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NINDS Stroke Common Data Element (CDE) Project
Stroke Outcomes and End Points Subgroup:
Recommendations
Overview
The instruments recommended here are largely consistent with thoserecommended by the National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards 1,with some minor changes. Validation of the long harmonization battery is inprocess which may inform the need for additional instrument substitutions. Werecognize the value of consistency in measurement across studies, as inconsistentoutcomes render findings across studies more difficult to reconcile.
The presentation of two batteries allows researchers to choose cognitive outcomemeasures according to the time allowances and resources of each study, as well asthe questions being addressed. While consistency across studies is ideal, werecognize that some scientific inquiries or sample populations will require themodification of these tests batteries. For instance, while the Digit-Symbolsubstitution test (WAIS-III) is recommended as a measure of speeded sequencing,
the similar Symbol-Digit Modalities Test might be substituted in samples wherepopulations have major motor deficits (e.g., hemiparesis) as an oral version exists.
The instruments below have been selected due to extensive and favorablereliability, construct validity, and predictive utility, and/or history of use in the targetpatient population.
These recommended batteries are aimed to optimize sensitivity to executive andprocessing speed deficits, while tapping the cognitive domains of memory,language, and visual-spatial functions as well.
The Outcomes and End Points Subgroups recommended measures for Emotionaland Cognitive Status are listed below. The subsequent pages describe theseinstruments in further detail.
Short Battery (Core Instruments):
o Center for Epidemiologic Studies Depression Scale (CES-D)*
o The Montreal Cognitive Assessment (MoCA)
o Trail Making Test (A&B)
Long Battery (Supplemental Instruments):
o Digit Symbol subtest of the Wechsler Adult Intelligence Scale III
o Symbol Search subtest of the Wechsler Adult Intelligence Scale III
o Stroop Test
o Hopkins Verbal Learning Test Revised
o Rey-Osterrieth Complex Figure Copy and Delay
o Boston Naming Test (BNT) 30-item version
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Stroke Outcomes and End Points Subgroup:
Recommendations
o Information Questionnaire for Cognitive Decline in the Elderly
(IQCODE)*
o Neuropsychiatric Inventory (NPI) Questionnaire
Additional instrument (Supplemental Instrument):
o Telephone Interview for Cognitive Status (TICS)
1Hachinski V, Iadecola C, Petersen RC, Breteler MM, Nyenhuis DL, Black SE, PowersWJ, DeCarli C, Merino JG, Kalaria RN, Vinters HV, Holtzman DM, Rosenberg GA,Wallin A, Dichgans M, Marler JR, Leblanc GG. National Institute of NeurologicalDisorders and Stroke-Canadian Stroke Network vascular cognitive impairmentharmonization standards. Stroke 2006;37(9):2220-2241.
* Information about the instrument is included in a separate CRF Module and is
therefore not included in this document.
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NINDS Stroke Common Data Element (CDE) Project
Stroke Outcomes and End Points Subgroup:
Recommendations
The Montreal Cognitive Assessment (MoCA)
Core/Primary Instrument also recommended by the Stroke Presentation Subgroup
PurposeThe MoCA screens patients who present with mild cognitive complaints and normal
mini-mental state examination (MMSE) scores for mild cognitive impairment (MCI).2
While the MMSE is a ubiquitous cognitive screening instrument, its relative
insensitivity to executive dysfunction and the focal cognitive deficits3 that can often
been seen in stroke render it suboptimal for cerebrovascular populations. In fact, a
recent study4 demonstrated the underestimation of cognitive deficits by the MMSE
versus the MoCA in individuals with TIAs and stroke in a large population based
study.
OverviewThe MoCA is a screening test of cognition with favorable psychometric properties.2
It screens eight domains: Visuospatial/executive, Naming, Memory, Attention,
Language, Abstraction, Delayed recall, and Orientation.
Time
The assessment takes approximately 10 minutes.
