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Goal Management Training for Parkinson Disease Mild Cognitive Impairment

Primary Purpose

Parkinson Disease, Mild Cognitive Impairment

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Goal Management Training
Psychoeducation
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Parkinson Disease focused on measuring Mild Cognitive Impairment, Parkinson Disease, Cognitive Intervention, Goal Management Training, Executive Functions

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. PD diagnosis from the United Kingdom Research Brain Bank diagnostic criteria for PD (Hughes et al., 1992);
  2. PD-MCI diagnosis from the Movement Disorder Society Task Force diagnostic criteria. Single and multiple-domain MCI were both included, only if executive functions were significantly impaired (-1 standard deviation on executive function tests according to age and education-adjusted norms);
  3. Montreal Cognitive Assessment scores between 21 and 27;
  4. Anti-Parkinson medication stable (at screening) since at least two months;
  5. All other medications, including psychotropics, stable for at least three months.

Exclusion Criteria:

  1. Participants with PD and dementia diagnosis
  2. Patients with other neurological or psychiatric disorders.

Sites / Locations

  • School of Psychology

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Goal Management Training

Psychoeducation sessions coupled mindfulness exercises

Arm Description

GMT modules were adapted for French-speaking patients with PD-MCI. Each session was reduced from nine 90-120-minute sessions (original GMT) to five 60-90-minute sessions, one session per week, in order to avoid fatigue. As for original GMT, participants were given exercises between sessions (mindfulness exercises and metacognitive reflections). In original-GMT, some information is repeated several times, but not in Adapted-GMT. Exercises demanding motor dexterity, such as card distribution, were removed. Adapted-GMT included information on PD-MCI and executive dysfunction (some psychoeducation). In addition, Adapted-GMT modules were administered individually with an iPad, as opposed to a power-point group presentation in original-GMT. A workbook was handed to participants, as in previous studies.

Five modules were designed as a discussion with patients and caregivers about various PD symptoms: module I-brain and motor symptoms; module II-autonomic symptoms; module III- psychological symptoms; module IV-brain and cognition; and module V-cognitive impairments in PD. Patients were handed the information book about the five modules at the beginning of the study. The objective was to improve their understanding of their condition and to discuss other components that could affect their cognitive abilities. After the 40-60-minute informative part, mindfulness exercises were offered for 20-30 minutes per session. Participants were not invited to practice exercises between sessions, but 3/6 participants reported they did.

Outcomes

Primary Outcome Measures

Raw score Change from baseline DEX (self rated) to 3 weeks after beginning of intervention
Questionnaire on subjective executive functions
Raw score Change from baseline DEX (self rated) to 1 week post test
Questionnaire on subjective executive functions
Raw score Change from baseline DEX (self rated) to 4 weeks post test
Questionnaire on subjective executive functions
Raw score Change from baseline DEX (self rated) to 12 weeks post test
Questionnaire on subjective executive functions
Raw score Change from baseline DEX (caregiver rated) to 3 weeks after the beginning of intervention
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Raw score Change from baseline DEX (caregiver rated) to 1 week post test
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Raw score Change from baseline DEX (caregiver rated) to 4 weeks post test
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Raw score Change from baseline DEX (caregiver rated) to 12 weeks post test
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Raw score Change from baseline Zoo Map Test to 1 week post test
Neuropsychological test assessing planification and organisation
Raw score Change from baseline Zoo Map Test to 4 weeks post test
Neuropsychological test assessing planification and organisation
Raw score Change from baseline Zoo Map Test to 12 weeks post test
Neuropsychological test assessing planification and organisation

