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Additional Measures Recommended Emotional Cognitive Status

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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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    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.

    Stroke Version 1.0

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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

    Stroke Version 1.0

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    NINDS Stroke Common Data Element (CDE) Project

    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.

    Stroke Version 1.0

    http://www.mocatest.org/http://www.mocatest.org/
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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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    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.

    Stroke Version 1.0

    http://www.trailmakingtest.com/http://www.trailmakingtest.com/
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    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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    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.

    Stroke Version 1.0

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    Stroke Outcomes and End Points Subgroup:

    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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    Recommendations

    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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    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

    Stroke Version 1.0

    http://www.mapi-trust.org/services/questionnairelicensing/%20%20%20http://npitest.net/index.htmlhttp://www.mapi-trust.org/services/questionnairelicensing/%20%20%20http://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

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