Scoring
The total possible score is 30 points (total for each domain: Visuospatial/executive
5, Naming 3, Memory None, Attention 6, Language 3, Abstraction 2,
Delayed recall 5, Orientation 6). A normal score is greater than or equal to 26
points. The suggested cut-off score [MCI or Alzheimer's disease (AD)] is any score
less than 26. One point is added for an individual who has 12 years or fewer of
formal education; however the total possible score remains the same. Note that
additional studies of optimizing cut-points in different populations are currently
underway.
Psychometric Properties
There are strong validation studies emerging across patient populations (e.g.,
cerebrovascular, MCI/AD, Parkinsons disease).1,5,6
Other Important Notes
Available in various languages (currently 31 total).
Raters using this at admission or discharge should develop a standard methodology
and scoring instructions for use in hospital setting.
Copyright Information
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Stroke Outcomes and End Points Subgroup:
Recommendations
Universities/ Foundations/ Health Professionals/ Hospitals/Clinics/ Public Health
Institutes: MoCA may be used, reproduced, and distributed, WITH prior written
permission. The test should be made available free of charge.
Commercial Entity/ Pharma sponsored research: MoCA may be used, reproduced,
and distributed, WITH prior written permission and Licensing Agreement. The test
should be made available free of charge.
For additional information, please visit website: http://www.mocatest.org/.
References1Luis C., Keegan A, & Mullan, M (2009). Cross validation of the Montreal cognitive
assessment in community dwelling older adults residing in the southeastern US.
International Journal of Geriatric Psychiatry, 24: 197-201.
2Nasreddine ZS, Phillips NA, Bedirian V, Charbonneau S, Whitehead V, Collin I,Cummings JL, Chertkow H (2005). The Montreal Cognitive Assessment, MoCA: a
brief screening tool for mild cognitive impairment. J Am Geriatr Soc, 53(4): 695-699.
3Naugle, R., & Kawczak, K. (1989). Limitations of the Mini-Mental State Examination.
Cleveland Clinic Journal of Medicine, 56, 277-281.
4Pendlebury ST, Cuthbertson FC, Welch SJ, Mehta Z, Rothwell PM. (2010).
Underestimation of cognitive impairment by mini-mental state examination versus
the montreal cognitive assessment in patients with transient ischemic attack and
stroke: a population-based study. Stroke. 2010 Jun;41(6):1290-3. Epub 2010 Apr 8.
5Popovic, IM, Seric, V, & Demarin, V. (2007). MCI in symptomatic and asymptomatic
cerebrovascular disease. J Neurol Sci, 257, 185-193.
6Zadikoff, C., Fox, SH, Tang-Wai, DF, Thomsen, T., de Bie, RM, Wadia, P, Miyasaki, J.,
Duff-Canning, S., Lang, AE, & Marras, C. (2008). A comparison of the MMSE to the
MoCA in identifying cognitive deficits in PD. Mov Disord, 23, 297-299.
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Recommendations
Trail Making Test (A&B)
Core/Primary Instrument
PurposeThe Trail Making Test is a measure of executive ability. The Trail Making Test is one
of the most sensitive measures of cognition. For instance, it has been shown to
discriminate between those with presymptomatic Alzheimer's disease (AD) and
those who remain without dementia over time.1
Overview
The first part of this test, Trails A, requires the subject to rapidly sequence numbers
from 1 through 25, with the score being the time to complete the task. The second
part, Trails B, is a more difficult cognitive flexibility task requiring the subject to
follow a sequential pattern while shifting cognitive sets, sequencing from 1 to 13while switching between numbers and letters (i.e., 1-A-2-B, etc), with the score
being the time to complete the task. The measure of interest is Trails B. Its utility
and psychometric properties are so well accepted that it is one of the few measures
that it is used across neurologic and psychiatric clinical and research patient
populations.5
Time
The assessment takes approximately 2-4 minutes for each portion.
Scoring
Scoring of A and B are reported as the number of seconds required to complete the
task. Higher scores indicate greater impairment. Performance varies by age and
education, and thus normative standards are used to classify patient performance.3
Errors affect the patients score only in that the correction of errors is included in
the completion time for the task. If a patient has not completed both parts after
five minutes, it is unnecessary to continue the test.