Secondary Outcome Measures

Raw score Change from baseline Parkinson Disease Questionnaire (39 items; PDQ-39) to 3 weeks after the beginning of intervention
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Raw score Change from baseline PDQ-39 to 1 week post-test
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Raw score Change from baseline PDQ-39 to 4 weeks post-test
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Raw score Change from baseline PDQ-39 to 12 weeks post-test
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Mean Change from baseline Dementia Rating Scale, 2nd edition (DRS-II) to 1 week post-test
A brief neuropsychological instrument designed to assess general cognitive functioning
Mean Change from baseline Dementia Rating Scale, 2nd edition (DRS-II) to 4 weeks post-test
A brief neuropsychological instrument designed to assess general cognitive functioning
Mean Change from baseline Dementia Rating Scale, 2nd edition (DRS-II) to 12 weeks post-test
A brief neuropsychological instrument designed to assess general cognitive functioning
Raw score Change from baseline Zarit Burden Interview (12 items) to 3 weeks after the beginning of intervention
A 12-item questionnaire assessing the feeling of burden of the caregiver
Raw score Change from baseline Zarit Burden Interview (12 items) to 1 week post-test
A 12-item questionnaire assessing the feeling of burden of the caregiver
Raw score Change from baseline Zarit Burden Interview (12 items) to 4 weeks post-test
A 12-item questionnaire assessing the feeling of burden of the caregiver
Raw score Change from baseline Zarit Burden Interview (12 items) to 12 week post-test
A 12-item questionnaire assessing the feeling of burden of the caregiver
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 3 weeks after the beginning of intervention (mid-point)
assessment of twelve neuropsychiatric symptoms usually found in dementia
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 1 week post-test
assessment of twelve neuropsychiatric symptoms usually found in dementia
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 4 weeks post-test
assessment of twelve neuropsychiatric symptoms usually found in dementia
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 12 weeks post-test
assessment of twelve neuropsychiatric symptoms usually found in dementia
Raw score Change from baseline Apathy Evaluation Scale (AES) to 3 weeks after the beginning of intervention (mid-point)
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Raw score Change from baseline Apathy Evaluation Scale (AES) to 1 week post-test
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Raw score Change from baseline Apathy Evaluation Scale (AES) to 4 weeks post-test
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Raw score Change from baseline Apathy Evaluation Scale (AES) to 12 weeks post-test
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).

Full Information

First Posted
October 30, 2020
Last Updated
November 16, 2020
Sponsor
Laval University
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1. Study Identification

Unique Protocol Identification Number
NCT04636541
Brief Title
Goal Management Training for Parkinson Disease Mild Cognitive Impairment
Official Title
Goal Management Training Home-Based Approach for Cognitive Impairment in Parkinson's Disease: A Single-Blind Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
April 30, 2018 (Actual)
Primary Completion Date
July 20, 2019 (Actual)
Study Completion Date
July 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Laval University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Mild cognitive impairment is experienced by approximately 30% of patients with Parkinson's disease (PD-MCI), often affecting executive functions. There is currently no pharmacological treatment available for PD-MCI and non-pharmacological treatments are still scarce. The aim of this study was to test preliminary efficacy/effectiveness of two home-based cognitive interventions adapted for patients with PD-MCI: Goal Management Training, adapted for PD-MCI (Adapted-GMT), and a psychoeducation program combined with mindfulness exercises. Twelve persons with PD-MCI with executive dysfunctions, as measured by extensive neuropsychological evaluation, were randomly assigned to one of two intervention groups. Both groups received five sessions each lasting 60-90 minutes for five weeks, in presence of the caregiver. Measures were collected at baseline, mid-point, at one-week, four-week and 12-week follow-ups. Primary outcomes were executive functions assessed by subjective (DEX questionnaire patient- and caregiver-rated) and objective (Zoo Map Test) measures. Secondary outcomes included quality of life (PDQ-39), global cognition (DRS-II), and neuropsychiatric symptoms (NPI-12). Safety data (fatigue, medication change and compliance) were also recorded. Repeated measures ANCOVAs were applied to outcomes. Both groups significantly ameliorated executive functions overtime as indicated by improvements in DEX-patient and DEX-caregiver scores. PDQ-39 scores decreased at the four-week follow-up in the Psychoeducation/Mindfulness group whereas they were maintained in the Adapted-GMT group. All other measures were maintained over time in both groups. Adapted-GMT and Psychoeducation/Mindfulness groups both improved executive functioning. This is one of the first studies to test home-based approaches, tailored to the participant's cognitive needs, and involving caregivers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease, Mild Cognitive Impairment
Keywords
Mild Cognitive Impairment, Parkinson Disease, Cognitive Intervention, Goal Management Training, Executive Functions

