services that. (Amy)

It's constantly criticising yourself. And like, in Social Services, the children are always being criticised. They always have to have goals to achieve. Like, they have plans to make themselves better. (Rich)

They actually told me that that’s why they were trying to move me; because they couldn’t afford it and that they thought it would be better for me to be up near lots of people I knew and my family. But it wasn’t actually at the time. (Rich)

I felt safe there and I was getting better and Social Services just pushed me and pushed me to go somewhere that I didn’t want to go. (Lisa)

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Appendix N: Example of search for triangulation of results

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Database: Psychinfo

Search terms: Foster* AND Surviv* AND Child* OR Young Pe*

OR adolescen* OR teen* OR

2005-2015. Peer-reviewed.

Results: 111

Relevant

results:

34

Key elements

highlighted in

results:

Resilience, Adversity, Thriving, trauma-related

beliefs, Self-reliance

Future, Psychodynamic adjustment (ego)

Destruction (as a means of survival)

Reactive attachment disorder,

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MRP Proposal

Impact of disrupted placements on the well-being of children who are accommodated

ByRuth Joanne Hunter

School of Psychology Faculty of Arts and Human Sciences

University of Surrey

August 2012

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Introduction

Background and theoretical rationale

In March 2011, just under 60,000 children were in foster care in the UK

(British Association of Adoption and Fostering, 2011) and three times

more likely to experience mental health difficulties than the general youth

and child population. Despite these statistics, research into interventions

and support for these fostered individuals is largely based on US

populations with limited validation of applicability to individuals in the UK.

In 1997, Berridge identified only 13 UK foster care based studies. Although

this has increased recently, understanding from studies centres only

around how to support foster carers, what effective foster care is and the

benefits of 'joined-up' service delivery in supporting foster children.

(Sellick, 2006). UK (but also international) research has frequently ignored

the experiences and views of fostered children themselves, focusing

largely on the perspectives of foster carers and other adults involved in

their care and support. This lack of information from the young people

themselves is not only unethical when determining what care they

received but also risks providing care and resources that are less effective

or at worst ineffective at meeting their needs and wishes. (DOH, 2009).

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On top of the increased risk of mental health difficulties for young people

within foster care, breakdown of placements creates further risk for

development of emotional, behavioural and mental health problems,

(Rubin et al, 2004) highlighting an important area for understanding and

appropriate support. The Children's Act (1989) highlights a duty of

professionals to facilitate contact between children in care and their

biological parents, but it is an area with on-going debates as to the costs

and benefits of this. Leathers (2003) identified that some children

experienced conflicts of loyalty between biological and foster families and

this could lead to problems of adjustment. Brown & Bednar's (2006) found

higher conflict loyalty was associated with greater emotional and

behavioural problems, difficulties that have been well-established as

positively associated with greater risk of placement breakdown. It seems

clear that the views of foster children in how they manage these

relationships is important and currently missing (Leathers, 2003), not just

in successful placements but the views of those who have experienced

placement breakdowns and are consequently at greater risk of emotional

and behavioural and mental health problems.

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In summary, we lack knowledge and understanding of how young people

themselves experience placement breakdowns in the UK and manage

their relationships with their biological families during these difficult

transitions and experiences and consequently what support they would

appreciate at this time. Understanding of resilience and needs must go

further than registering percentages of children without problems and

measuring behaviour or asking only the opinions of parents and

professionals to asking the young people themselves. (Singer et al, 2004).

If not, working in the best interests of the child, as encouraged by current

policy risks riding on incomplete information and assumptions of what

they want and need. (Sempek & Woody, 2010). This study aims to begin

to explore this area in order to build an understanding that could help

inform professionals involved in supporting young people during this time

in the most effective way.

Research Question

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What are the psychological and social impacts of disrupted placements on

the well-being of children who are accommodated?

Method

Participants

Between fifteen and twenty participants will be recruited in order to gain

enough information to produce a meaningful understanding of the topic in

question.

Inclusion Criteria

1. 21-30 years: To help ensure they are sufficiently distanced from the

experiences of disrupted placements that they are less distressed

reflecting on their experiences but recent enough to be able to

remember their experiences well.

2. Have been in foster care for at least one year*

3. One placement breakdown minimum*

4. Contact with biological parents for at least one year on entering

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foster care

5. Grew up in the UK

*. These experiences will have been occurring at or after the age of 7,

though individuals may have entered foster care earlier. The reasoning for

this age cut-off is due to children’s information processing capacity and

reliance on verbal recollection in data collection. Piaget (1983) proposed

that prior to seven years children have less organised logical thought, are

more egocentric and have fewer abstract thinking abilities which will

impact on recall of these memories. Cordon et al (2004) highlighted

experiences prior to language development will be difficult to recall

linguistically.

Exclusion criteria

Individuals who were in solely kin placements as Messing (2006)

proposed that they do not feel the trauma associated with being

removed from one's family.

Individuals with specific difficulties such as Learning Disabilities or

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developmental conditions that may make participation in the study

difficult due to potential impairments in intellectual disability and

communication.

Individuals currently seeking help from mental health services or

with a diagnosed mental health difficulty due to the possible

negative impact of the subject on them, although there is

awareness that some individuals may have mental health difficulties

that have not been formally diagnosed and / or treated.

Feasibility of recruitment

It is anticipated that adults who have experienced challenging

experiences as children will want to share their experiences for a variety

of motivations. Some may want to share their thoughts for altruistic

reasons to ensure that other young people have the benefits of services

more able to respond effectively whilst others may wish to share their

frustrations.

Recruitment Strategy

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Participants will be recruited through advertisements in the British

Association for Adoption and Fostering, local newspapers (in the Guildford

area) and advertisements on University Supervisors’ website (Ms Mary

John, Programme Director PsychD Clinical Psychology). A PhD forum that

advertises studies needing participants will also be used alongside using

the University of Surrey’s research scheme that advertises studies to

students (targeting mature students or those 21-30 years).

A brief piece of information about the study will be given and participants

will be asked to contact via email, phone or text if interested in

participating. More detailed information will then be sent and a meeting

will be arranged answer any questions and ensure the participant meets

the inclusion criteria. Following this, written consent will be discussed and

obtained if the individual wishes to participate in the study, ensuring this

is a minimum of 24 hours after receiving the detailed information sheet

about the study. If consent is given, a meeting to undertake data

collection and the interview will be arranged.

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Design and proposed data analysis

Given the lack of research in this area specifically with individuals who

have experienced placement breakdowns and disruptions, a theory of how

this is viewed and managed by individuals is lacking. Therefore this study

will be a qualitative interview study using a Grounded theory approach in

line with Charmaz (2006) in order to enable new theory to emerge in an

area that has little current understanding and no current theory specific to

this context. The focus on process and change within the Grounded

Theory approach acknowledges that what is studied is a dynamic and

socially constructed version of events and experiences which sits well in

studying the concept of 'impact' in relation to placement breakdowns.

Consequently, conclusions and findings will be acknowledged as an

interpretation of the concepts explored rather than a 'true' portrayal.

IPA is not being used as it has a narrower focus than Grounded Theory,

looking at experiences for individuals rather than enabling a wider

understanding to be developed. (Willig, 2008).

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An abbreviated version of Grounded Theory will be used due to time and

resource constraints and a likely limited number of participants. If possible

however, some initial analysis will be undertaken between interviews to

look for emerging categories to help direct further interviews more

effectively. (Willig, 2008).

It is hoped that further research may be able to explore the theory that

will be developed through this study and its application to clinical practise

to support children experiencing placement breakdowns and disruptions

in foster or adoptive care.

A narrative approach will be used in the event that few participants are

able to be recruited for the study.

Measures

Advertisements will be designed with the University of Surrey Co-

ordinator of Service User and Carer Involvement.

Information sheet. (See Appendix A*).

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Consent form*

Demographics. The following will be collected through brief

questions: current age, gender, ethnicity, age at entry to foster

care, reason for leaving biological family, number and length of

placements, number of disrupted placements / unsuccessful

placements and when these were, details of contact with biological

parents during care, presence of biological siblings in placements,

current contact with biological family

The Kinetic Family Drawing. Developed in 1970 by Burns and

Kaufman, this test requires the participant to draw a picture of his or

her entire family. This picture is meant to elicit the individuals’

attitudes toward his or her family and the overall family dynamics.

Introduction to Data collection. (See Appendix B*).

Debrief sheet. (See Appendix C*)

Audio recording equipment to record the interviews.

*These items will all be amended following consultation with service users

who have been in foster care previously but may not meet all criteria for

the study, arranged in conjunction with the Co-ordinator of Service User

and Carer involvement.

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Procedure

The participants will be interviewed alone. It will be undertaken preferably

in a room that is quiet and with limited distractions. Interviews will be

audio recorded for the purposes of transcription and in line with Grounded

Theory are likely to reduce in length as the study progresses, starting at

approximately 50 minutes. Telephone interviews will also be offered if

preferred or more convenient for the participant.

Data collection:

1. Introductions, including reminding the participants of the purpose of

the study as well as what to expect from the interview.

Confidentiality will also be discussed and the participants will be

given the opportunity to ask any questions. They will be reminded

that they can stop the interview at any time or not answer questions

that they do not wish to. This session will not be recorded to avoid

identifiable information being recorded.

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2. Demographic data will be collected through short fixed questions.

This will not be audio recorded to help protect confidentiality.

3. The Kinetic Family Drawing. Once drawn, the drawing is then

discussed with the individual to help ascertain why they have drawn

the picture in the way they have. In this scenario the drawing will be

extended to include those involved in the individual's childhood –

both biological and foster / adoptive family. Administration of this

test will also not be audio recorded to avoid recording identifiable

information but paper notes will be taken regarding the details of

the discussions. Confidentiality will be protected by the allocation of

a letter to the participant and only first names will be recorded on

the drawing. Alongside eliciting information about the individuals

view of those involved in their childhood it will provide a platform

from which to develop engagement and rapport and help the

participant feel at ease prior to undertaking the interview.

4. Semi-structured interview: In line with abbreviated Grounded

Theory, the interview will start with explorative general questions

about the research topic and the interview schedule may change as

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the participants raise topics that may appear valuable to pursue

with later participants.

This part of the study will be recorded and transcribed in adherence

to University policy for the recording, transportation and storage of

audio recordings.

5. Debrief / Ending

A debrief sheet will be given and the participant will be given the

opportunity to ask any questions they have about the study in

general or the interview and task they have just completed.

6. Follow-up

Participants will be asked if they would like to see and give feedback

on the data collected. A follow-up call will also be offered to ensure

participants' questions have been answered and they are directed

to services for further support if required.

Ethical Considerations

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Application will be made to the Faculty of Arts and Human Sciences Ethics

Committee as this study involves recruiting individuals who are potentially

vulnerable and discussion of a sensitive and potentially distressing

subject. Below is a list of potential ethical considerations in relation to this

study:

1. Discussing relationships and potentially distressing experiences of

separation and placement breakdowns from the past is a topic to be

handled sensitively and empathetically to ensure distress is

minimised. Highlighting their right to opt out of answering questions

or withdraw their consent at any time aims to help protect the

participants from feeling obliged to discuss subjects or share

information they do not wish to. Discussion prior to consent will

highlight the subject topic and support the participants in identifying

whether it is a subject they feel able to discuss without too much

distress. The debrief discussion and information sheet and follow-up

call aims to help provide a space for the participant to reduce

distress if this occurs during the interview. The interview will also

take place in a setting that is private and free from disturbances to

help reassure the participant that their privacy and feelings

discussing potentially difficult subjects are being respected.

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2. Confidentiality will be discussed in the first meeting and at the start

of the interview. If disclosures emerge through the interview, it will

be ascertained whether these have been addressed in the past and

advise of the option to discuss the matter with the police. It will also

be explored whether any other children may still be at risk and

Safeguarding procedures will be followed if appropriate.

3. Disseminating the research is important in ensuring the participants

are not subjected to discussing private and potentially distressing

issues without purpose. The research aims to help inform support of

young people experiencing placement breakdowns rather. .

Opportunities to share the findings of the research and publish the

work will therefore be sought.