Psychometric Properties
Interrater reliability has been found to be high for both A and B. 2
Other Important NotesThe TMT is ubiquitous in clinical and research practice, across patient populations.4
Copyright Information
PAR, Inc. offers the Comprehensive Trail-Making Test (CTMT), a standardized set of
five visual search and sequencing tasks. For additional information, visit:
http://www4.parinc.com/Products/
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Stroke Outcomes and End Points Subgroup:
Recommendations
SpecialtyAutomated Systems Corporation offers an online version of the TrailMaking Test. For more information, visit: http://www.trailmakingtest.com/.
References1Chen P, Ratcliff G, Belle S, al. e. Cognitive test that best discriminate between
presympomatic AD and those who remain nondemented. Neurology 2000;55:1847-
1853.
2Fals-Stewart W. An Interrater Reliability Study of the Trail Making Test (Parts A and
B). Perceptual and Motor Skills, 1992, 74: 39-42.
3Heaton, R. K., Grant, I., & Matthews, C. G. (1991). Comprehensive norms for an
expanded HalsteadReitan Battery: Demographic corrections, research findings,and clinical applications. Odessa, FL: Psychological Assessment Resources.
4Lezak, MD., Howieson, DB, & Loring, DW (2004). Orientation and Attention. In:
Neuropsychological Assessment: Fourth Edition. (pg. 372-374). Oxford University
Press, NY: NY.
5Reitan RM. (1992). Trail making test. Tucson, AZ: Reitan Neuropsychology
Laboratory.
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Stroke Outcomes and End Points Subgroup:
Recommendations
Digit Symbol subtest of the Wechsler Adult Intelligence Scale III
Supplemental Instrument
Purpose
This test has been shown to predict group membership defined by processing speed
deficits, such as brain-injured versus control samples1 and has been used as a
sensitive outcome in studies identifying predictors of longitudinal decline in elders2.
Overview
The digit-symbol subtest measures the time to recode symbol and digit items. The
test requires elements of attention, visuoperceptual processing, working memory,
and psychomotor speed.
Time
Assessment takes a few minutes to complete
Scoring
The score is the number correctly coded from 0-133 in 120 seconds.
Psychometric Properties
The test demonstrates strong reliability and validity coefficients .3
Other Important Notes
N/A
Copyright Information
Copyright belongs to Pearson Education Inc. For additional information and to order
test material, visit: http://www.pearsonassessments.com/
References1DeMonte, VE, Geffen, GM, May, CR, & MacFarland, K. (2009). Improved sensitivity
of the rapid screen of mild traumatic brain injury. J Clin Exp Neuropsychology, 6, 1-
11.
2Knopman, DS, Mosley, TH, Catellier, DJ, Coker, LH, Atherosclerosis risk incommunities study brain MRI study (2009). Fourteen-year longitudinal study of
vascular risk factors, APOE genotype, and cognition: the ARIC MRI study.
Alzheimers & Dementia: the Journal of the Alzheimers Association, 5, 207-214.
3Wechsler D. (1997). Wechsler adult intelligence scale-III. New York: Psychological
Corporation.
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Recommendations
Symbol Search subtest of the Wechsler Adult Intelligence Scale III
Supplemental Instrument
PurposeThe symbol-search subtest of the WAIS III is an indicator of processing speed and
visual perception.
Overview
The symbol-search subtest requires rapid identification of targets. Specifically, for
each item the subject must search a series of five figures to see if either of two
targets occur, and mark yes or no for each item. Recent fMRI findings have shown
greater activity in the left dorsolateral prefrontal cortices associated with slower
symbol search performance.1 This subtest and the Digit-Symbol subtest together
comprise the Processing Speed Index of the WAIS-III.
Scoring
The score is the number correct in 120 seconds from 0-60.
Time
Assessment takes approximately 3 minutes.
Psychometric Properties
The subtest has shown validity in studies of adults with various neurological
disorders.2
Other Important Notes
N/A
Copyright Information
Copyright belongs to Pearson Education Inc. For additional information and to order
test material, visit: http://www.pearsonassessments.com/
References1Sweet LH, Paskavitz JF, OConnor MJ, Browndyke JN, Wellen JW, Cohen RA (2005).