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Comparison of two different cognitive intervention (two groups, randomized, single blinded)
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
The research was a single blind randomized comparative study. After the screening evaluation, participants were randomly assigned to either group A or B, described below (block randomization, three blocks of four participants).
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Goal Management Training
Arm Type
Experimental
Arm Description
GMT modules were adapted for French-speaking patients with PD-MCI. Each session was reduced from nine 90-120-minute sessions (original GMT) to five 60-90-minute sessions, one session per week, in order to avoid fatigue. As for original GMT, participants were given exercises between sessions (mindfulness exercises and metacognitive reflections). In original-GMT, some information is repeated several times, but not in Adapted-GMT. Exercises demanding motor dexterity, such as card distribution, were removed. Adapted-GMT included information on PD-MCI and executive dysfunction (some psychoeducation). In addition, Adapted-GMT modules were administered individually with an iPad, as opposed to a power-point group presentation in original-GMT. A workbook was handed to participants, as in previous studies.
Arm Title
Psychoeducation sessions coupled mindfulness exercises
Arm Type
Active Comparator
Arm Description
Five modules were designed as a discussion with patients and caregivers about various PD symptoms: module I-brain and motor symptoms; module II-autonomic symptoms; module III- psychological symptoms; module IV-brain and cognition; and module V-cognitive impairments in PD. Patients were handed the information book about the five modules at the beginning of the study. The objective was to improve their understanding of their condition and to discuss other components that could affect their cognitive abilities. After the 40-60-minute informative part, mindfulness exercises were offered for 20-30 minutes per session. Participants were not invited to practice exercises between sessions, but 3/6 participants reported they did.
Intervention Type
Behavioral
Intervention Name(s)
Goal Management Training
Intervention Description
Goal Management Training® (GMT) has been developed to improve executive functions. It was validated in patients presenting executive dysfunction following many conditions: acquired traumatic brain injury, neurodevelopmental spina bifida, attention deficit and hyperactivity disorder (ADHD), subjective cognitive complaints and multiple sclerosis. GMT includes self-instruction strategies, self-monitoring exercises, cognitive training techniques, psychoeducation on cognitive processes, mindfulness exercises and assignments between sessions. It has been shown to increase patient awareness of deficits and improve cognitive control in goal-directed behaviors. The original GMT is a nine-week program administered to dysexecutive patients in 90-to-120-minute group sessions. Thus, it might be suitable for PD-MCI patients presenting with executive dysfunction.
Intervention Type
Behavioral
Intervention Name(s)
Psychoeducation
Intervention Description
See the Arm section for full details. For a justification of how we designed this intervention: Many clinical guidelines include general recommendations about giving information to PD patients and family so they can take part into decision process. However, few standardized psychoeducation interventions are available, and they don't include information on PD cognitive decline. Some studies investigated Mindfulness Based Stress Reduction (MBSR) and other related mindfulness interventions in PD patients. In this approach, formal meditative exercises are included to develop non-judgmental attention to experiences in the present moment. In elderly patients with MCI unrelated to PD, mindfulness interventions show positive effects on cognitive functioning, including attention, executive functioning and memory (Gard et al., 2014). Therefore, non-pharmacological interventions for PD-MCI including both education on cognitive symptoms, as well as mindfulness exercises, are promising.
Primary Outcome Measure Information:
Title
Raw score Change from baseline DEX (self rated) to 3 weeks after beginning of intervention
Description
Questionnaire on subjective executive functions
Time Frame
3 weeks after beginning of intervention (mid-point)
Title
Raw score Change from baseline DEX (self rated) to 1 week post test
Description
Questionnaire on subjective executive functions
Time Frame
1 week post-test
Title
Raw score Change from baseline DEX (self rated) to 4 weeks post test
Description
Questionnaire on subjective executive functions
Time Frame
4 weeks post-test
Title
Raw score Change from baseline DEX (self rated) to 12 weeks post test
Description
Questionnaire on subjective executive functions
Time Frame
12 weeks post-test
Title
Raw score Change from baseline DEX (caregiver rated) to 3 weeks after the beginning of intervention
Description
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Time Frame
3 weeks after beginning of intervention (mid-point)
Title