4. Individuals may feel obliged to participate due to the demand

characteristics of helping others which may lead to a sense of social

compliance, an awareness of the lack of children’s voices in this

area and wanting to help other foster children be better supported.

They may not want however, to discuss such difficult topics.

Discussing the study in detail before and giving time to consent will

aim to try and combat this and ensure the participants are as

informed as possible before agreeing to do study.

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Researcher concerns

The researcher is aware of lone working policies and a risk assessment will

be undertaken with the supervisor. The University lone working policy will

be followed with the supervisor being informed of the venues and meeting

time commencement and ending.

R&D Considerations

Not required.

Service User and Carer Consultation / Involvement

Consultation will be sought from the Co-ordinator of Service User and

Carer Involvement at the University of Surrey over the design of the

adverts that will be placed on the internet and in the newspapers to

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ensure appropriate wording and explanation. Further consultation will be

sought with two service users as to the questions that will be used in the

interview to ensure they are being asked in the most appropriate,

sensitive and respectful manner. They will be amended as appropriate

following this.

Feasibility Issues

1. Difficulties in recruiting participants may arise from the reluctance

to discuss such a private and potentially distressing topic or

accessing them. Individuals may withdraw participation from the

study once the interview has started. Benefits of participating in the

study will be shared, such as helping inform professionals from the

child's perspective of how to more effectively support children

experiencing placement breakdowns in the UK will be highlighted.

2. It has been found that foster children often keep their status private

to avoid stigma and feelings of difference (Finkelstein et al, 2002)

and this may continue into adulthood and lead to a reluctance to

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express an interest in the study. For those that do express an

interest, reassurance will be given in relation to confidentiality and a

non-judgemental stance of the interview, as well as the value of

their opinions.

3. Despite the multiple methods, it may be difficult to recruit the

number of participants required. If this occurs, narrative evaluation

will be employed rather than Grounded Theory to analyse the data

collected.

4. Some individuals may find it difficult to remember some of the

demographic data required if they had numerous placements from

an early age.

5. Participants may find it difficult to talk openly about their feelings

about both their foster and biological families. Individuals may feel

loyal to those that cared for them and struggle to report more

negative aspects of their thoughts and feelings about their

experiences. Reassurance about the value of all their views and

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opinions will be given and loyalty issues will be taken into

consideration.

Dissemination strategy

Publication will be sought alongside finding other appropriate arenas such

as conferences to share the findings and help potentially inform clinical

practise and encourage further exploration of this area.

Proposed Study Timeline

Ethics Submission: 10/12

Data collection start: 01/13

complete: 08/13

Data analysis start: 08/13

complete: 10/13

Complete draft: Results / Discussion : 12/13

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Submit complete draft: 02/14

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References

Berridge, D. (1997). Foster care: A research review. London: HMSO.

British Association of Adoption and Fostering. (2011). Retrieved from: http://www.baaf.org.uk/res/stats

Brown, J., & Bednar, L. (2006). Foster parent perception of placement breakdowns. Child and. Youth Services Review, 28, 1497–1511.

Burns, R. C., & Kaufman, S. H. (1970). Kinetic family drawings (K-F-D): An introduction to understanding children through kinetic drawings. New York: Brunner/Mazel.

Charmaz, K. (2006). Constructing Grounded Theory. London: Sage.

Cordon, I. M., Pipe, M., Sayfan, L., Melinder, A., & Goodman, G. (2004). Memory for traumatic experiences in early childhood.

Developmental Review, 24, 101-132.

Department of health. (2000). Children Act 1989. London: HMSO. Retrieved from: http://www.legislation.gov.uk

Department of Health. (2009). Promoting the health and wellbeing of looked after children – revised statutory guidance. London. TSO.

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Finkelstein, M., Wamsley, M., & Miranda, D. (2002). What keeps children in foster care from succeeding in school? Views of early adolescents and the adults in their lives. Vera Institute of Justice. United States.

Leathers, S. (2003). Parental visiting, conflicting allegiances, and emotional and behavioural problems among foster children. Family relations, 52, 53-63.

Messing, J. (2006). From the Child’s Perspective: A qualitative analysis of kinship care placements. Children and Youth Services Review, 28, 1415-1434.

Piaget, J. (1983). "Piaget's Theory". In P. Mussen (Ed.) Handbook of child psychology. Wiley.

Rubin, D., Alessandrini, A., Feuddtner, C., Mandell D., Localio, R. & Hadley, T. (2004). Placement stability and mental health costs for children in foster care. Paediatrics, 113, 1336-1341.

Sellick, C. (2006). From famine to feast: A review of the foster care research literature. Children & Society, 20, 67-74.

Singer, E., Doornenbel, J. & Okma, K. (2004). Why do children resist or obey their foster parents? The inner logic of children’s behaviour

during discipline. Child Welfare league of America, 83, 581-610.

Willig, C. (2008). Introducing qualitative research in psychology. Open University Press: England.

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Literature review

UK evidence for interventions to improve the psychological wellbeing of foster children: A systematic review

Year 1

April 2012

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Abstract

Statistics from the UK highlight that foster children and young people are more than three

times more likely than those in the general youth and child population to experience mental

health difficulties. (Meltzer et al. 2003, 2004). The majority of interventions to improve foster

children's psychological wellbeing have been developed and validated in the US yet some of

these are being used in the UK. This systematic literature review looked at the research on the

effectiveness of interventions to improve the social, emotional and behavioural wellbeing of

foster children in the UK. It was a concern that few papers were found and all had substantial

methodological weaknesses that highlighted a large gap for good quality detailed research to

be undertaken to ensure professionals are appropriately and effectively supporting this

vulnerable group of individuals, directly or indirectly with the interventions they use. Future

research needs to address these methodological issues, build on current research, identify

interventions for difficulties other than behavioural problems and consider issues of diversity

and difference within this vulnerable group.

Key words: Foster, children, young people, UK, interventions, review, outcomes

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Introduction

Foster children in the UK

Statistics from Department for Education 2011 National Statistics showed that over 48,000

children were in foster care in the UK on March 31st 2011. Children and youth in foster care

have higher rates of mental health difficulties than those in the general population. Ford et al

(2007) highlighted that the results of a number of studies by Meltzer et al (2000, 2003,

2004a) emphasised that even compared to the most disadvantaged children outside the care

system, the mental health of children looked after by local authorities was significantly

worse. These studies all involved interviewing carers, teachers and children (between 11-15

years) and using the International Statistical Classification of Diseases and Health Related

Disorders (ICD-10) to identify a prevalence of a mental health disorder. This was defined by

Meltzer et al (2000) as “a clinically recognisable set of symptoms or behaviours associated

with considerable distress and substantial interference with personal functions”. Meltzer et al

(2003) found that ‘mental disorders’ were present in 40% of the fostered population in

England compared to just 13% and 10% for boys and girls between 11 and 15 years

respectively and a prevalence of 6% for children between 5-10 years in the general

population. (Meltzer et al. 2000). Meltzer et al (2004a, b) found similar prevalence rates for

foster children in Scotland and Wales. On top of this, Meltzer et al (2003) highlighted that for

looked after children in England, mental health problems (that did not reach criteria for a

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disorder) was reported for over two fifths of the children included in the study by their carers.

A study by Ward et al (2008) found that 70-80% of foster children and young people require

specialist emotional and behavioural support. Tapsfield & Collier's (2005) study reported a

37% prevalence of conduct disorder in looked-after children in the UK, which was almost

three times higher than that of the general population. Meltzer et al (2004a) identified that

after conduct disorders, emotional disorders (specifically anxiety disorders), were the most

common mental disorders in looked-after children in Scotland, England and Wales. This was

followed by hyperkinetic disorders and depression. Such increased prevalence rates highlight

the importance of effective and appropriate psychological support and interventions for foster

children.

Being healthy, staying safe, enjoying and achieving, making a positive contribution and

economic wellbeing were the five outcome aims for children proposed by the government in

2003 (Department for Education and Skills. 2003). If foster children are to be supported to

achieve the 5 outcomes then, given their increased risk and vulnerability to mental health

difficulties previously detailed then clearly a greater level of mental health support is needed

for these individuals. Best practise is to use evidenced based interventions and support when

undertaking any type of psychological support, to ensure at worst that no harm is being done,

providing the best outcome possible for the intended individuals and that the time and

resources of professionals, foster carers and foster children are not being wasted. (National

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Institute for Clinical Excellence. 2001). Cutbacks and changes in health and social services

mean that there are even fewer resources available to promote wellbeing, making it even

more essential that the interventions and psychological support being implemented are not

only the most effective, but effective for the most needy as well as those with less intense

difficulties.

Established evidence

A basic search of Ebsco, Psychinfo, Medline highlights a wealth of foster

care literature and research from the United States (US). Reviews of this

research highlight interventions and approaches to mental health care

that have the best evidence base so far. Landsverk et al's (2009) work is

the most recent published review and they reviewed the evidence for

psychosocial interventions for the most prevalent conditions found in

foster children in the US. They highlighted that for post-traumatic stress

disorder, abuse related trauma, depression, substance abuse and

disruptive behaviour disorders, interventions that addressed symptoms,

behaviour and functioning had the best (and indeed a 'strong') evidence

base. It is beyond the scope of this review to detail all the interventions

found by Landsverk et al (2009) to be promising interventions for each of

these difficulties. But they found that most interventions were brief and

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usually more effective when the caregiver was actively involved.

Interventions varied between involving multiple professionals, the child

and the carer, being community based or clinic based, and of course, the

theoretical basis for the approach, highlighting the breadth of approaches

that have been found to be effective in the US.

UK programmes being implemented

Indeed some of these US evidence-based approaches have already begun

to be implemented in the UK. McAuley & Davis (2009) identified that ten

local authorities have implemented Multi-systemic therapy (MST)

programmes for young people aged 11-17 and their families who are on

the edge of custody and an additional site piloting MST specifically for

children who have experienced abuse or neglect. MST is a US developed

intensive home-based family based intervention that acknowledges the

role of the family environment on difficulties experienced by the child and

the family. Landsverk et al (2009) identified this as an intervention with

promise, concluding from critiquing 10 studies into MFT that it was

particularly promising for working with foster children to address

substance abuse and/or disruptive behaviours. They concluded it was

positively associated with a reduction in aggressive behaviours in foster

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children and fewer placements. McAuley & Davis (2009) also identified 14

local authorities implementing Multi-dimensional Treatment Foster Care

(MTFC) programmes for adolescents aged 11-17 years, six programmes

for 3-6 year-olds and eight sites for children aged 7-11 years. McAuley &

Davis (2009) highlighted initiatives to cascade the programme out to

other local authorities. MTFC is a US established programme based on

social learning theory that aims to reduce problem behaviours and

promote developmentally appropriate and prosocial behaviour through a

multifaceted, multiple setting based approach. This includes foster

parenting in the home using specific behavioural techniques, skills

training and supportive therapy for the foster child, school consultations

and family therapy (Moore & Chamberlain. 1994). The other approach

identified as being developed when McAuley & Davis (2009) published

their research was a cognitive-behavioural programme called the

Fostering Changes Programme, which focussed on helping foster carers

manage children and was developed by Pallett et al (2002). The Fostering

Changes Programme (FCP) was the only intervention to be highlighted by

McAuley & Davis (2009) as having been developed and trialled in the UK

prior to being rolled out. It is based on 'The Incredible Years' programme

(Webster-Stratton, 1998), which was developed in the US, and aimed to

promote positive parenting and reduce children's behavioural difficulties

and improve their problem solving and social skills. The FCP trial found

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carers reported improvements in their foster children's behaviour, but

results from their other measures were less supportive of this. Through

their study, McAuley and Davis (2009) highlighted an apparent drive to

pilot interventions in the UK that had been shown to have a strong or

emerging evidence-base in the US in relation to effectiveness. They

discussed hopes that these pilots would reinforce the value of evidence-

based commissioning and gave an acknowledgement of the need to

obtain evidence of the effectiveness of these interventions for the UK

foster population. No detail however, as to how or why these interventions

may or may not be applicable in the UK was addressed in the study:

Details that seem fundamental to the predictions of whether these

interventions are likely to be effective for the UK foster population.