FMRI correlates of the WAIS-III Symbol Search subtest. J of Int NeuropsychologicalSociety, 11, 471-6.
2Wechsler D. (1997). Wechsler adult intelligence scale-III. New York: Psychological
Corporation.
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Recommendations
Stroop Test
Supplemental Instrument
PurposeThe Stroop test is a measure of the ability to inhibit overlearned responses in the
face of conflicting information.
Overview
The Stroop test involves three trials. First, in the WORD trial, the subject reads
words of color names (e.g., red, blue) printed in black ink. Second, in the COLOR
trial, the subject identifies colors (e.g., XXXX printed in red or blue). Finally, in the
COLOR-WORD response inhibition trial, the subject must name the color in which a
word is presented, while ignoring the printed word. Thus, incongruence between the
words color and identity (e.g., the word blue presented in red) requires inhibitionand response selection.1 In a recent study of white-matter integrity, Stroop scores
demonstrated that microstructual white matter abnormalities of frontostriatal-limbic
networks are associated with executive deficits.3
Time
Assessment takes approximately 5 minutes.
Scoring
Scoring is based on the number of correct responses within a specified time.
Psychometric Properties
In a recent study, microstructual white matter abnormalities of frontostriatal-limbic
networks were associated with Stroop performance in depressed patients. 3 A large
imaging study of community-dwelling elders found that Stroop performance was
related to number of silent lacunar infarcts, larger WMLs, and more prominent
cerebral atrophy.2
Other Important Notes
N/A
Copyright InformationMultiple versions of the Stroop test are available. To date, one version of the tests
has not been shown to be clearly superior to others.
A commonly used version is the Delis-Kaplan Executive Function System (D-KEFS)
Color-Word Interference Test (CWIT). The CWIT consists of the three traditional
Stroop trials (color naming, color name reading, interference) as well as a fourth
trial in which the subject switches back and forth between naming the dissonant ink
colors and reading the conflicting color names. The stimulus booklet and forms are
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copyrighted and included as part of the D-KEFS test kit, but can be purchased
separately from the test publisher (www.pearsonassess.com).
References1Golden & Greshwater (2002). The Stroop Color and Word Test: A Manual for Clinical
and Experimental Uses. Wood Dale, IL: Stoelting Co.
2Koga H, Takashima Y, Murakawa R, Uchino A, Yuzuriha T, Yao H. (2009). Cognitive
consequences of multiple lacunes and leukoaraiosis as vascular cognitive
impairment in community-dwelling elderly individuals. J Stroke Cerebrovasc Dis.
2009 Jan;18(1):32-7.3Murphy CF, Gunning-Dixon FM, Hoptman MJ, Lim KO, Ardekani B, Shields JK, Hrabe
J, Kanellopoulos D, Shanmugham BR, Alexopoulos GS (2007). Biological Psychiatry,61, 1007-10
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Hopkins Verbal Learning Test Revised
Supplemental Instrument
PurposeTHE HVLT-R offers a brief assessment of verbal learning and memory (recognitionand recall) for individuals 16 years and older. It is easy to administer and score andis well-tolerated even by significantly impaired individuals.1
Overview
The HVLT-R requires recall of a series of 12 words over three learning trials, free
recall after a delay, and a recognition trial.
Time
The assessment takes approximately 5-10 minutes with a 25-minute delay to
complete and 2 minutes to score.
Scoring
Raw scores are derived for Total Recall, Delayed Recall, Retention (% retained), and
a Recognition Discrimination Index
Psychometric Properties
The HVLT-R correlated most strongly with other tests of verbal memory and
relatively weakly with a test of general intelligence.4 The construct validity of the
HVLT-R has been shown relative to other standard list learning tasks, 3 and it is
sensitive to dementia.2
The HVLT-R has generally modest-to-low one-year test-retest stability for several key HVLT-R component process variables.5
Other Important Notes
N/A
Copyright Information
Copyright belongs to PAR, Inc. For additional information and to order test
materials, visit: http://www4.parinc.com/Products/
References1Brandt, J. & Benedict, R. (2001). Hopkins Verbal Learning Test-Revised: Professional
Manual. PAR: Florida.