Raw score Change from baseline DEX (caregiver rated) to 1 week post test
Description
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Time Frame
1 week post-test
Title
Raw score Change from baseline DEX (caregiver rated) to 4 weeks post test
Description
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Time Frame
4 weeks post-test
Title
Raw score Change from baseline DEX (caregiver rated) to 12 weeks post test
Description
Questionnaire on subjective executive functions (caregiver rates the executive functions of the participant
Time Frame
12 weeks post-test
Title
Raw score Change from baseline Zoo Map Test to 1 week post test
Description
Neuropsychological test assessing planification and organisation
Time Frame
1 week post-test
Title
Raw score Change from baseline Zoo Map Test to 4 weeks post test
Description
Neuropsychological test assessing planification and organisation
Time Frame
4 weeks post-test
Title
Raw score Change from baseline Zoo Map Test to 12 weeks post test
Description
Neuropsychological test assessing planification and organisation
Time Frame
12 weeks post-test
Secondary Outcome Measure Information:
Title
Raw score Change from baseline Parkinson Disease Questionnaire (39 items; PDQ-39) to 3 weeks after the beginning of intervention
Description
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Time Frame
3 weeks after beginning of intervention (mid-point of intervention)
Title
Raw score Change from baseline PDQ-39 to 1 week post-test
Description
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Time Frame
1 week post-test
Title
Raw score Change from baseline PDQ-39 to 4 weeks post-test
Description
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Time Frame
4 weeks post-test
Title
Raw score Change from baseline PDQ-39 to 12 weeks post-test
Description
Self rated questionnaire on quality of life with symptoms of Parkinson Disease
Time Frame
12 weeks post-test
Title
Mean Change from baseline Dementia Rating Scale, 2nd edition (DRS-II) to 1 week post-test
Description
A brief neuropsychological instrument designed to assess general cognitive functioning
Time Frame
1 week post-test
Title
Mean Change from baseline Dementia Rating Scale, 2nd edition (DRS-II) to 4 weeks post-test
Description
A brief neuropsychological instrument designed to assess general cognitive functioning
Time Frame
4 weeks post-test
Title
Mean Change from baseline Dementia Rating Scale, 2nd edition (DRS-II) to 12 weeks post-test
Description
A brief neuropsychological instrument designed to assess general cognitive functioning
Time Frame
12 weeks post-test
Title
Raw score Change from baseline Zarit Burden Interview (12 items) to 3 weeks after the beginning of intervention
Description
A 12-item questionnaire assessing the feeling of burden of the caregiver
Time Frame
3 weeks after the beginning of intervention (mid-point)
Title
Raw score Change from baseline Zarit Burden Interview (12 items) to 1 week post-test
Description
A 12-item questionnaire assessing the feeling of burden of the caregiver
Time Frame
1 week post-test
Title
Raw score Change from baseline Zarit Burden Interview (12 items) to 4 weeks post-test
Description
A 12-item questionnaire assessing the feeling of burden of the caregiver
Time Frame
4 weeks post-test
Title
Raw score Change from baseline Zarit Burden Interview (12 items) to 12 week post-test
Description
A 12-item questionnaire assessing the feeling of burden of the caregiver
Time Frame
Baseline, mid-point of intervention, 1 week post-test, 4 weeks post-test and 12 weeks post-test
Title
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 3 weeks after the beginning of intervention (mid-point)
Description
assessment of twelve neuropsychiatric symptoms usually found in dementia
Time Frame
3 weeks after the beginning of intervention (mid-point)
Title
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 1 week post-test
Description
assessment of twelve neuropsychiatric symptoms usually found in dementia
Time Frame
1 week post-test
Title
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 4 weeks post-test
Description
assessment of twelve neuropsychiatric symptoms usually found in dementia
Time Frame
4 week post-test
Title
Raw score Change from baseline Neuropsychiatric Inventory, 12 items to 12 weeks post-test
Description
assessment of twelve neuropsychiatric symptoms usually found in dementia
Time Frame
12 week post-test
Title
Raw score Change from baseline Apathy Evaluation Scale (AES) to 3 weeks after the beginning of intervention (mid-point)
Description
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Time Frame
3 weeks after the beginning of intervention (mid-point)
Title
Raw score Change from baseline Apathy Evaluation Scale (AES) to 1 week post-test
Description
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Time Frame
1 week post-test
Title
Raw score Change from baseline Apathy Evaluation Scale (AES) to 4 weeks post-test
Description
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Time Frame
4 weeks post-test
Title
Raw score Change from baseline Apathy Evaluation Scale (AES) to 12 weeks post-test
Description
An 18-item questionnaire assessing different aspects of apathy (cognitive, behavioral and emotional).
Time Frame
12 weeks post-test