Services in the UK increasingly acknowledge the diversity of the UK

population itself and the impact that these differences in culture and

background may have on psychological interventions and support. Also,

foster children in themselves vary on a multitude of issues: their history,

reason for entering care, length of time in care, ethnic background,

religion, culture, etc. Identifying and acknowledging some of these

differences may provide insight into how and why the effectiveness of

interventions with an evidence-base in the US may differ in the UK and

guide appropriate adjustments or changes and the appropriateness of

implementing or testing these.

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US and UK foster care

In 2007, Thoburn published a study comparing statistics about children in out-of-home care

across a number of different countries. She noted a number of similarities and comparisons

between the US and the UK in her analysis of the statistics she collated. Thoburn (2007)

identified that a fewer percentage of those entering care were 16-17 year olds in the UK than

the US, 7% and 20% respectively and the UK had a higher percentage entering at 10-15 years

(40% to 25% respectively) but that for those under 12 months the percentages were very

similar, (17% and 15%). Thoburn's (2007) data identified that in the USA over 90% of

children were taken into out-of-home care as a result of abuse or neglect, whereas this was

only 48% for England, with other factors listed as parental disabilities or illness (8%),

disability or problems of the child (9%), abandonment (11%) and relationships or other

family problems (24%). Wales also had similar percentages to England. Thoburn (2007) also

hypothesised that using performance targets to control welfare spending was linked to seeing

out-of-home care as something to be avoided; a similarity for the USA and the UK.

Differences between the USA and the UK care system were also highlighted in the report

through comparing the legal status of children entering care on one particular day: For the

USA, over 95% entered into care as a result of a court decision, compared to only 33% in the

UK. The USA and UK had similar average lengths of time spent in out-of-home care: 1.8

year and 2.1 years respectively and both countries had a 5% adoption rate. Also, both

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countries had similar percentages of children placed in un-related foster family care: Between

47% and 57% for the four UK countries and 46% in the USA.

As highlighted earlier, Landsverk et al (2009) identified post-traumatic stress disorder, abuse

related trauma, depression, substance abuse and disruptive behaviour disorders as the most

prevalent mental health conditions of children in foster care in the US. In comparison,

Meltzer et al (2003) highlighted conduct disorders as the most common disorder experienced

by children in care (not just foster children) in the UK, followed by anxiety disorders and

hyperkinetic disorders. Statistics however do not report on the level of impact of the mental

health difficulties individually which is also likely to impact what types of support and

interventions need to be prioritised by each country.

On top of differences in legislation, characteristics and factors related to children entering

foster care; in both countries, some ethnic minorities are overrepresented in foster care. In the

UK, African Caribbean and mixed African Caribbean and white heritage are overrepresented

in foster care with black Africans overrepresented to a lesser extent. (Thoburn. 2007). In the

USA, African American and Native American children are overrepresented in out-of-home

care statistics, with Hispanic children increasingly so. (Thoburn. 2007). In the UK however,

Thoburn (2007) highlight the underrepresentation of those of East and South Asian heritage.

Statistics on the percentage of foster carers from ethnic minorities in the UK and the US are

difficult to obtain, likely due to the presence of public and private foster-care employment

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agencies and variations in data governance that create difficulties in obtaining statistics from

these. There are a range of other factors such as average number of placements, placements

with siblings, payment of foster carers and a number of other factors that may vary between

the US and the UK. These could all be issues of diversity and difference that may impact the

appropriateness or effectiveness of psychological interventions.

These statistics highlight the breadth and depth of similarities and differences between both

the foster care systems themselves and the characteristics of the children fostered in these

systems and their difficulties. As discussed, there are also likely to be many more. Given

these details, it seems complacent to assume that the evidence for effectiveness of

interventions used in the USA is automatically relevant to the UK. It highlights the

implementation of such evidence-based practises across the UK as a risky and potentially

costly trial, in terms of public money and psychosocial impact on the foster children and their

families if it is an ineffective intervention. Though US research dominates the literature

databases, one would hope that given the extent that programmes such as MST and MTFC

have already been implemented in a number of local authorities, that UK based evidence for

effectiveness is now guiding practise in the UK more than US evidence. This literature

review will now look at what evidence exists for the effectiveness of interventions for foster

children in the UK.

Method

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An electronic systematic literature search was undertaken on Psychinfo, Medline, Ebsco,

Web of Knowledge and Cochrane databases. It included peer-reviewed papers published from

January 2005 to present. The search terms used were “intervention* OR therap*”; “foster*

OR looked after OR accommodated OR” and “UK OR United Kingdom OR Brit* OR Welsh

OR Wales OR Scot* OR Northern Ireland OR Northern Irish OR Engl*”. Papers were

excluded if they did not focus on interventions and outcomes related to children while in

foster care (therefore excluding a focus on transition and adult outcomes of foster care).

Papers were also excluded if they focussed on policies rather than practise, interventions

within education rather than health, or if they focussed specifically on foster children with

additional medical health needs such as Learning Disabilities. These exclusion criteria were

used as they represent specific areas and groups that are above and beyond the scope of this

review. Papers were not excluded based on type of evidence, though consideration as to the

quality of each type of evidence is evaluated in the review in line with guidelines from the

National Institute of Clinical Excellence (NICE, 2006). Papers that discussed a theoretical

approach and used examples such as case studies were included, in order to gain an

understanding of potential areas for developments or changes to interventions.

The search was performed February 2012 and produced 11 papers that described or evaluated

interventions with foster children in the UK. These were divided into categories for

evaluation based on who was involved in the intervention; 1) foster parents 2) foster children

3) mixed focus (including combinations of foster parents, foster children, social workers,

etc.). The critique of each of the studies was focussed on the methodology, in order to

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evaluate the strength and validity of the respective results for each, in order to determine the

strength of the evidence from each paper, rather than the theoretical approach of the

intervention.

Results

Interventions with Parents of Foster Children

Interventions with foster carers are often used as indirect interventions to improve the social,

emotional and behavioural outcomes of foster children; most frequently aiming to equip

foster carers to manage foster children's difficulties, in order to improve placement stability (a

factor that can impact the social, emotional and behavioural outcomes of foster children

(Holland, Faulkner & Perez-del-Aguila. 2005)) and help foster children reach their potential.

(McDaniel et al. 2011).

Two of the papers from the search focussed on CBT based programmes for foster carers.

MacDonald et al (2005) looked at the effectiveness of CBT training for parents of foster

children with challenging behaviour. They used a randomised controlled trial (RCT) using

groups of foster carers. 117 foster carers (all but 2 of whom were white) opted into the study;

67 of these were in the training group and 50 in the control group. Data was collected before

and after the training and at 6 months follow-up. Results were that foster-carers in the

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training group reported increased confidence in ability to deal with behaviour problems and

scored higher on knowledge of behavioural principles compared to those in the control group.

McDonald et al (2005) queried whether the content and length of the course could have led to

disappointing outcomes or a lack of support to help develop the skills learnt. The authors also

suggest the limited effectiveness of the CBT training in the results could have been due to

using carers of extremely 'difficult' children. They proposed the intervention be refined to

deal with the weaknesses identified to ascertain whether in fact the intervention is ineffective

or whether this study failed to identify the effectiveness of it due to its limitations.

Herbert & Wookey (2007) investigated whether a broadly based CBT programme could

indirectly reduce the challenging behaviour of looked-after children and increase placement

stability, through improving carers' self-assurance and behaviour management skills. Their

study used a randomised controlled study, with 67 foster-carers in the experimental group and

50 in the control group. Those in the experimental group were randomly allocated into six

groups, all given the same intervention. Their ages ranged from 32 to 65 and had a mean of

8.68 years of foster experience. The intervention, the Child Wise Programme (CWP) was

devised by the authors. It is a programme that aims to be collaborative between facilitators

and foster-carers and to empower caregivers by giving them a conceptual framework (CBT

and behavioural principles and techniques) that enables them to resolve problems themselves.

Herbert & Wookey (2007) reported that CWP has obtained positive results when used with

birth parents but had not been validated for use with foster-carers, but this was not referenced

in this paper. Results were a significant increase in carers' confidence, a majority of foster

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carers reporting improvements in children's behaviour (but not to a significant level) and that

these were generally attributed to having acquired new behavioural management skills. There

was no reduction found in relation to unplanned placement breakdowns where behaviour

problems were indicated.

Though both these CBT based approaches suggest some promise in supporting foster carers

with children with challenging behaviours in the UK, both studies relied only on parent

reports of child outcomes and failed to identify detailed demographics of the foster-carers and

foster-children involved that could shed light on whom specifically these interventions may

work for. Though they used randomised controlled trials, generalisability of the results for

both studies is limited by relatively small sample sizes and drop-outs of participants, but also

for McDonald et al (2005), by the fact that carers were required to opt into the study. Also,

the study that included a six month follow-up (McDonald et al. 2005) found less positive

results of the study than Herbert & Wookey (2007), which could suggest a CBT-focussed

intervention may have limited long-term effectiveness. Unfortunately a lack of detail about

each of the programmes makes it difficult to identify the similarities and differences between

the programmes which could be helpful in investigating these approaches further.

Two other papers found looked at the effectiveness of the Incredible Years Basic Parent

(School Age) Programme (IYP) for improving foster parents ability to manage the complex

needs of looked after children by teaching them skills to manage child behaviour and

consequently promote placement stability. The IYP is founded on social learning theory and

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was originally developed for use with biological parents. It's protocol includes detailed

session plans and home activities that can be tailored by professionals to the specific needs of

families. McDaniel et al (2011) conducted a pilot programme in Northern Ireland,

implemented by Barnardo's Professional Fostering Service, using a single-group pre-test and

post-test design with 13 foster carers. McDaniel et al (2011) focussed on an age range of 8

and 13, providing some (though limited) information on this. Assessments were carried out

before and immediately after the group training and included a self-report parent rating scale

to measure the degree of conduct and externalising behaviour management problems are

exhibited by children. Results from the study suggested a significant decrease in the intensity

of social, emotional and behavioural difficulties reported by foster carers following the IYP,

and a smaller but not significant decrease in the extent to which foster carers felt their foster

child's behaviour was problematic.

Bywater et al (2008) also looked at the effectiveness of IYP. They emphasised the potential of

IYP to enhance placement stability and help foster carers understand the needs of looked-

after children. Their study focussed on 46 foster carers of children between 2 and 8 years and

employed controlled randomisation to allocate to the intervention (n=29) and control (n=17)

groups. Foster carers were approached and requested to participate in the study and received

monetary rewards for completing data at baseline and six-month follow-up. The children

ranged between 2 and 17 years at the start of the study. Results suggest that the IYP was an

effective programme for significantly reducing carer depression and reducing challenging

behaviours in the foster children, as rated by the foster carers. Bywater et al (2008)

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questioned whether their findings had been limited by using a parent-report scale that they

felt needed to be more sensitive. They also did not use other measures which reduced the

scope of measuring the changes that had occurred.

Again, despite promising findings, evidence of the effectiveness of IYP from both these

studies is limited by their small sample sizes. Bywater (2008) and McDaniel et al (2011) also

relied only on foster-carer reports to identify any impact of IYP on the foster children

themselves, and gave very limited information of the foster children and carers, limiting

understanding of who exactly the IYP appeared to be effective for. McDaniel et al (2011) also

failed to use a control group, which further limits the evidence for whether IYP is a promising

intervention. Additionally, a confounding feature in the study was Barnardo's Professional

Fostering Service provided ongoing support and training to foster carers outside of the IYP

which may have instead resulted, or contributed to the positive changes reported by the

carers. Furthermore, McDaniel et al's (2011) study failed to ascertain whether any reports of

changes or improvements from the intervention were maintained over time. A strength of

these studies was that they used quantitative measures to identify 'significant' improvements.

Though both McDaniel et al (2011) and Bywater (2009) also failed to detail many

demographics of the foster carers and foster children in their studies that could have aided

understanding of for whom the intervention was most effective (backgrounds, placements,

etc.). Overall, the study provides promising evidence but yet again another tentative start to

identifying the effectiveness of IYP for foster children.

