La maladie de Parkinson au Canada (serveur d'exploration)

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A Recommended Scale for Cognitive Screening in Clinical Trials of Parkinson's Disease

Identifieur interne : 000376 ( PascalFrancis/Corpus ); précédent : 000375; suivant : 000377

A Recommended Scale for Cognitive Screening in Clinical Trials of Parkinson's Disease

Auteurs : Kelvin L. Chou ; Melissa M. Amick ; Jason Brandt ; Richard Camicioli ; Karen Frei ; Darren Gitelman ; Jennifer Goldman ; John Growdon ; Howard I. Hurtig ; Bonnie Levin ; Irene Litvan ; Laura Marsh ; Tanya Simuni ; Alexander I. Tröster ; Ergun Y. Uc

Source :

RBID : Pascal:10-0512923

Descripteurs français

English descriptors

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.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A01 01  1    @0 0885-3185
A03   1    @0 Mov. disord.
A05       @2 25
A06       @2 15
A08 01  1  ENG  @1 A Recommended Scale for Cognitive Screening in Clinical Trials of Parkinson's Disease
A11 01  1    @1 CHOU (Kelvin L.)
A11 02  1    @1 AMICK (Melissa M.)
A11 03  1    @1 BRANDT (Jason)
A11 04  1    @1 CAMICIOLI (Richard)
A11 05  1    @1 FREI (Karen)
A11 06  1    @1 GITELMAN (Darren)
A11 07  1    @1 GOLDMAN (Jennifer)
A11 08  1    @1 GROWDON (John)
A11 09  1    @1 HURTIG (Howard I.)
A11 10  1    @1 LEVIN (Bonnie)
A11 11  1    @1 LITVAN (Irene)
A11 12  1    @1 MARSH (Laura)
A11 13  1    @1 SIMUNI (Tanya)
A11 14  1    @1 TRÖSTER (Alexander I.)
A11 15  1    @1 UC (Ergun Y.)
A14 01      @1 Departments of Neurology and Neurosurgery, University of Michigan @2 Ann Arbor, Michigan @3 USA @Z 1 aut.
A14 02      @1 VA Boston Healthcare System and Department of Psychiatry, Boston University School of Medicine @2 Boston, Massachusetts @3 USA @Z 2 aut.
A14 03      @1 Departments of Psychiatry and Neurology, Johns Hopkins University School of Medicine @2 Baltimore, Maryland @3 USA @Z 3 aut.
A14 04      @1 Division of Neurology, Department of Medicine, University of Alberta @2 Edmonton, Alberta @3 CAN @Z 4 aut.
A14 05      @1 The Parkinson's and Movement Disorders Institute @2 Fountain Valley, California @3 USA @Z 5 aut.
A14 06      @1 Departments of Neurology and Radiology, Northwestern University Feinberg School of Medicine @2 Chicago, Illinois @3 USA @Z 6 aut.
A14 07      @1 Department of Neurological Sciences, Rush University Medical Center @2 Chicago, Illinois @3 USA @Z 7 aut.
A14 08      @1 Department of Neurology, Massachusetts General Hospital @2 Boston, Massachusetts @3 USA @Z 8 aut.
A14 09      @1 Depratment of Neurology, University of Pennsylvania Health System @2 Philadelphia, Pennsylvania @3 USA @Z 9 aut.
A14 10      @1 Department of Neurology, University of Miami Miller School of Medicine @2 Miami, Florida @3 USA @Z 10 aut.
A14 11      @1 Department of Neurology, University of Louisville School of Medicine @2 Louisville, Kentucky @3 USA @Z 11 aut.
A14 12      @1 Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine @2 Houston, Texas @3 USA @Z 12 aut.
A14 13      @1 Parkinson's Disease and Movement Disorders Center and Department of Neurology, Northwestern University Feinberg School of Medicine @2 Chicago, Illinois @3 USA @Z 13 aut.
A14 14      @1 Department of Neurology, University of North Carolina-Chapel Hill @2 Chapel Hill, North Carolina @3 USA @Z 14 aut.
A14 15      @1 Department of Neurology, University of Iowa @2 Iowa City, Iowa @3 USA @Z 15 aut.
A14 16      @1 Veterans Affairs Medical Center @2 Iowa City, Iowa @3 USA @Z 15 aut.
A17 01  1    @1 Parkinson Study Group Cognitive/Psychiatric Working Group @3 INC
A20       @1 2501-2507
A21       @1 2010
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000191411680040
A44       @0 0000 @1 © 2010 INIST-CNRS. All rights reserved.
A45       @0 33 ref.
A47 01  1    @0 10-0512923
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 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.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Maladie de Parkinson @2 NM @5 01
C03 01  X  ENG  @0 Parkinson disease @2 NM @5 01