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PD diagnosis from the United Kingdom Research Brain Bank diagnostic criteria for PD (Hughes et al., 1992); PD-MCI diagnosis from the Movement Disorder Society Task Force diagnostic criteria. Single and multiple-domain MCI were both included, only if executive functions were significantly impaired (-1 standard deviation on executive function tests according to age and education-adjusted norms); Montreal Cognitive Assessment scores between 21 and 27; Anti-Parkinson medication stable (at screening) since at least two months; All other medications, including psychotropics, stable for at least three months. Exclusion Criteria: Participants with PD and dementia diagnosis Patients with other neurological or psychiatric disorders.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martine Simard
Organizational Affiliation
Professor at Laval School of psychology
Official's Role
Study Director
Facility Information:
Facility Name
School of Psychology
City
Québec
ZIP/Postal Code
G1V0A6
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30412509
Citation
Clare L, Teale JC, Toms G, Kudlicka A, Evans I, Abrahams S, Goldstein LH, Hindle JV, Ho AK, Jahanshahi M, Langdon D, Morris R, Snowden JS, Davies R, Markova I, Busse M, Thompson-Coon J. Cognitive rehabilitation, self-management, psychotherapeutic and caregiver support interventions in progressive neurodegenerative conditions: A scoping review. NeuroRehabilitation. 2018;43(4):443-471. doi: 10.3233/NRE-172353.
Results Reference
background
PubMed Identifier
9153155
Citation
Cummings JL. The Neuropsychiatric Inventory: assessing psychopathology in dementia patients. Neurology. 1997 May;48(5 Suppl 6):S10-6. doi: 10.1212/wnl.48.5_suppl_6.10s.
Results Reference
background
PubMed Identifier
18098298
Citation
Dubois B, Burn D, Goetz C, Aarsland D, Brown RG, Broe GA, Dickson D, Duyckaerts C, Cummings J, Gauthier S, Korczyn A, Lees A, Levy R, Litvan I, Mizuno Y, McKeith IG, Olanow CW, Poewe W, Sampaio C, Tolosa E, Emre M. Diagnostic procedures for Parkinson's disease dementia: recommendations from the movement disorder society task force. Mov Disord. 2007 Dec;22(16):2314-24. doi: 10.1002/mds.21844.
Results Reference
background
PubMed Identifier
29951580
Citation
Goldman JG, Vernaleo BA, Camicioli R, Dahodwala N, Dobkin RD, Ellis T, Galvin JE, Marras C, Edwards J, Fields J, Golden R, Karlawish J, Levin B, Shulman L, Smith G, Tangney C, Thomas CA, Troster AI, Uc EY, Coyan N, Ellman C, Ellman M, Hoffman C, Hoffman S, Simmonds D. Cognitive impairment in Parkinson's disease: a report from a multidisciplinary symposium on unmet needs and future directions to maintain cognitive health. NPJ Parkinsons Dis. 2018 Jun 26;4:19. doi: 10.1038/s41531-018-0055-3. eCollection 2018.
Results Reference
background
PubMed Identifier
23126020
Citation