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Gurney-Smith et al (2010) used a repeated measures design, (pre, post and three month

follow-up) design to evaluate the impact of a Fostering Attachments Group (FAG) for a

mixed group of foster and adoptive parents. FAG (Golding & Picken. 2004) is based on

social learning and attachment theories and aims to develop parenting skills by educating

about the influence of the social environment on behaviour, with consideration of the need for

responsive and attuned parenting to develop successful attachments. The group comprised of

5 foster carers and 10 adoptive parents and a special guardian; one male and 15 females.

Evaluation data was only collected from 13 participants at all three stages. Inclusion criteria

involved currently experiencing problem behaviour from a child when the group started and

difficulties in attachment relationships for that child. Referrals came from Social workers and

were active cases in the Children, Young People and Families Service. Measures used were

all parent-report tools. Analysis showed that reported parenting skills and understanding

improved to a statistically significant degree which was maintained through to follow-up. A

significant decrease in reported child hyperactivity/inattention behaviours was obtained

between pre-group and follow-up time points. Post hoc tests also found a significant decrease

in overall difficulties of the child reported between pre-group and 3 month follow-up scores.

Parenting stress levels were not impacted but children were reported to show significantly

less inhibition.

Similarly to some of the other studies, no control group was used by Gurney-Smith et al

(2010), the sample size was very small, long-term evaluation was limited (only measured at

three months after) and measures used only foster-parent reports to identify any positive

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outcomes for the foster children. The relevance of the findings to foster children is also

limited through the study using adoptive parents and a special guardian as well as foster

parents as, despite commonalities of background histories, their situations of temporary and

permanent placements may well impact the social environment quite differently. Again, as

with the other studies, though this study suggests some potential for being effective in

working with foster parents, this study fails to identify whether this approach has a truly

positive impact for the child.

Interventions directly with Foster Children

Loxterkamp (2009) aimed to challenge what she described as the ‘predominant conviction’

(p.423) that regular contact of adopted and fostered children with their biological parents is

always beneficial. Loxterkamp used three cases studies to illustrate her arguments that

contact is not always beneficial (in the short or long-term) and instead can often be the cause

of secondary harm. Though this approach highlights well the points argued by Loxterkamp

(2009) it does not provide high quality evidence that her hypotheses are valid and that the

experiences of those in her case examples are generalisable to those in the wider population.

For example, she chose the case studies to include as she felt they were representative of the

common attitudes in relation to contact. They were also chosen following therapy, as cases

Loxterkamp (2009) that had highlighted issue of biological contact that supported her

arguments, bias that cannot be ignored. Consequently, this study begins to identify potential

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issues of contact but provides poor evidence for these upon which to initiate change in a

matter that has well-established beliefs and practises associated with it.

In contrast, Sen and Broadhurst's (2011) study was a narrative review of studies into

outcomes of foster children as a result of contact with their biological family. However, they

gave little detail of the methods of the studies and detailed no quantitative outcomes. They

highlighted that evidence for the impact of biological parent contact on children's emotional,

behavioural and intellectual outcomes was largely dated and inconsistent with no studies

having employed systematic measures to evidence the effect of contact on child outcomes in

relation to both UK and International studies. The only two main papers discussed in detail in

relation to this were focussed on disruption of attachment formation through contact with

biological parents. But again, little detail of the strengths of the study or the conclusions

found were presented. Sen & Broadhurst (2011) also looked at the impact of biological parent

contact on stability of placements, but failed to link this to identifying psychosocial outcomes

for the child and again, the descriptive style provided limited insight into the strength of the

evidence found from the studies presented. Sen & Broadhurst (2011) suggest a number of

components for future research that would help improve the quality of evidence found, but

that these conclusions are valid relies on the reader assuming that these components were not

included in the studies discussed by Sen & Broadhurst (2011) based on direct omission of

these details from the review rather than detailed critique of the studies, highlighting these

omissions. Such suggestions included a need for studies using robust outcomes measures

including psychosocial profiling and children's views, sufficiently sized and representative

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samples of foster children, prospective and longitudinal designs and based on clear

definitions of contact. A lack of detail and lack of systematic approach to addressing the

literature, alongside the approach used by Loxterkamp (2009) means that evidence for the

outcomes of foster children as a result of contact with their biological parents in the UK is

currently very unclear.

The third study by Wakelyn (2008), looked at the impact of transitional therapy for children

in 'short-term' foster care. This work discussed the theories and used one case example to

illustrate the approach. It shows a promising consideration of developing and detailing new

approaches and ways of working with foster-children that take into account the importance of

well evidenced facets of practises such as multi-disciplinary working. It does not however,

provide evidence for the effectiveness of this intervention on improving the psychosocial and

behavioural outcomes of foster children given the limitations of using a case study, as with

Loxterkamp (2009).

Interventions with Multiple groups

Staines, Farmer & Selwyn (2011) investigated the effectiveness of a Therapeutic Team

Parenting approach. A prospective repeated measures design was used, involving children

between the ages of 5 and 14 entering new placements organised by one Independent Foster-

Care Agency. Twenty-three local authorities participated, 450 children were identified and

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they, their carers and social workers were sent questionnaires at the start of the placement and

one year into it. Only eighty placements had data from carers and social workers at both time

points which reduced how representative the results are of the placements as a whole. Despite

detailing some demographics of the carers, including ethnicity, age and marital status, the

sample sizes did not allow reliable detailed analysis of the result in relation to these. The team

parenting approach emphasises all team members involved with the child working

collaboratively together, assessing the young person in placement rather than in isolation. The

therapeutic fostering environment views the placement and activities provided as enabling the

fostered individual to learn and develop, based on a systemic approach. Results found high

levels of satisfaction from foster-parents for the therapeutic and team parenting approaches

and the authors concluded that high-quality placements were provided for many of the

challenging children. The authors acknowledged that the approach was not always

implemented as efficiently as intended (delays in service provision following assessment, for

example). But alongside this, due to the small return rate of questionnaires it is difficult to

determine whether this approach positively impacts placement stability or child outcomes or

whom it is particularly beneficial to. On top of this, whether this approach could be effective

outside the Independent Foster-Care sector could be questioned from debate that Independent

Foster Care Agencies often do not provide placements for the most challenging children in

the care system.

Hibbert & Frankyl (2011) also relied on qualitative analysis and were even more limited by a

small sample size in their study into the impact of a psychology consultation service set up to

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support foster carers and social workers. The approach was a consultation model that aimed

to combine clinical expertise and knowledge of psychological interventions for foster

children with the experiences and knowledge of social workers and foster carers in order is to

help foster carers understand the child’s early experience, the impact of this and then adapt

expectations of the child and strategies of working with them accordingly. Social workers

(n=7) were randomly selected but foster carers (n=7) opted into the study. They had between

1 and 6 consultation meetings (3.3 and 4.4 average for foster carers and social workers

respectively). A semi-structured interview about the consultation service was undertaken and

evaluated using thematic analysis. From this analysis, Hibbert & Frankyl (2011) highlighted

that all foster carers had reported an increase in psychological understanding of the child and

in skills for behaviour management, which in turn foster carers reported had led to improved

relationships between carers and their children and more self-confidence from this. Foster

carers also reported feeling emotionally supported. Social workers reported feeling supported

within the wider professional system, able to obtain different perspectives and reflect on

situations, gaining enhanced skills and support with decision making and planning.

Unfortunately, again no long-term investigations or child specific outcome measure were

used. Given the qualitative nature of the study and the small sample size, the generalisability

and reliability of the benefits of this approach appear are also clearly limited, though it

suggests a promising potential approach that could be worth investigating further to build on

these findings.

Golding (2010) investigated a multiagency approach to supporting children in foster care,

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using an example of an integrated multi-agency service in Worcestershire for Looked-after

and adopted children (ISL). The aim is to maximise placement stability by providing mental

health and emotional well-being guidance and advice based around a consultation process,

supported by additional facets such as network meetings, supporting parenting and providing

education and mental health interventions. The author draws upon professional clinical

experience and states that 'a range of research and audit-based evaluations has confirmed ISL

provides an effective additional level of support for the children, carers and professional

network' (p581. Golding, 2010) but does not detail what these are other than detailing that

service user views and a pilot evaluation were used. Outcomes are detailed only as foster

carers having increased confidence and a changed perception of their children following

consultation leaving a vague understanding of the added value of the team. It is also unclear

as to the value of this work for the foster children's outcomes specifically, long-term benefits

and what components of the approach may be important. Evaluations are needed to identify

this, at least to ensure it is not causing harm, if there are other benefits that motivate services

to employ such an approach.

Discussion

Overall, there is currently very little evidence for the effectiveness of any particular

intervention to improve the social, emotional and behavioural outcomes for foster children in

the UK. Firstly, interventions involving foster-carers appear to have stronger methodologies,

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using control groups and showing some attempts at identifying long-term outcomes of the

approaches used. Results from these studies all appear promising in producing positive

outcomes for carers, but unfortunately all child-related outcomes are based on parent reports

only, leading to a lack of understanding as to whether these interventions are truly have a

positive impact on foster-children. Is it enough to assume positive outcomes for a child if

their parents report being more able to cope with difficult behaviour or reduced problem

behaviours from the child? Placement stability has been evidenced as having a positive

impact on foster children’s social, emotional and behavioural outcomes, but are these studies

making assumptions that if foster parents feel more able to cope then the placement will be

more stable? Further studies need to take these questions into careful consideration.

Demographic details of foster parents and children are also limited in these studies and this

therefore limits understanding for whom these interventions may be effective and when.

Studies that have tried to consider these have been restrained by their sample sizes. Of the

foster-parent based interventions critiqued in this review, all show promise in supporting

foster carers and potentially foster children in relation to challenging behaviour particularly,

but due to methodological issues it is difficult to identify if any show more promise than

others currently. Secondly, interventions that directly involve the foster child are currently

lacking in numbers and development: Only Wakelyn (2008) has discussed a specific

approach and Loxterkamp (2009) and Sen & Broadhurst (2011) looked at the common

practise of contact with biological parents. Methods to evaluate these are also weak, with a

lack of controlled trials and use of measures to identify child outcomes. Thirdly, interventions

that include a range of individuals including carers, professionals and sometimes foster-

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children themselves seem to be even more difficult to ascertain whether they are having a

positive impact on foster children's psychosocial wellbeing: All these studies looked at failed

to use control groups and had small sample sizes or relatively high drop-out rates (or

incomplete data). Alongside this, they also relied on parent-report of child improvements and

changes, rather than multiple perspectives further highlighting difficulties ascertaining

whether these approaches truly benefit foster children. The detail of the work undertaken

within each study was also lacking, leading to limited understanding about what in the

approach may have been beneficial and why. Similarly to the parent-focussed approaches,

these studies also had limited demographic data of the foster children and carers involved and

the potential impact of issues of difference and diversity on the effectiveness of the

interventions.

Overall, the approaches that currently appear to have the most established evidence as to their

effectiveness in the UK are the foster parent focussed approaches. (McDonald et al (2005);

Herbert& Wookey (2007); McDaniel et al (2011); Bywater et al (2008); Gurney-Smith et al

(2009)). These however, have much to improve on both in the quality and detail of evidence

obtained but also in the fact that they have done more to evidence their positive outcomes for

foster carers than foster children themselves and this needs to be addressed as a priority in

future research with these approaches. What is also worth highlighting, is that these

interventions focus almost solely on issues around challenging behaviours in foster children

and though this is the current most common difficulty for foster children in the UK (Tapsfield

& Collier. 2005), other difficulties and disorders experienced by foster children need effective

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and appropriate interventions also.

Limitations

Limitations of this systematic review are that the inclusion of the search terms around

location may have overlooked some papers that have been undertaken in the UK but have not

been explicitly listed as such. Despite this, it is important to consider that professionals or

researchers interested in using UK evidence-based interventions for foster care are likely to

have time pressures that limit them from long database searches to find these. Though this

leads to a potential limitation of this review, it highlights the need to label papers in a way

that facilitates their use by those whom they are most valuable to. A similar limitation may be

the use of peer-reviewed and published articles in this review: It may be that for example, the

local authorities implementing MST as discussed by McAuley & Davis (2009) may have

evaluated the effectiveness of this intervention but not shared the findings through publishing

them, or the findings may have not reached a standard to be published. Again, if such

information has not been shared or is not able to be accessed, it limits the ability of other

local authorities and services to understand the effectiveness and limitations of these

interventions in the UK and make more informed decisions on how to best support foster

children and families.