C03 01  X  SPA  @0 Parkinson enfermedad @2 NM @5 01
C03 02  X  FRE  @0 Trouble cognitif @5 02
C03 02  X  ENG  @0 Cognitive disorder @5 02
C03 02  X  SPA  @0 Trastorno cognitivo @5 02
C03 03  X  FRE  @0 Pathologie du système nerveux @5 03
C03 03  X  ENG  @0 Nervous system diseases @5 03
C03 03  X  SPA  @0 Sistema nervioso patología @5 03
C03 04  X  FRE  @0 Dépistage @5 09
C03 04  X  ENG  @0 Medical screening @5 09
C03 04  X  SPA  @0 Descubrimiento @5 09
C03 05  X  FRE  @0 Essai clinique @5 10
C03 05  X  ENG  @0 Clinical trial @5 10
C03 05  X  SPA  @0 Ensayo clínico @5 10
C07 01  X  FRE  @0 Pathologie de l'encéphale @5 37
C07 01  X  ENG  @0 Cerebral disorder @5 37
C07 01  X  SPA  @0 Encéfalo patología @5 37
C07 02  X  FRE  @0 Syndrome extrapyramidal @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Maladie dégénérative @5 39
C07 03  X  ENG  @0 Degenerative disease @5 39
C07 03  X  SPA  @0 Enfermedad degenerativa @5 39
C07 04  X  FRE  @0 Pathologie du système nerveux central @5 40
C07 04  X  ENG  @0 Central nervous system disease @5 40
C07 04  X  SPA  @0 Sistema nervosio central patología @5 40
N21       @1 347
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 10-0512923 INIST
ET : A Recommended Scale for Cognitive Screening in Clinical Trials of Parkinson's Disease
AU : CHOU (Kelvin L.); AMICK (Melissa M.); BRANDT (Jason); CAMICIOLI (Richard); FREI (Karen); GITELMAN (Darren); GOLDMAN (Jennifer); GROWDON (John); HURTIG (Howard I.); LEVIN (Bonnie); LITVAN (Irene); MARSH (Laura); SIMUNI (Tanya); TRÖSTER (Alexander I.); UC (Ergun Y.)
AF : Departments of Neurology and Neurosurgery, University of Michigan/Ann Arbor, Michigan/Etats-Unis (1 aut.); VA Boston Healthcare System and Department of Psychiatry, Boston University School of Medicine/Boston, Massachusetts/Etats-Unis (2 aut.); Departments of Psychiatry and Neurology, Johns Hopkins University School of Medicine/Baltimore, Maryland/Etats-Unis (3 aut.); Division of Neurology, Department of Medicine, University of Alberta/Edmonton, Alberta/Canada (4 aut.); The Parkinson's and Movement Disorders Institute/Fountain Valley, California/Etats-Unis (5 aut.); Departments of Neurology and Radiology, Northwestern University Feinberg School of Medicine/Chicago, Illinois/Etats-Unis (6 aut.); Department of Neurological Sciences, Rush University Medical Center/Chicago, Illinois/Etats-Unis (7 aut.); Department of Neurology, Massachusetts General Hospital/Boston, Massachusetts/Etats-Unis (8 aut.); Depratment of Neurology, University of Pennsylvania Health System/Philadelphia, Pennsylvania/Etats-Unis (9 aut.); Department of Neurology, University of Miami Miller School of Medicine/Miami, Florida/Etats-Unis (10 aut.); Department of Neurology, University of Louisville School of Medicine/Louisville, Kentucky/Etats-Unis (11 aut.); Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine/Houston, Texas/Etats-Unis (12 aut.); Parkinson's Disease and Movement Disorders Center and Department of Neurology, Northwestern University Feinberg School of Medicine/Chicago, Illinois/Etats-Unis (13 aut.); Department of Neurology, University of North Carolina-Chapel Hill/Chapel Hill, North Carolina/Etats-Unis (14 aut.); Department of Neurology, University of Iowa/Iowa City, Iowa/Etats-Unis (15 aut.); Veterans Affairs Medical Center/Iowa City, Iowa/Etats-Unis (15 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2010; Vol. 25; No. 15; Pp. 2501-2507; Bibl. 33 ref.
LA : Anglais
EA : 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.
CC : 002B17; 002B17G
FD : Maladie de Parkinson; Trouble cognitif; Pathologie du système nerveux; Dépistage; Essai clinique
FG : Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central
ED : Parkinson disease; Cognitive disorder; Nervous system diseases; Medical screening; Clinical trial
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease
SD : Parkinson enfermedad; Trastorno cognitivo; Sistema nervioso patología; Descubrimiento; Ensayo clínico
LO : INIST-20953.354000191411680040
ID : 10-0512923