2Hogervorst, E, Combrinck, M, Lapuerta, P et al (2002). The HVLT and screening for
dementia. Dementia and Geriatric Cognitive Disorder, 13, 13-20.
3Lacritz, LH & Cullum, CM (1998). The HVLT and CVLT: A preliminary compassion.
Archives of Clinical Neuropsychology, 13, 623-628.
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4Shapiro AM, Benedict RH, Schretlen D, Brandt J (1999). The Clinical
Neuropsychologist, 13, 348-358.
5Woods, SP (2005). Test-Retest Reliability of Component Process Variables Within
the Hopkins Verbal Learning Test-Revised. Assessment, 12, 96-100.
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Rey-Osterrieth Complex Figure Copy and Delay
Supplemental Instrument
PurposeThe Rey-Osterrieth Complex Figure (ROCF) test requires the subject to copy a
complex geometric figure, providing an index of design reproduction/graphic ability.
A recall trial then taps visual memory for the stimuli.1
Overview
The ROCF is a widely used neuropsychological test for the evaluation of visuospatial
constructional ability (Copy trial) and visual memory (Immediate Recall, Delayed
Recall, and Recognition trials). It consists of three test conditions: Copy, Immediate
Recall and Delayed Recall.2
Time
The assessment takes approximately 45 minutes, including a 30-minute delay interval (timed).
Scoring
Drawings are scored based on a 36-point scoring system. The same scoring criteria
apply to all three drawing trials. Each of the 18 scoring units is scored based on
accuracy and placement criteria. Unit scores range from two (accurately drawn,
correctly placed) to zero (inaccurately drawn, incorrectly placed, unrecognizable,
omitted).2
Psychometric Properties
The test has been extensively validated across populations and has well established
normative standards.1 Intercorrelations between the ROCF and other measures, in
samples of both normal and brain-damaged subjects, indicate convergent and
discriminant validity. It reliably discriminates among brain-damaged, psychiatric,
and normal subjects. In addition, the Recognition trial provides incremental
diagnostic power compared to using recall trials alone.2
Other Important Notes
N/A
Copyright Information
Copyright belongs to PAR, Inc. For additional information and test materials, visit:
http://www4.parinc.com/Products/
References1Lezak M, Howieson DB, Loring DW, Hannay HJ, Fischer JS (2004).
Neuropsychological Assessment. Oxford University Press.
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Recommendations
2Meyers J, Meyers K (1995). Rey Complex Figure Test and Recognition Trial:
Professional Manual. PAR: Florida.
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Controlled Oral Word Association Test (COWAT) (CFL/PRW)
Supplemental Instrument
PurposeThe COWAT detects changes in word association fluency often found in various
disorders.
Overview
This lexical fluency test requires the participant to produce as many words as
possible that start with a specified letter, within a 60 second interval. 1 Studies have
shown that deficits in verbal fluency often localize to frontal structures and
pathways, and are also associated with progressive dementias.2,4
TimeThe assessment time take approximately 4 minutes.
Scoring
Patients are given three letters, one at a time, and asked to generate a list of words
that begin with the specified letter (CFL or PRW).
Psychometric Properties
The COWAT has high interrater reliability (.99).3
Other Important Notes
Higher education level is associated with better performance on COWAT. There is
little evidence of gender differences on COWAT.
Copyright Information
Copyright belongs to PAR, Inc. as part of the Multilingual Aphasia Examination. For
test materials, go to: http://www4.parinc.com/Products/
References1Benton, A., & Hamsher, K (1989). Multilingual Aphasia Examination. Iowa City: AJA
Associates.
2Micelli, G., Caltagirone, C., Gainotti, G., et al (1981). Neuropsycholgical correlates
of localized cerebral lesions in nonaphasic brain-damaged patients. J of Clin
Neuropsychology, 3, 53-63.
3Ross TP. The reliability of cluster and switch scores for the Controlled Oral Word
Association Test. Arch Clin Neuropsychol 2003; 18: 153-64.
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4Troyer, AK, Moscovitch, M, Winocur, G et al (1998). Clustering and switching on
verbal fluency tests in Alzheimers and Parkinsons disease. J of the Intl
Neuropsychological Soc, 4, 137-143.