Another limitation is the inclusion of papers that have included adoptive parents as well as

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foster parents as these may have prevented the review drawing on purely foster-related

research. (e.g., Gurney-Smith et al. 2010). Despite this drawback, given the limited wealth of

research in this area, it was felt including it would enable discussion of a more approaches

being used with foster carers in the UK. The same lack of clarity may apply from having used

papers that group looked-after children rather than focus on fostered children specifically.

(e.g., Golding. 2010) Given that in 2011, 74% of looked after children were in foster

placements suggests that this group is likely to constitute a majority of those used in studies

including all looked after children and is worth considering. (Department for Education.

2011) Studies have found however, that those in residential care are statistically likely to have

greater difficulties (Meltzer et al. 2003, 2004a, b).

Future directions

Given the limited research and weaknesses in methodology discussed in this review, there are

a number of potential directions and considerations for future research. The use of RCT's in

some of the research papers critiqued is a promising step towards providing valid and reliable

findings on the effectiveness of interventions for foster children in the UK, but greater sample

sizes and avoiding using samples where individuals have 'opted in' to the study will help

enable stronger conclusions to be drawn from findings. Given the often wide range of

individuals involved in a foster-child's care, control groups are very important in validating

the impact of an intervention and future studies should consider carefully to what extent their

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research may be compromised without a control group. Just as the diversity and difference

issues between US and UK foster children, carers and systems need to be considered, so does

the diversity of foster children and their carers in the UK. Acknowledging and investigating

how issues of diversity and difference may impact the effectiveness of interventions may be

key in help identifying what interventions are effective to use in the UK. Studies may need to

investigate specific ethnic groups, children with specific lengths of time in care or particular

histories, etc., or analyse results in more general studies to identify any potential between-

group differences. Future research looking into supporting foster children with conduct

disorders through foster-parent work needs to build on the work discussed in this review and

study more carefully the outcomes for the foster children to ensure this work is having the

positive impact on the children intended. Studies that look at longitudinal outcomes for

foster-parents and children of these programmes will also be important in understanding the

value of these interventions for the foster-care population. As emphasised earlier, with a

positive and growing focus on evaluating interventions for foster children with conduct

disorder in the UK, evaluations and developments of interventions for other difficulties

experienced by UK foster children, such as emotional and anxiety disorders must not be

neglected. (Tapsfield & Collier. 2005). Depending on the focus, future work in this area may

involve developing new approaches, making adjustments to approaches or looking at the

validity and relevance of already established approaches but all done in order to ensure

interventions used with this vulnerable group are safe and effective.

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Conclusion

From this review, it is clear that the evidence base for the effectiveness of interventions that

aim to improve the social, emotional and behavioural wellbeing for UK foster children is

limited and weak. Foster-parent focused interventions in the UK show promise in helping

foster carers feel more able to manage difficult behaviour but have done little to evidence

positive outcomes for the foster children themselves. Evidence of the effectiveness for

interventions that address the social and emotional difficulties of foster children in the UK is

lacking. Consequently, there is great scope for studies that use stronger methodologies, larger

sample studies, carefully defined samples, consider diversity implications and consider long-

term effects of interventions, whether these be validating the effectiveness of studies

developed elsewhere or developing new ones. What is clear is that with this vulnerable group

of individuals, professionals have a responsibility to support these children and young people

effectively, safely and use resources wisely to do this, to ensure we help both those with the

most need but also as many individuals as possible. In order to do this, we need a greater

understanding of what interventions can enable UK foster children to achieve the best

outcomes for their current wellbeing and future.

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References

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Ford, T., Vostanis, P., Meltzer, H. & Goodman, R. (2007). Psychiatric disorder among British children looked after by local authorities: comparison with children living in private households. British Journal of Psychiatry, 190, 319-325.

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Golding, K. (2010). Multi-agency and specialist working to meet the mental health needs of children in care and adopted. Clinical Child

Psychology and Psychiatry, 15, 573-587.

Gurney-Smith, B., Granger, C., Randle, A., & Fletcher, J. (2010). ‘In time and in tune’ – the Fostering Attachments Group: capturing sustained change in both caregiver and child. Adoption & Fostering, 34, 50–60.

Herbert, M., & Wookey, J. (2007). The Child Wise Programme: A course to enhance the self-confidence and behaviour management skills of foster carers with challenging children Adoption & Fostering Journal, 31, 27-37.

Hibbert, G., & Frankl, J. (2011). A psychology consultation service for social workers and foster carers in a child and adolescent mental

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research literature. Child Welfare , 88, 49-69.

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Loxterkamp, L. (2009), 'Contact and Truth: The Unfolding Predicament inAdoption and Fostering'. Clinical Child Psychology and Psychiatry,

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Macdonald, G., & Turner, W. (2005). An experiment in helping foster-carers manage challenging behaviour. British Journal of Social Work, 35, 1265-1282.

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McDaniel, B., Braiden, H. J., Onyekwelu, J., Murphy, M., & Regan, H. (2011). Investigating the effectiveness of the incredible years basic parenting programme for foster carers in northern Ireland. Child Care in Practice, 17, 55-67.

Meltzer, H, Gatward, R, Goodman, R and Ford, T. (2000). The mental health of children and adolescents in Great Britain: summary report. London: The Stationery Office.

Meltzer, H., Gatward, R., Corbin, T., Goodman, R., Ford, T. (2003). The mental health of young people looked after by local authorities in

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Meltzer, H., Lader, D., Corbin, T., Goodman, R. and Ford, T. (2004a). The mental health of young people looked after by local authorities in Scotland. Edinburgh: The Stationery Office.

Meltzer, H., Lader, D., Corbin, T., Goodman, R., Ford, T. (2004b). The mental health of young people looked after by local authorities in Wales. London: The Stationary Office.

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Pallett C, Scott S, Blackeby K, Yule W and Weissman R (2002) Fostering changes: a cognitive-behavioural approach to help foster carers

manage children. Adoption and fostering, 26, 39-48.

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Sen, R., & Broadhurst, K. (2011). Contact between children in out of home placements and their family and friends networks: A research review. Child & Family Social Work, 16, 298-309.

Staines, J., Farmer, E., & Selwyn, J. (2011). Implementing a therapeutic team parenting approach to fostering: The experiences of one

independent foster-care agency. British Journal of Social Work, 41, 314-332.

Tapsfield, R., & Collier, F. (2005). The cost of foster care: investing in our children's future. London: British Agencies for Adoption and

Fostering/ Fostering Network.

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Social Work Monographs.

Wakelyn, J. (2008). Transitional psychotherapy for looked-after children in 'short-term' foster care. Journal of Social Work Practice, 22, 27-36.

Ward, H., Holmes, L., Soper, J., & Olsen, R. (2008). Costs and consequences of placing children in care. London: Jessica Kingsley Publishers.

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World Health Organisation. (1992). International statistical classification of diseases and related health problems (ICD-10), 10th revision. Geneva: Author.

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Literature review

UK evidence for interventions to improve the psychological wellbeing of foster children: A systematic review

ByRuth Joanne Hunter

School of Psychology Faculty of Arts and Human Sciences

University of Surrey

April 2012

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Abstract

Statistics from the UK highlight that foster children and young people are more than three

times more likely than those in the general youth and child population to experience mental

health difficulties. (Meltzer et al. 2003, 2004). The majority of interventions to improve foster

children's psychological wellbeing have been developed and validated in the US yet some of

these are being used in the UK. This systematic literature review looked at the research on the

effectiveness of interventions to improve the social, emotional and behavioural wellbeing of

foster children in the UK. It was a concern that few papers were found and all had substantial

methodological weaknesses that highlighted a large gap for good quality detailed research to

be undertaken to ensure professionals are appropriately and effectively supporting this

vulnerable group of individuals, directly or indirectly with the interventions they use. Future

research needs to address these methodological issues, build on current research, identify

interventions for difficulties other than behavioural problems and consider issues of diversity

and difference within this vulnerable group.

Key words: Foster, children, young people, UK, interventions, review, outcomes

Introduction

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Foster children in the UK

Statistics from Department for Education 2011 National Statistics showed that over 48,000

children were in foster care in the UK on March 31st 2011. Children and youth in foster care

have higher rates of mental health difficulties than those in the general population. Ford et al

(2007) highlighted that the results of a number of studies by Meltzer et al (2000, 2003,

2004a) emphasised that even compared to the most disadvantaged children outside the care

system, the mental health of children looked after by local authorities was significantly

worse. These studies all involved interviewing carers, teachers and children (between 11-15

years) and using the International Statistical Classification of Diseases and Health Related

Disorders (ICD-10) to identify a prevalence of a mental health disorder. This was defined by

Meltzer et al (2000) as “a clinically recognisable set of symptoms or behaviours associated

with considerable distress and substantial interference with personal functions”. Meltzer et al

(2003) found that ‘mental disorders’ were present in 40% of the fostered population in

England compared to just 13% and 10% for boys and girls between 11 and 15 years

respectively and a prevalence of 6% for children between 5-10 years in the general

population. (Meltzer et al. 2000). Meltzer et al (2004a, b) found similar prevalence rates for

foster children in Scotland and Wales. On top of this, Meltzer et al (2003) highlighted that for

looked after children in England, mental health problems (that did not reach criteria for a

disorder) was reported for over two fifths of the children included in the study by their carers.

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A study by Ward et al (2008) found that 70-80% of foster children and young people require

specialist emotional and behavioural support. Tapsfield & Collier's (2005) study reported a

37% prevalence of conduct disorder in looked-after children in the UK, which was almost

three times higher than that of the general population. Meltzer et al (2004a) identified that

after conduct disorders, emotional disorders (specifically anxiety disorders), were the most

common mental disorders in looked-after children in Scotland, England and Wales. This was

followed by hyperkinetic disorders and depression. Such increased prevalence rates highlight

the importance of effective and appropriate psychological support and interventions for foster

children.

Being healthy, staying safe, enjoying and achieving, making a positive contribution and

economic wellbeing were the five outcome aims for children proposed by the government in

2003 (Department for Education and Skills. 2003). If foster children are to be supported to

achieve the 5 outcomes then, given their increased risk and vulnerability to mental health

difficulties previously detailed then clearly a greater level of mental health support is needed

for these individuals. Best practise is to use evidenced based interventions and support when

undertaking any type of psychological support, to ensure at worst that no harm is being done,

providing the best outcome possible for the intended individuals and that the time and

resources of professionals, foster carers and foster children are not being wasted. (National

Institute for Clinical Excellence. 2001). Cutbacks and changes in health and social services

mean that there are even fewer resources available to promote wellbeing, making it even

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more essential that the interventions and psychological support being implemented are not

only the most effective, but effective for the most needy as well as those with less intense

difficulties.

Established evidence

A basic search of Ebsco, Psychinfo, Medline highlights a wealth of foster care literature and

research from the United States (US). Reviews of this research highlight interventions and

approaches to mental health care that have the best evidence base so far. Landsverk et al's

(2009) work is the most recent published review and they reviewed the evidence for

psychosocial interventions for the most prevalent conditions found in foster children in the

US. They highlighted that for post-traumatic stress disorder, abuse related trauma, depression,

substance abuse and disruptive behaviour disorders, interventions that addressed symptoms,

behaviour and functioning had the best (and indeed a 'strong') evidence base. It is beyond the

scope of this review to detail all the interventions found by Landsverk et al (2009) to be

promising interventions for each of these difficulties. But they found that most interventions

were brief and usually more effective when the caregiver was actively involved. Interventions

varied between involving multiple professionals, the child and the carer, being community

based or clinic based, and of course, the theoretical basis for the approach, highlighting the

breadth of approaches that have been found to be effective in the US.