Links to Exploration step

Pascal:10-0512923

Le document en format XML

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<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.</div>
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<ET>A Recommended Scale for Cognitive Screening in Clinical Trials of Parkinson's Disease</ET>
<AU>CHOU (Kelvin L.); AMICK (Melissa M.); BRANDT (Jason); CAMICIOLI (Richard); FREI (Karen); GITELMAN (Darren); GOLDMAN (Jennifer); GROWDON (John); HURTIG (Howard I.); LEVIN (Bonnie); LITVAN (Irene); MARSH (Laura); SIMUNI (Tanya); TRÖSTER (Alexander I.); UC (Ergun Y.)</AU>
<AF>Departments of Neurology and Neurosurgery, University of Michigan/Ann Arbor, Michigan/Etats-Unis (1 aut.); VA Boston Healthcare System and Department of Psychiatry, Boston University School of Medicine/Boston, Massachusetts/Etats-Unis (2 aut.); Departments of Psychiatry and Neurology, Johns Hopkins University School of Medicine/Baltimore, Maryland/Etats-Unis (3 aut.); Division of Neurology, Department of Medicine, University of Alberta/Edmonton, Alberta/Canada (4 aut.); The Parkinson's and Movement Disorders Institute/Fountain Valley, California/Etats-Unis (5 aut.); Departments of Neurology and Radiology, Northwestern University Feinberg School of Medicine/Chicago, Illinois/Etats-Unis (6 aut.); Department of Neurological Sciences, Rush University Medical Center/Chicago, Illinois/Etats-Unis (7 aut.); Department of Neurology, Massachusetts General Hospital/Boston, Massachusetts/Etats-Unis (8 aut.); Depratment of Neurology, University of Pennsylvania Health System/Philadelphia, Pennsylvania/Etats-Unis (9 aut.); Department of Neurology, University of Miami Miller School of Medicine/Miami, Florida/Etats-Unis (10 aut.); Department of Neurology, University of Louisville School of Medicine/Louisville, Kentucky/Etats-Unis (11 aut.); Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine/Houston, Texas/Etats-Unis (12 aut.); Parkinson's Disease and Movement Disorders Center and Department of Neurology, Northwestern University Feinberg School of Medicine/Chicago, Illinois/Etats-Unis (13 aut.); Department of Neurology, University of North Carolina-Chapel Hill/Chapel Hill, North Carolina/Etats-Unis (14 aut.); Department of Neurology, University of Iowa/Iowa City, Iowa/Etats-Unis (15 aut.); Veterans Affairs Medical Center/Iowa City, Iowa/Etats-Unis (15 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2010; Vol. 25; No. 15; Pp. 2501-2507; Bibl. 33 ref.</SO>
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<EA>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.</EA>
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