A recommended scale for cognitive screening in clinical trials of Parkinson's disease
Identifieur interne : 001E79 ( Main/Exploration ); précédent : 001E78; suivant : 001E80A recommended scale for cognitive screening in clinical trials of Parkinson's disease
Auteurs : Kelvin L. Chou [États-Unis] ; Melissa M. Amick [États-Unis] ; Jason Brandt [États-Unis] ; Richard Camicioli [Canada] ; Karen Frei [États-Unis] ; Darren Gitelman [États-Unis] ; Jennifer Goldman [États-Unis] ; John Growdon [États-Unis] ; Howard I. Hurtig [États-Unis] ; Bonnie Levin [États-Unis] ; Irene Litvan [États-Unis] ; Laura Marsh [États-Unis] ; Tanya Simuni [États-Unis] ; Alexander I. Tröster [États-Unis] ; Ergun Y. Uc [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2010-11-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Clinical Trials as Topic, Clinical trial, Cognition, Cognition Disorders (complications), Cognition Disorders (diagnosis), Cognition Disorders (psychology), Cognitive disorder, Humans, Medical screening, Nervous system diseases, Neuropsychological Tests, Parkinson Disease (complications), Parkinson Disease (psychology), Parkinson disease, Parkinson's disease, Psychometrics, Questionnaires, cognitive impairment, cognitive screening.
- MESH :
- complications : Cognition Disorders, Parkinson Disease.
- diagnosis : Cognition Disorders.
- psychology : Cognition Disorders, Parkinson Disease.
- Clinical Trials as Topic, Cognition, Humans, Neuropsychological Tests, Psychometrics, Questionnaires.
Abstract
Cognitive impairment is common in Parkinson's disease (PD). There is a critical need for a brief, standard cognitive screening measure for use in PD trials whose primary focus is not on cognition. The Parkinson Study Group (PSG) Cognitive/Psychiatric Working Group formed a Task Force to make recommendations for a cognitive scale that could screen for dementia and mild cognitive impairment in clinical trials of PD where cognition is not the primary outcome. This Task Force conducted a systematic literature search for cognitive assessments previously used in a PD population. Scales were then evaluated for their appropriateness to screen for cognitive deficits in clinical trials, including brief administration time (<15 minutes), assessment of the major cognitive domains, and potential to detect subtle cognitive impairment in PD. Five scales of global cognition met the predetermined screening criteria and were considered for review. Based on the Task Force's evaluation criteria the Montreal Cognitive Assessment (MoCA), appeared to be the most suitable measure. This Task Force recommends consideration of the MoCA as a minimum cognitive screening measure in clinical trials of PD where cognitive performance is not the primary outcome measure. The MoCA still requires further study of its diagnostic utility in PD populations but appears to be the most appropriate measure among the currently available brief cognitive assessments. Widespread adoption of a single instrument such as the MoCA in clinical trials can improve comparability between research studies on PD. © 2010 Movement Disorder Society
Url:
- https://api.istex.fr/document/40D88EA675753E232188B486DDBDA998C7C06B26/fulltext/pdf
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978783
DOI: 10.1002/mds.23362
Affiliations:
- Canada, États-Unis
- Californie, Caroline du Nord, Floride, Illinois, Iowa, Kentucky, Maryland, Massachusetts, Michigan, Pennsylvanie, Texas
- Iowa City
- Université de l'Iowa
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Le document en format XML
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<term>Cognition</term>
<term>Cognition Disorders (complications)</term>
<term>Cognition Disorders (diagnosis)</term>
<term>Cognition Disorders (psychology)</term>
<term>Cognitive disorder</term>
<term>Humans</term>
<term>Medical screening</term>
<term>Nervous system diseases</term>
<term>Neuropsychological Tests</term>
<term>Parkinson Disease (complications)</term>
<term>Parkinson Disease (psychology)</term>
<term>Parkinson disease</term>
<term>Parkinson's disease</term>
<term>Psychometrics</term>
<term>Questionnaires</term>
<term>cognitive impairment</term>
<term>cognitive screening</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Cognition Disorders</term>
<term>Parkinson Disease</term>
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<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cognition Disorders</term>
</keywords>
<keywords scheme="MESH" qualifier="psychology" xml:lang="en"><term>Cognition Disorders</term>
<term>Parkinson Disease</term>
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<keywords scheme="MESH" xml:lang="en"><term>Clinical Trials as Topic</term>
<term>Cognition</term>
<term>Humans</term>
<term>Neuropsychological Tests</term>
<term>Psychometrics</term>
<term>Questionnaires</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Dépistage</term>
<term>Essai clinique</term>
<term>Maladie de Parkinson</term>
<term>Pathologie du système nerveux</term>
<term>Trouble cognitif</term>
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<front><div type="abstract" xml:lang="en">Cognitive impairment is common in Parkinson's disease (PD). There is a critical need for a brief, standard cognitive screening measure for use in PD trials whose primary focus is not on cognition. The Parkinson Study Group (PSG) Cognitive/Psychiatric Working Group formed a Task Force to make recommendations for a cognitive scale that could screen for dementia and mild cognitive impairment in clinical trials of PD where cognition is not the primary outcome. This Task Force conducted a systematic literature search for cognitive assessments previously used in a PD population. Scales were then evaluated for their appropriateness to screen for cognitive deficits in clinical trials, including brief administration time (<15 minutes), assessment of the major cognitive domains, and potential to detect subtle cognitive impairment in PD. Five scales of global cognition met the predetermined screening criteria and were considered for review. Based on the Task Force's evaluation criteria the Montreal Cognitive Assessment (MoCA), appeared to be the most suitable measure. This Task Force recommends consideration of the MoCA as a minimum cognitive screening measure in clinical trials of PD where cognitive performance is not the primary outcome measure. The MoCA still requires further study of its diagnostic utility in PD populations but appears to be the most appropriate measure among the currently available brief cognitive assessments. Widespread adoption of a single instrument such as the MoCA in clinical trials can improve comparability between research studies on PD. © 2010 Movement Disorder Society</div>
</front>
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<country name="Canada"><noRegion><name sortKey="Camicioli, Richard" sort="Camicioli, Richard" uniqKey="Camicioli R" first="Richard" last="Camicioli">Richard Camicioli</name>
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