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UK programmes being implemented

Indeed some of these US evidence-based approaches have already begun

to be implemented in the UK. McAuley & Davis (2009) identified that ten

local authorities have implemented Multi-systemic therapy (MST)

programmes for young people aged 11-17 and their families who are on

the edge of custody and an additional site piloting MST specifically for

children who have experienced abuse or neglect. MST is a US developed

intensive home-based family based intervention that acknowledges the

role of the family environment on difficulties experienced by the child and

the family. Landsverk et al (2009) identified this as an intervention with

promise, concluding from critiquing 10 studies into MFT that it was

particularly promising for working with foster children to address

substance abuse and/or disruptive behaviours. They concluded it was

positively associated with a reduction in aggressive behaviours in foster

children and fewer placements. McAuley & Davis (2009) also identified 14

local authorities implementing Multi-dimensional Treatment Foster Care

(MTFC) programmes for adolescents aged 11-17 years, six programmes

for 3-6 year-olds and eight sites for children aged 7-11 years. McAuley &

Davis (2009) highlighted initiatives to cascade the programme out to

other local authorities. MTFC is a US established programme based on

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social learning theory that aims to reduce problem behaviours and

promote developmentally appropriate and prosocial behaviour through a

multifaceted, multiple setting based approach. This includes foster

parenting in the home using specific behavioural techniques, skills

training and supportive therapy for the foster child, school consultations

and family therapy (Moore & Chamberlain. 1994). The other approach

identified as being developed when McAuley & Davis (2009) published

their research was a cognitive-behavioural programme called the

Fostering Changes Programme, which focussed on helping foster carers

manage children and was developed by Pallett et al (2002). The Fostering

Changes Programme (FCP) was the only intervention to be highlighted by

McAuley & Davis (2009) as having been developed and trialled in the UK

prior to being rolled out. It is based on 'The Incredible Years' programme

(Webster-Stratton, 1998), which was developed in the US, and aimed to

promote positive parenting and reduce children's behavioural difficulties

and improve their problem solving and social skills. The FCP trial found

carers reported improvements in their foster children's behaviour, but

results from their other measures were less supportive of this. Through

their study, McAuley and Davis (2009) highlighted an apparent drive to

pilot interventions in the UK that had been shown to have a strong or

emerging evidence-base in the US in relation to effectiveness. They

discussed hopes that these pilots would reinforce the value of evidence-

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based commissioning and gave an acknowledgement of the need to

obtain evidence of the effectiveness of these interventions for the UK

foster population. No detail however, as to how or why these interventions

may or may not be applicable in the UK was addressed in the study:

Details that seem fundamental to the predictions of whether these

interventions are likely to be effective for the UK foster population.

Services in the UK increasingly acknowledge the diversity of the UK

population itself and the impact that these differences in culture and

background may have on psychological interventions and support. Also,

foster children in themselves vary on a multitude of issues: their history,

reason for entering care, length of time in care, ethnic background,

religion, culture, etc. Identifying and acknowledging some of these

differences may provide insight into how and why the effectiveness of

interventions with an evidence-base in the US may differ in the UK and

guide appropriate adjustments or changes and the appropriateness of

implementing or testing these.

US and UK foster care

In 2007, Thoburn published a study comparing statistics about children in

out-of-home care across a number of different countries. She noted a

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number of similarities and comparisons between the US and the UK in her

analysis of the statistics she collated. Thoburn (2007) identified that a

fewer percentage of those entering care were 16-17 year olds in the UK

than the US, 7% and 20% respectively and the UK had a higher

percentage entering at 10-15 years (40% to 25% respectively) but that for

those under 12 months the percentages were very similar, (17% and

15%). Thoburn's (2007) data identified that in the USA over 90% of

children were taken into out-of-home care as a result of abuse or neglect,

whereas this was only 48% for England, with other factors listed as

parental disabilities or illness (8%), disability or problems of the child

(9%), abandonment (11%) and relationships or other family problems

(24%). Wales also had similar percentages to England. Thoburn (2007)

also hypothesised that using performance targets to control welfare

spending was linked to seeing out-of-home care as something to be

avoided; a similarity for the USA and the UK. Differences between the USA

and the UK care system were also highlighted in the report through

comparing the legal status of children entering care on one particular day:

For the USA, over 95% entered into care as a result of a court decision,

compared to only 33% in the UK. The USA and UK had similar average

lengths of time spent in out-of-home care: 1.8 year and 2.1 years

respectively and both countries had a 5% adoption rate. Also, both

countries had similar percentages of children placed in un-related foster

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family care: Between 47% and 57% for the four UK countries and 46% in

the USA.

As highlighted earlier, Landsverk et al (2009) identified post-traumatic

stress disorder, abuse related trauma, depression, substance abuse and

disruptive behaviour disorders as the most prevalent mental health

conditions of children in foster care in the US. In comparison, Meltzer et al

(2003) highlighted conduct disorders as the most common disorder

experienced by children in care (not just foster children) in the UK,

followed by anxiety disorders and hyperkinetic disorders. Statistics

however do not report on the level of impact of the mental health

difficulties individually which is also likely to impact what types of support

and interventions need to be prioritised by each country.

On top of differences in legislation, characteristics and factors related to

children entering foster care; in both countries, some ethnic minorities are

overrepresented in foster care. In the UK, African Caribbean and mixed

African Caribbean and white heritage are overrepresented in foster care

with black Africans overrepresented to a lesser extent. (Thoburn. 2007). In

the USA, African American and Native American children are

overrepresented in out-of-home care statistics, with Hispanic children increasingly

so. (Thoburn. 2007). In the UK however, Thoburn (2007) highlight the underrepresentation of

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those of East and South Asian heritage.

Statistics on the percentage of foster carers from ethnic minorities in the UK and the US are

difficult to obtain, likely due to the presence of public and private foster-care employment

agencies and variations in data governance that create difficulties in obtaining statistics from

these. There are a range of other factors such as average number of placements, placements

with siblings, payment of foster carers and a number of other factors that may vary between

the US and the UK. These could all be issues of diversity and difference that may impact the

appropriateness or effectiveness of psychological interventions.

These statistics highlight the breadth and depth of similarities and differences between both

the foster care systems themselves and the characteristics of the children fostered in these

systems and their difficulties. As discussed, there are also likely to be many more. Given

these details, it seems complacent to assume that the evidence for effectiveness of

interventions used in the USA is automatically relevant to the UK. It highlights the

implementation of such evidence-based practises across the UK as a risky and potentially

costly trial, in terms of public money and psychosocial impact on the foster children and their

families if it is an ineffective intervention. Though US research dominates the literature

databases, one would hope that given the extent that programmes such as MST and MTFC

have already been implemented in a number of local authorities, that UK based evidence for

effectiveness is now guiding practise in the UK more than US evidence. This literature

review will now look at what evidence exists for the effectiveness of interventions for foster

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children in the UK.

Method

An electronic systematic literature search was undertaken on Psychinfo, Medline, Ebsco,

Web of Knowledge and Cochrane databases. It included peer-reviewed papers published from

January 2005 to present. The search terms used were “intervention* OR therap*”; “foster*

OR looked after OR accommodated OR” and “UK OR United Kingdom OR Brit* OR Welsh

OR Wales OR Scot* OR Northern Ireland OR Northern Irish OR Engl*”. Papers were

excluded if they did not focus on interventions and outcomes related to children while in

foster care (therefore excluding a focus on transition and adult outcomes of foster care).

Papers were also excluded if they focussed on policies rather than practise, interventions

within education rather than health, or if they focussed specifically on foster children with

additional medical health needs such as Learning Disabilities. These exclusion criteria were

used as they represent specific areas and groups that are above and beyond the scope of this

review. Papers were not excluded based on type of evidence, though consideration as to the

quality of each type of evidence is evaluated in the review in line with guidelines from the

National Institute of Clinical Excellence (NICE, 2006). Papers that discussed a theoretical

approach and used examples such as case studies were included, in order to gain an

understanding of potential areas for developments or changes to interventions.

The search was performed February 2012 and produced 11 papers that described or evaluated

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interventions with foster children in the UK. These were divided into categories for

evaluation based on who was involved in the intervention; 1) foster parents 2) foster children

3) mixed focus (including combinations of foster parents, foster children, social workers,

etc.). The critique of each of the studies was focussed on the methodology, in order to

evaluate the strength and validity of the respective results for each, in order to determine the

strength of the evidence from each paper, rather than the theoretical approach of the

intervention.

Results

Interventions with Parents of Foster Children

Interventions with foster carers are often used as indirect interventions to improve the social,

emotional and behavioural outcomes of foster children; most frequently aiming to equip

foster carers to manage foster children's difficulties, in order to improve placement stability (a

factor that can impact the social, emotional and behavioural outcomes of foster children

(Holland, Faulkner & Perez-del-Aguila. 2005)) and help foster children reach their potential.

(McDaniel et al. 2011).

Two of the papers from the search focussed on CBT based programmes for foster carers.

MacDonald et al (2005) looked at the effectiveness of CBT training for parents of foster

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children with challenging behaviour. They used a randomised controlled trial (RCT) using

groups of foster carers. 117 foster carers (all but 2 of whom were white) opted into the study;

67 of these were in the training group and 50 in the control group. Data was collected before

and after the training and at 6 months follow-up. Results were that foster-carers in the

training group reported increased confidence in ability to deal with behaviour problems and

scored higher on knowledge of behavioural principles compared to those in the control group.

McDonald et al (2005) queried whether the content and length of the course could have led to

disappointing outcomes or a lack of support to help develop the skills learnt. The authors also

suggest the limited effectiveness of the CBT training in the results could have been due to

using carers of extremely 'difficult' children. They proposed the intervention be refined to

deal with the weaknesses identified to ascertain whether in fact the intervention is ineffective

or whether this study failed to identify the effectiveness of it due to its limitations.

Herbert & Wookey (2007) investigated whether a broadly based CBT programme could

indirectly reduce the challenging behaviour of looked-after children and increase placement

stability, through improving carers' self-assurance and behaviour management skills. Their

study used a randomised controlled study, with 67 foster-carers in the experimental group and

50 in the control group. Those in the experimental group were randomly allocated into six

groups, all given the same intervention. Their ages ranged from 32 to 65 and had a mean of

8.68 years of foster experience. The intervention, the Child Wise Programme (CWP) was

devised by the authors. It is a programme that aims to be collaborative between facilitators

and foster-carers and to empower caregivers by giving them a conceptual framework (CBT

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and behavioural principles and techniques) that enables them to resolve problems themselves.

Herbert & Wookey (2007) reported that CWP has obtained positive results when used with

birth parents but had not been validated for use with foster-carers, but this was not referenced

in this paper. Results were a significant increase in carers' confidence, a majority of foster

carers reporting improvements in children's behaviour (but not to a significant level) and that

these were generally attributed to having acquired new behavioural management skills. There

was no reduction found in relation to unplanned placement breakdowns where behaviour

problems were indicated.

Though both these CBT based approaches suggest some promise in supporting foster carers

with children with challenging behaviours in the UK, both studies relied only on parent

reports of child outcomes and failed to identify detailed demographics of the foster-carers and

foster-children involved that could shed light on whom specifically these interventions may

work for. Though they used randomised controlled trials, generalisability of the results for

both studies is limited by relatively small sample sizes and drop-outs of participants, but also

for McDonald et al (2005), by the fact that carers were required to opt into the study. Also,

the study that included a six month follow-up (McDonald et al. 2005) found less positive

results of the study than Herbert & Wookey (2007), which could suggest a CBT-focussed

intervention may have limited long-term effectiveness. Unfortunately a lack of detail about

each of the programmes makes it difficult to identify the similarities and differences between

the programmes which could be helpful in investigating these approaches further.

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Two other papers found looked at the effectiveness of the Incredible Years Basic Parent

(School Age) Programme (IYP) for improving foster parents ability to manage the complex

needs of looked after children by teaching them skills to manage child behaviour and

consequently promote placement stability. The IYP is founded on social learning theory and

was originally developed for use with biological parents. It's protocol includes detailed

session plans and home activities that can be tailored by professionals to the specific needs of

families. McDaniel et al (2011) conducted a pilot programme in Northern Ireland,

implemented by Barnardo's Professional Fostering Service, using a single-group pre-test and

post-test design with 13 foster carers. McDaniel et al (2011) focussed on an age range of 8

and 13, providing some (though limited) information on this. Assessments were carried out

before and immediately after the group training and included a self-report parent rating scale

to measure the degree of conduct and externalising behaviour management problems are

exhibited by children. Results from the study suggested a significant decrease in the intensity

of social, emotional and behavioural difficulties reported by foster carers following the IYP,

and a smaller but not significant decrease in the extent to which foster carers felt their foster

child's behaviour was problematic.