Grimes D, Gordon J, Snelgrove B, Lim-Carter I, Fon E, Martin W, Wieler M, Suchowersky O, Rajput A, Lafontaine AL, Stoessl J, Moro E, Schoffer K, Miyasaki J, Hobson D, Mahmoudi M, Fox S, Postuma R, Kumar H, Jog M; Canadian Nourological Sciences Federation. Canadian Guidelines on Parkinson's Disease. Can J Neurol Sci. 2012 Jul;39(4 Suppl 4):S1-30. doi: 10.1017/s031716710001516x. No abstract available.
Results Reference
background
PubMed Identifier
29314218
Citation
Hindle JV, Watermeyer TJ, Roberts J, Brand A, Hoare Z, Martyr A, Clare L. Goal-orientated cognitive rehabilitation for dementias associated with Parkinson's disease-A pilot randomised controlled trial. Int J Geriatr Psychiatry. 2018 May;33(5):718-728. doi: 10.1002/gps.4845. Epub 2018 Jan 4.
Results Reference
background
PubMed Identifier
1564476
Citation
Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry. 1992 Mar;55(3):181-4. doi: 10.1136/jnnp.55.3.181.
Results Reference
background
PubMed Identifier
8588541
Citation
Jenkinson C, Peto V, Fitzpatrick R, Greenhall R, Hyman N. Self-reported functioning and well-being in patients with Parkinson's disease: comparison of the short-form health survey (SF-36) and the Parkinson's Disease Questionnaire (PDQ-39). Age Ageing. 1995 Nov;24(6):505-9. doi: 10.1093/ageing/24.6.505.
Results Reference
background
PubMed Identifier
22275317
Citation
Litvan I, Goldman JG, Troster AI, Schmand BA, Weintraub D, Petersen RC, Mollenhauer B, Adler CH, Marder K, Williams-Gray CH, Aarsland D, Kulisevsky J, Rodriguez-Oroz MC, Burn DJ, Barker RA, Emre M. Diagnostic criteria for mild cognitive impairment in Parkinson's disease: Movement Disorder Society Task Force guidelines. Mov Disord. 2012 Mar;27(3):349-56. doi: 10.1002/mds.24893. Epub 2012 Jan 24.
Results Reference
background
PubMed Identifier
16965885
Citation
Macht M, Gerlich C, Ellgring H, Schradi M, Rusinol AB, Crespo M, Prats A, Viemero V, Lankinen A, Bitti PE, Candini L, Spliethoff-Kamminga N, de Vreugd J, Simons G, Pasqualini MS, Thompson SB, Taba P, Krikmann U, Kanarik E. Patient education in Parkinson's disease: Formative evaluation of a standardized programme in seven European countries. Patient Educ Couns. 2007 Feb;65(2):245-52. doi: 10.1016/j.pec.2006.08.005. Epub 2006 Sep 11.
Results Reference
background
PubMed Identifier
22689702
Citation
Matteau E, Dupre N, Langlois M, Provencher P, Simard M. Clinical validity of the Mattis Dementia Rating Scale-2 in Parkinson disease with MCI and dementia. J Geriatr Psychiatry Neurol. 2012 Jun;25(2):100-6. doi: 10.1177/0891988712445086.
Results Reference
background
PubMed Identifier
29747716
Citation
Roy MA, Doiron M, Talon-Croteau J, Dupre N, Simard M. Effects of Antiparkinson Medication on Cognition in Parkinson's Disease: A Systematic Review. Can J Neurol Sci. 2018 Jul;45(4):375-404. doi: 10.1017/cjn.2018.21. Epub 2018 May 11.
Results Reference
background
PubMed Identifier
29540124