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Boston Naming Test (BNT) 30-item version
Supplemental Instrument
PurposeThe 30-item version of the BNT was designed to differentiate between Alzheimers
disease (AD) and normal subjects. This version is useful for repeated assessments
of a naming task, as well as in situations where administration of the complete BNT
is not practical.2
Overview
The BNT and its short forms are tasks of visual confrontation naming, sensitive to
deficits in semantic retrieval. Norms for this 30-item version were developed using
a registry including normal controls, mild cognitive impairment (MCI), and AD.1
Items have been rank ordered in terms of their ability to be named, which isthought to be correlated with their frequency.
Time
The assessment takes approximately 10 minutes.
Scoring
Patients have 20 seconds to respond to each item. Each item is scored as correct,
correct with semantic cues, or correct with phonemic cues. The total score is the
number correct spontaneously or with semantic cues.
Psychometric Properties
Interjudge and intrajudge reliability were found to be high, average of 89.1% and
97.6% respectively. Overall reliability using a matrix agreement system adjusting
for chance was 91.2%.3
Other Important Notes
Spanish versions of the BNT are available.4,5
Copyright Information
The BNT is available from the Psychological Assessment Resources (PAR), 16130
North Florida Avenue, Lutz, FL 33549. For additional information, please visit:http://www4.parinc.com/Products/
References1Jefferson, AL, Wong, S., Gracer, TS, Ozonoff, A, Green, RC, & Stern RA. (2007).
Geriatric performance on an abbreviated version of the Boston naming test. Appl
Neuropsychol, 14, 215-223.
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2Mack WJ, Freed DM, Williams BW, Henderson VW (1992). Boston Naming Test:
Shortened versions for use in Alzheimers disease. J Gerontol, 47(3): 154-158.
3Nicholas LE, Brookshire RH, MacLennan DL, Schumacher JG, Porrazzo SA (1988).The Boston Naming Test: Revised Administration and Scoring Procedures and
Normative Information for Non-Brain-Damaged Adults. Clinical Aphasiology, 18:
103-115.4Pea-Casanova, J, Quinones-Ubeda, S, Gramunt-Fombuena, N, Aguilar, M, Casas, L,
Molinuevo, JL, et al. Spanish Multicenter Normative Studies (NEURONORMA Project):
norms for Boston naming test and token test. Arch Clin Neuropsychol. 2009; 24(4):
343-354.
5Ponton, MO, Satz, P, Herrera, L, Ortiz, F, Urrutia, CP, Young, R, et al. Normative data
stratified by age and education for the Neuropsychological Screening Battery forHispanics (NeSBHIS): Initial report. Journal of the International Neuropsychological
Society. 1996; 2(2): 96-104.
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Neuropsychiatric Inventory (NPI) Questionnaire
Supplemental Instrument
Purpose
The NPI-Q is used to measure 12 categories of behavioral disturbance, in particular:
Delusions, Hallucinations, Anxiety, Depression/Dysphoria, Agitation/Aggression,
Elation/Euphoria, Disinhibition, Irritability/Lability, Apathy/Indifference, Motor
Disturbance, Nighttime Behavior Problems, and Problems with Appetite/Eating. The
questionnaire is completed by a caregiver and asks whether the patient exhibits
each of the behaviors.2
Overview
The NPI Questionnaire is a validated caregiver completed questionnaire derivedfrom the original NPI. The questionnaire taps behavioral symptoms commonly
observed post-stroke (e.g., disinhibition, apathy, irritability).1
Time
The assessment takes approximately 10 minutes.