Bywater et al (2008) also looked at the effectiveness of IYP. They emphasised the potential of

IYP to enhance placement stability and help foster carers understand the needs of looked-

after children. Their study focussed on 46 foster carers of children between 2 and 8 years and

employed controlled randomisation to allocate to the intervention (n=29) and control (n=17)

groups. Foster carers were approached and requested to participate in the study and received

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monetary rewards for completing data at baseline and six-month follow-up. The children

ranged between 2 and 17 years at the start of the study. Results suggest that the IYP was an

effective programme for significantly reducing carer depression and reducing challenging

behaviours in the foster children, as rated by the foster carers. Bywater et al (2008)

questioned whether their findings had been limited by using a parent-report scale that they

felt needed to be more sensitive. They also did not use other measures which reduced the

scope of measuring the changes that had occurred.

Again, despite promising findings, evidence of the effectiveness of IYP from both these

studies is limited by their small sample sizes. Bywater (2008) and McDaniel et al (2011) also

relied only on foster-carer reports to identify any impact of IYP on the foster children

themselves, and gave very limited information of the foster children and carers, limiting

understanding of who exactly the IYP appeared to be effective for. McDaniel et al (2011) also

failed to use a control group, which further limits the evidence for whether IYP is a promising

intervention. Additionally, a confounding feature in the study was Barnardo's Professional

Fostering Service provided ongoing support and training to foster carers outside of the IYP

which may have instead resulted, or contributed to the positive changes reported by the

carers. Furthermore, McDaniel et al's (2011) study failed to ascertain whether any reports of

changes or improvements from the intervention were maintained over time. A strength of

these studies was that they used quantitative measures to identify 'significant' improvements.

Though both McDaniel et al (2011) and Bywater (2009) also failed to detail many

demographics of the foster carers and foster children in their studies that could have aided

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understanding of for whom the intervention was most effective (backgrounds, placements,

etc.). Overall, the study provides promising evidence but yet again another tentative start to

identifying the effectiveness of IYP for foster children.

Gurney-Smith et al (2010) used a repeated measures design, (pre, post and three month

follow-up) design to evaluate the impact of a Fostering Attachments Group (FAG) for a

mixed group of foster and adoptive parents. FAG (Golding & Picken. 2004) is based on

social learning and attachment theories and aims to develop parenting skills by educating

about the influence of the social environment on behaviour, with consideration of the need for

responsive and attuned parenting to develop successful attachments. The group comprised of

5 foster carers and 10 adoptive parents and a special guardian; one male and 15 females.

Evaluation data was only collected from 13 participants at all three stages. Inclusion criteria

involved currently experiencing problem behaviour from a child when the group started and

difficulties in attachment relationships for that child. Referrals came from Social workers and

were active cases in the Children, Young People and Families Service. Measures used were

all parent-report tools. Analysis showed that reported parenting skills and understanding

improved to a statistically significant degree which was maintained through to follow-up. A

significant decrease in reported child hyperactivity/inattention behaviours was obtained

between pre-group and follow-up time points. Post hoc tests also found a significant decrease

in overall difficulties of the child reported between pre-group and 3 month follow-up scores.

Parenting stress levels were not impacted but children were reported to show significantly

less inhibition.

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Similarly to some of the other studies, no control group was used by Gurney-Smith et al

(2010), the sample size was very small, long-term evaluation was limited (only measured at

three months after) and measures used only foster-parent reports to identify any positive

outcomes for the foster children. The relevance of the findings to foster children is also

limited through the study using adoptive parents and a special guardian as well as foster

parents as, despite commonalities of background histories, their situations of temporary and

permanent placements may well impact the social environment quite differently. Again, as

with the other studies, though this study suggests some potential for being effective in

working with foster parents, this study fails to identify whether this approach has a truly

positive impact for the child.

Interventions directly with Foster Children

Loxterkamp (2009) aimed to challenge what she described as the ‘predominant conviction’

(p.423) that regular contact of adopted and fostered children with their biological parents is

always beneficial. Loxterkamp used three cases studies to illustrate her arguments that

contact is not always beneficial (in the short or long-term) and instead can often be the cause

of secondary harm. Though this approach highlights well the points argued by Loxterkamp

(2009) it does not provide high quality evidence that her hypotheses are valid and that the

experiences of those in her case examples are generalisable to those in the wider population.

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For example, she chose the case studies to include as she felt they were representative of the

common attitudes in relation to contact. They were also chosen following therapy, as cases

Loxterkamp (2009) that had highlighted issue of biological contact that supported her

arguments, bias that cannot be ignored. Consequently, this study begins to identify potential

issues of contact but provides poor evidence for these upon which to initiate change in a

matter that has well-established beliefs and practises associated with it.

In contrast, Sen and Broadhurst's (2011) study was a narrative review of studies into

outcomes of foster children as a result of contact with their biological family. However, they

gave little detail of the methods of the studies and detailed no quantitative outcomes. They

highlighted that evidence for the impact of biological parent contact on children's emotional,

behavioural and intellectual outcomes was largely dated and inconsistent with no studies

having employed systematic measures to evidence the effect of contact on child outcomes in

relation to both UK and International studies. The only two main papers discussed in detail in

relation to this were focussed on disruption of attachment formation through contact with

biological parents. But again, little detail of the strengths of the study or the conclusions

found were presented. Sen & Broadhurst (2011) also looked at the impact of biological parent

contact on stability of placements, but failed to link this to identifying psychosocial outcomes

for the child and again, the descriptive style provided limited insight into the strength of the

evidence found from the studies presented. Sen & Broadhurst (2011) suggest a number of

components for future research that would help improve the quality of evidence found, but

that these conclusions are valid relies on the reader assuming that these components were not

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included in the studies discussed by Sen & Broadhurst (2011) based on direct omission of

these details from the review rather than detailed critique of the studies, highlighting these

omissions. Such suggestions included a need for studies using robust outcomes measures

including psychosocial profiling and children's views, sufficiently sized and representative

samples of foster children, prospective and longitudinal designs and based on clear

definitions of contact. A lack of detail and lack of systematic approach to addressing the

literature, alongside the approach used by Loxterkamp (2009) means that evidence for the

outcomes of foster children as a result of contact with their biological parents in the UK is

currently very unclear.

The third study by Wakelyn (2008), looked at the impact of transitional therapy for children

in 'short-term' foster care. This work discussed the theories and used one case example to

illustrate the approach. It shows a promising consideration of developing and detailing new

approaches and ways of working with foster-children that take into account the importance of

well evidenced facets of practises such as multi-disciplinary working. It does not however,

provide evidence for the effectiveness of this intervention on improving the psychosocial and

behavioural outcomes of foster children given the limitations of using a case study, as with

Loxterkamp (2009).

Interventions with Multiple groups

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Staines, Farmer & Selwyn (2011) investigated the effectiveness of a Therapeutic Team

Parenting approach. A prospective repeated measures design was used, involving children

between the ages of 5 and 14 entering new placements organised by one Independent Foster-

Care Agency. Twenty-three local authorities participated, 450 children were identified and

they, their carers and social workers were sent questionnaires at the start of the placement and

one year into it. Only eighty placements had data from carers and social workers at both time

points which reduced how representative the results are of the placements as a whole. Despite

detailing some demographics of the carers, including ethnicity, age and marital status, the

sample sizes did not allow reliable detailed analysis of the result in relation to these. The team

parenting approach emphasises all team members involved with the child working

collaboratively together, assessing the young person in placement rather than in isolation. The

therapeutic fostering environment views the placement and activities provided as enabling the

fostered individual to learn and develop, based on a systemic approach. Results found high

levels of satisfaction from foster-parents for the therapeutic and team parenting approaches

and the authors concluded that high-quality placements were provided for many of the

challenging children. The authors acknowledged that the approach was not always

implemented as efficiently as intended (delays in service provision following assessment, for

example). But alongside this, due to the small return rate of questionnaires it is difficult to

determine whether this approach positively impacts placement stability or child outcomes or

whom it is particularly beneficial to. On top of this, whether this approach could be effective

outside the Independent Foster-Care sector could be questioned from debate that Independent

Foster Care Agencies often do not provide placements for the most challenging children in

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the care system.

Hibbert & Frankyl (2011) also relied on qualitative analysis and were even more limited by a

small sample size in their study into the impact of a psychology consultation service set up to

support foster carers and social workers. The approach was a consultation model that aimed

to combine clinical expertise and knowledge of psychological interventions for foster

children with the experiences and knowledge of social workers and foster carers in order is to

help foster carers understand the child’s early experience, the impact of this and then adapt

expectations of the child and strategies of working with them accordingly. Social workers

(n=7) were randomly selected but foster carers (n=7) opted into the study. They had between

1 and 6 consultation meetings (3.3 and 4.4 average for foster carers and social workers

respectively). A semi-structured interview about the consultation service was undertaken and

evaluated using thematic analysis. From this analysis, Hibbert & Frankyl (2011) highlighted

that all foster carers had reported an increase in psychological understanding of the child and

in skills for behaviour management, which in turn foster carers reported had led to improved

relationships between carers and their children and more self-confidence from this. Foster

carers also reported feeling emotionally supported. Social workers reported feeling supported

within the wider professional system, able to obtain different perspectives and reflect on

situations, gaining enhanced skills and support with decision making and planning.

Unfortunately, again no long-term investigations or child specific outcome measure were

used. Given the qualitative nature of the study and the small sample size, the generalisability

and reliability of the benefits of this approach appear are also clearly limited, though it

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suggests a promising potential approach that could be worth investigating further to build on

these findings.

Golding (2010) investigated a multiagency approach to supporting children in foster care,

using an example of an integrated multi-agency service in Worcestershire for Looked-after

and adopted children (ISL). The aim is to maximise placement stability by providing mental

health and emotional well-being guidance and advice based around a consultation process,

supported by additional facets such as network meetings, supporting parenting and providing

education and mental health interventions. The author draws upon professional clinical

experience and states that 'a range of research and audit-based evaluations has confirmed ISL

provides an effective additional level of support for the children, carers and professional

network' (p581. Golding, 2010) but does not detail what these are other than detailing that

service user views and a pilot evaluation were used. Outcomes are detailed only as foster

carers having increased confidence and a changed perception of their children following

consultation leaving a vague understanding of the added value of the team. It is also unclear

as to the value of this work for the foster children's outcomes specifically, long-term benefits

and what components of the approach may be important. Evaluations are needed to identify

this, at least to ensure it is not causing harm, if there are other benefits that motivate services

to employ such an approach.

Discussion

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Overall, there is currently very little evidence for the effectiveness of any particular

intervention to improve the social, emotional and behavioural outcomes for foster children in

the UK. Firstly, interventions involving foster-carers appear to have stronger methodologies,

using control groups and showing some attempts at identifying long-term outcomes of the

approaches used. Results from these studies all appear promising in producing positive

outcomes for carers, but unfortunately all child-related outcomes are based on parent reports

only, leading to a lack of understanding as to whether these interventions are truly have a

positive impact on foster-children. Is it enough to assume positive outcomes for a child if

their parents report being more able to cope with difficult behaviour or reduced problem

behaviours from the child? Placement stability has been evidenced as having a positive

impact on foster children’s social, emotional and behavioural outcomes, but are these studies

making assumptions that if foster parents feel more able to cope then the placement will be

more stable? Further studies need to take these questions into careful consideration.

Demographic details of foster parents and children are also limited in these studies and this

therefore limits understanding for whom these interventions may be effective and when.