Citation
Stamenova V, Levine B. Effectiveness of goal management training(R) in improving executive functions: A meta-analysis. Neuropsychol Rehabil. 2019 Dec;29(10):1569-1599. doi: 10.1080/09602011.2018.1438294. Epub 2018 Mar 14.
Results Reference
background
PubMed Identifier
25693688
Citation
Vlagsma TT, Koerts J, Fasotti L, Tucha O, van Laar T, Dijkstra H, Spikman JM. Parkinson's patients' executive profile and goals they set for improvement: Why is cognitive rehabilitation not common practice? Neuropsychol Rehabil. 2016;26(2):216-35. doi: 10.1080/09602011.2015.1013138. Epub 2015 Feb 19.
Results Reference
background
PubMed Identifier
26166188
Citation
Bora E, Walterfang M, Velakoulis D. Theory of mind in Parkinson's disease: A meta-analysis. Behav Brain Res. 2015 Oct 1;292:515-20. doi: 10.1016/j.bbr.2015.07.012. Epub 2015 Jul 9.
Results Reference
background
PubMed Identifier
11574710
Citation
Bedard M, Molloy DW, Squire L, Dubois S, Lever JA, O'Donnell M. The Zarit Burden Interview: a new short version and screening version. Gerontologist. 2001 Oct;41(5):652-7. doi: 10.1093/geront/41.5.652.
Results Reference
background
PubMed Identifier
1754629
Citation
Marin RS, Biedrzycki RC, Firinciogullari S. Reliability and validity of the Apathy Evaluation Scale. Psychiatry Res. 1991 Aug;38(2):143-62. doi: 10.1016/0165-1781(91)90040-v.
Results Reference
background
PubMed Identifier
28802929
Citation
Hiseman JP, Fackrell R. Caregiver Burden and the Nonmotor Symptoms of Parkinson's Disease. Int Rev Neurobiol. 2017;133:479-497. doi: 10.1016/bs.irn.2017.05.035. Epub 2017 Jul 21.
Results Reference
background
PubMed Identifier
30221586
Citation
Couture M, Giguere-Rancourt A, Simard M. The impact of cognitive interventions on cognitive symptoms in idiopathic Parkinson's disease: a systematic review. Neuropsychol Dev Cogn B Aging Neuropsychol Cogn. 2019 Sep;26(5):637-659. doi: 10.1080/13825585.2018.1513450. Epub 2018 Sep 17.
Results Reference
result
PubMed Identifier
30821637
Citation
Giguere-Rancourt A, Plourde M, Doiron M, Langlois M, Dupre N, Simard M. Goal management training (R) home-based approach for mild cognitive impairment in Parkinson's disease: a multiple baseline case report. Neurocase. 2018 Oct-Dec;24(5-6):276-286. doi: 10.1080/13554794.2019.1583345. Epub 2019 Mar 1.
Results Reference
result
PubMed Identifier
35180229
Citation
Giguere-Rancourt A, Plourde M, Racine E, Couture M, Langlois M, Dupre N, Simard M. Goal management training and psychoeducation / mindfulness for treatment of executive dysfunction in Parkinson's disease: A feasibility pilot trial. PLoS One. 2022 Feb 18;17(2):e0263108. doi: 10.1371/journal.pone.0263108. eCollection 2022.
Results Reference
derived

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Goal Management Training for Parkinson Disease Mild Cognitive Impairment

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