Scoring
The administrator ranks the severity of each behavior exhibited on a scale of 1 to 3,
with 3 being the most severe. The total severity score is the sum of the severity
scores obtained for each behavioral category. Additionally, the administrator ranks
the patients level of distress from each behavior, on a scale of 1 to 5, with 5
indicating the most severe level of distress. The total distress score is the sum of
the distress scores obtained for each behavioral category.2
Psychometric Properties
Test-retest reliabilityof the NPI-Q is acceptable. The NPI-Qprovides a brief, reliable,
informant-based assessment of neuropsychiatric symptoms and associated
caregiver distress that may be suitablefor use in general clinical practice.1
Other Important Notes
N/A
Copyright Information
Copyright belongs to Jeffrey L. Cummings, MD. For additional information and test
materials, visit: http://www.mapi-trust.org/services/questionnairelicensing/ and
http://npitest.net/index.html
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References1Kaufer, DI, Cummings, JL, Ketchel, P, Smith, V, MacMillan, A, Shelley, T, Lopez, OL,
& DeKosky, ST. (2000). Validation of the NPI-Q, a brief clinical form of the
neuropsychiatric inventory. J Neuropsychiatry Clin Neurosci, 12, 233-239.
2OHara R, Mumenthaler MS, Davies H, Cassidy EL, Buffum M, Namburi S, Shakoori
R, Danielsen CE, Tsui P, Noda A, Kraemer HC, Sheikh JI (2002). Cognitive status and
behavioral problems in older hospitalized patients. Annals of General Hospital
Psychiatry, 1.
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Telephone Interview for Cognitive Status (TICS)
Supplemental Instrument
Purpose
The Telephone Interview for Cognitive Status (TICS) is a brief, standardized test of
cognitive functioning that was developed for use in situations where in-person
cognitive screening is impractical or inefficient (e.g., large-scale population
screening, epidemiological surveys, with patients who are unable to appear in
person for clinical follow-up).1 It is also helpful in the diagnosis of documenting
progressive impairment, and might also identify incident disease in research
populations.3
OverviewThe TICS is designed to be administered using the telephone, however, it also may
be administered face-to-face. The TICS is particularly useful for examining visually
impaired individuals and individuals who are unable to read or write, since it does
not require vision.
The TICS is very brief and tests many of the basic cognitive functions affected by
dementia, consisting of an 11-items, that assess a variety of cognitive domains
affected by dementing disorders, including orientation to time and place, receptive
and expressive language functions, immediate verbal memory, calculation, and
verbal abstraction. It successfully differentiates carefully diagnosed Alzheimers
disease patients from healthy spouse controls and demonstrates high test-retestreliability in these populations.2
TimeThe test usually takes less than 10 minutes to administer and score.
ScoringThe individual item scores are summed to obtain the TICS Total score, ranging from0 -41.
Psychometric PropertiesThe TICS has a high test-retest reliability and excellent sensitivity and specificity for
the detection of cognitive impairment. Among elderly populations, TICS scoresapproximate a normal distribution and are not subject to the ceiling effects thatlimit the usefulness of many mental status examinations.1
Other Important NotesThe TICS has a modified version, TIC-m, which eliminates items that are difficult toverify in epidemiological study, and also included a delayed recall procedure in anattempt to increase sensitivity.2
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Before administering the telephone interview, the examiner must speak with
someone at the same location (e.g., family member, caregiver) who will serve as a
proctor to ensure that the environment is appropriate for testing and that theexaminee is able to hear spoken language at a spoken volume. All examinee
responses are recorded verbatim.1
Copyright Information
The TICS is available from the Psychological Assessment Resources (PAR). For
additional information, please visit: http://www4.parinc.com/Products/
References1 Brandt J. (2010). Telephone Interview for Cognitive Status (TICS). PAR.
http://www4.parinc.com/Products/Product.aspx?ProductID=TICS
2 Welsh KA, Breitner JCS, Magruder-Habib KM. (1993). Detection of dementia in the
elderly using telephone screening of cognitive status. Neuropsychiatry
Neuropsychol Behav Neurol. 6:103-110.
3 Plassman BL, Newman TT, Welsh KA, Helms M, Breitner JCS. (1994). Properties of
the telephone Interview for Cognitive Status: application in epidemiological and
longitudinal studies. Neuropsychiatry Neuropsychol Behav Neurol. 7:235-241
http://www4.parinc.com/Products/http://www4.parinc.com/Products/Product.aspx?ProductID=TICShttp://www4.parinc.com/Products/http://www4.parinc.com/Products/Product.aspx?ProductID=TICS