Studies that have tried to consider these have been restrained by their sample sizes. Of the

foster-parent based interventions critiqued in this review, all show promise in supporting

foster carers and potentially foster children in relation to challenging behaviour particularly,

but due to methodological issues it is difficult to identify if any show more promise than

others currently. Secondly, interventions that directly involve the foster child are currently

lacking in numbers and development: Only Wakelyn (2008) has discussed a specific

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approach and Loxterkamp (2009) and Sen & Broadhurst (2011) looked at the common

practise of contact with biological parents. Methods to evaluate these are also weak, with a

lack of controlled trials and use of measures to identify child outcomes. Thirdly, interventions

that include a range of individuals including carers, professionals and sometimes foster-

children themselves seem to be even more difficult to ascertain whether they are having a

positive impact on foster children's psychosocial wellbeing: All these studies looked at failed

to use control groups and had small sample sizes or relatively high drop-out rates (or

incomplete data). Alongside this, they also relied on parent-report of child improvements and

changes, rather than multiple perspectives further highlighting difficulties ascertaining

whether these approaches truly benefit foster children. The detail of the work undertaken

within each study was also lacking, leading to limited understanding about what in the

approach may have been beneficial and why. Similarly to the parent-focussed approaches,

these studies also had limited demographic data of the foster children and carers involved and

the potential impact of issues of difference and diversity on the effectiveness of the

interventions.

Overall, the approaches that currently appear to have the most established evidence as to their

effectiveness in the UK are the foster parent focussed approaches. (McDonald et al (2005);

Herbert& Wookey (2007); McDaniel et al (2011); Bywater et al (2008); Gurney-Smith et al

(2009)). These however, have much to improve on both in the quality and detail of evidence

obtained but also in the fact that they have done more to evidence their positive outcomes for

foster carers than foster children themselves and this needs to be addressed as a priority in

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future research with these approaches. What is also worth highlighting, is that these

interventions focus almost solely on issues around challenging behaviours in foster children

and though this is the current most common difficulty for foster children in the UK (Tapsfield

& Collier. 2005), other difficulties and disorders experienced by foster children need effective

and appropriate interventions also.

Limitations

Limitations of this systematic review are that the inclusion of the search terms around

location may have overlooked some papers that have been undertaken in the UK but have not

been explicitly listed as such. Despite this, it is important to consider that professionals or

researchers interested in using UK evidence-based interventions for foster care are likely to

have time pressures that limit them from long database searches to find these. Though this

leads to a potential limitation of this review, it highlights the need to label papers in a way

that facilitates their use by those whom they are most valuable to. A similar limitation may be

the use of peer-reviewed and published articles in this review: It may be that for example, the

local authorities implementing MST as discussed by McAuley & Davis (2009) may have

evaluated the effectiveness of this intervention but not shared the findings through publishing

them, or the findings may have not reached a standard to be published. Again, if such

information has not been shared or is not able to be accessed, it limits the ability of other

local authorities and services to understand the effectiveness and limitations of these

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interventions in the UK and make more informed decisions on how to best support foster

children and families.

Another limitation is the inclusion of papers that have included adoptive parents as well as

foster parents as these may have prevented the review drawing on purely foster-related

research. (e.g., Gurney-Smith et al. 2010). Despite this drawback, given the limited wealth of

research in this area, it was felt including it would enable discussion of a more approaches

being used with foster carers in the UK. The same lack of clarity may apply from having used

papers that group looked-after children rather than focus on fostered children specifically.

(e.g., Golding. 2010) Given that in 2011, 74% of looked after children were in foster

placements suggests that this group is likely to constitute a majority of those used in studies

including all looked after children and is worth considering. (Department for Education.

2011) Studies have found however, that those in residential care are statistically likely to have

greater difficulties (Meltzer et al. 2003, 2004a, b).

Future directions

Given the limited research and weaknesses in methodology discussed in this review, there are

a number of potential directions and considerations for future research. The use of RCT's in

some of the research papers critiqued is a promising step towards providing valid and reliable

findings on the effectiveness of interventions for foster children in the UK, but greater sample

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sizes and avoiding using samples where individuals have 'opted in' to the study will help

enable stronger conclusions to be drawn from findings. Given the often wide range of

individuals involved in a foster-child's care, control groups are very important in validating

the impact of an intervention and future studies should consider carefully to what extent their

research may be compromised without a control group. Just as the diversity and difference

issues between US and UK foster children, carers and systems need to be considered, so does

the diversity of foster children and their carers in the UK. Acknowledging and investigating

how issues of diversity and difference may impact the effectiveness of interventions may be

key in help identifying what interventions are effective to use in the UK. Studies may need to

investigate specific ethnic groups, children with specific lengths of time in care or particular

histories, etc., or analyse results in more general studies to identify any potential between-

group differences. Future research looking into supporting foster children with conduct

disorders through foster-parent work needs to build on the work discussed in this review and

study more carefully the outcomes for the foster children to ensure this work is having the

positive impact on the children intended. Studies that look at longitudinal outcomes for

foster-parents and children of these programmes will also be important in understanding the

value of these interventions for the foster-care population. As emphasised earlier, with a

positive and growing focus on evaluating interventions for foster children with conduct

disorder in the UK, evaluations and developments of interventions for other difficulties

experienced by UK foster children, such as emotional and anxiety disorders must not be

neglected. (Tapsfield & Collier. 2005). Depending on the focus, future work in this area may

involve developing new approaches, making adjustments to approaches or looking at the

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validity and relevance of already established approaches but all done in order to ensure

interventions used with this vulnerable group are safe and effective.

Conclusion

From this review, it is clear that the evidence base for the effectiveness of interventions that

aim to improve the social, emotional and behavioural wellbeing for UK foster children is

limited and weak. Foster-parent focused interventions in the UK show promise in helping

foster carers feel more able to manage difficult behaviour but have done little to evidence

positive outcomes for the foster children themselves. Evidence of the effectiveness for

interventions that address the social and emotional difficulties of foster children in the UK is

lacking. Consequently, there is great scope for studies that use stronger methodologies, larger

sample studies, carefully defined samples, consider diversity implications and consider long-

term effects of interventions, whether these be validating the effectiveness of studies

developed elsewhere or developing new ones. What is clear is that with this vulnerable group

of individuals, professionals have a responsibility to support these children and young people

effectively, safely and use resources wisely to do this, to ensure we help both those with the

most need but also as many individuals as possible. In order to do this, we need a greater

understanding of what interventions can enable UK foster children to achieve the best

outcomes for their current wellbeing and future.

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Wakelyn, J. (2008). Transitional psychotherapy for looked-after children in 'short-term' foster care. Journal of Social Work Practice, 22, 27-36.

Ward, H., Holmes, L., Soper, J., & Olsen, R. (2008). Costs and consequences of placing children in care. London: Jessica Kingsley Publishers.

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World Health Organisation. (1992). International statistical classification of diseases and related health problems (ICD-10), 10th revision. Geneva: Author.

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Overview of Clinical Experience

Adult Mental Health

This placement was based in an Adult Community Mental Health Team. The main model of

the placement was Cognitive-Behavioural Therapy (CBT), with some DBT (Dialectical

Behavioural therapy) and Schema therapy. I used these approaches to undertake individual

work with a range of individuals with a variety of difficulties including depression, bi-polar,

personality disorders and a range of anxiety disorders including Obsessive Compulsive

Disorder (OCD), hoarding, generalised anxiety, social anxiety and post-natal depression. I

also undertook joint work with social workers and community psychiatric nurses (CPNs)

doing in-home assessments and interventions as well as joint assessments with the local

substance abuse team. I co-facilitated a CBT group for clients with depression and evaluated

this to inform service developments. The neuropsychological assessments explored queried

Learning Disabilities and brain injuries.

Older People's Mental Health

This placement was based within an Older People's Community Mental Health Team and

Older People's memory service . I undertook cognitive assessments of older adults with

suspected memory loss, to help diagnose the presence dementia, including specifying the

potential type of dementia. This developed my knowledge of dementia profiles as well as the

cognitive changes associated with older age and expanded my skills in neuropsychological

assessment tests. I co-ran a support group for individuals newly diagnosed with dementia and

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their carers and I undertook training for professionals managing behaviours that challenge in

individuals with dementia. I undertook individual therapeutic work with older adults with

depression, anxiety, bereavement difficulties, and personality disorders, often alongside

physical health conditions.

Child and Adolescent Mental Health

This placement was based in a Child and Adolescent Mental Health Service (CAMHS) where

the main approach used by my supervisor was an integrative approach. Due to the nature of

the work, there was a high emphasis on a systemic approach, with elements of CBT, narrative

and psychodynamic elements. I worked with young people and their families who were

experiencing difficulties with depression, generalised anxiety, agoraphobia, PTSD, eating

difficulties, histories of sexual assault and sexual abuse, OCD, psychosis, ASD, ADHD and

Learning Disabilities. These cases expanded my experience of assessment and managing risk,

utilising positive risk management strategies and developed my working knowledge of Child

Protection procedures. I also undertook cognitive assessments of young people with queried

learning disabilities to inform future support as well as therapeutic input. I also participated in

ASD assessments and the family therapy reflecting team.

Learning Disabilities

This placement was based in a Community Team for Adults with Learning Disabilities. It

offered variety in relation to individual work, family group and consultation to staff working

in residential homes. Part of this work included functional assessments to inform behaviour

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plans and staff training as well as CBT for depression, narrative work and complex grief

work. I worked closely with staff and families to carry out assessments with clients who were

referred to psychology for difficulties living with other residents and challenging behaviour.

Whilst on this placement, I was involved in safeguarding meetings and risk assessments,

researching specific behaviours and associated risks of these alongside issues of capacity. I

also provided consultation to staff in relation to managing safeguarding behaviours in

residential homes in the context of limited resources. During this placement I undertook

cognitive assessments for dementia with clients with Down Syndrome, as well as with a

young lady with a queried Learning Disability and ASD.

Advanced competencies

This placement was based in a Paediatric Psychology team within a large hospital. This

service offers Psychological support to children and their families and medical staff. The

predominant models of this placement were systemic, narrative, behavioural models and CBT

as assessments and therapy took into account the impact of medical conditions on all the

areas of the young people's and their families' lives. This placement expanded my

understanding of the contribution of Psychology in a predominantly medical setting.

This service exists within a very diverse community of staff and clients

and provided me the opportunity to develop my skills in working through

interpreters. There was a high level of liaison between medical staff and

different medical teams, schools, education services, social services and

community medical teams. This expanded my knowledge and skills of

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care coordinating but also developed my awareness of the roles and

functions of a wider range of child focussed services.

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Academic Assessments

Year I Assessments

PROGRAMME COMPONENT

TITLE OF ASSIGNMENT

Fundamentals of Theory and Practice in Clinical Psychology (FTPCP)

Short report of WAIS-III data and practice administration

Research –SRRP Impact on symptoms of depression of a CBT for depression group

Practice case report Cognitive behavioural therapy with a middle-aged man presenting with obsessive-compulsive disorder

Problem Based Learning – Reflective Account

'Relationship to change'

Research – Literature Review

UK evidence for interventions to improve the psychological wellbeing of foster children: A systematic review

Adult – case report Assessment, cognitive behavioural formulation and therapy with a man in his thirties presenting with severe depression and post-traumatic stress disorder

Adult – case report Cognitive behavioural therapy with a woman in her late twenties presenting with anxiety and depression.

Research – Qualitative Research Project

Trainees’ perceptions and experiences of self-disclosure in a therapeutic Setting

Research – Major Research Project Proposal

Impact of disrupted placements on the well-being of children who are accommodated

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Year II Assessments

PROGRAMME COMPONENT

TITLE OF ASSESSMENT

Research Research methods and statistics test

Professional Issues Essay How do we understand the context of mental health, mental illness and mental wellbeing when people are experiencing material poverty? What psychological frameworks do we have to offer such people?

Problem Based Learning – Reflective Account

Child protection, domestic abuse, parenting and learning disabilities and kinship care

Older People – Case Report

Neuropsychological assessment for a gentleman in his eighties experiencing some mild memory difficulties

Personal and Professional Learning Discussion Groups – Process Account

Personal and Professional Learning Discussion Groups Process Account

Child and Family– Oral Presentation of Clinical Activity

Positive risk management with a mid-teenage girl

Year III Assessments

PROGRAMME COMPONENT

ASSESSMENT TITLE

Research – MRP Portfolio

Young people’s perspectives of foster placement instability: A grounded theory approach

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Personal and Professional Learning – Final Reflective Account

On becoming a clinical psychologist: A retrospective, developmental, reflective account of the experience of training

Specialist – Case Report Integrative therapy with a young girl with chronic constipation and low self-esteem

End of Portfolio.

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