Motoric Cognitive Risk and Depression
The Association of Depression With "Motoric Cognitive Risk" Syndrome in the Canadian Population
1 other identifier
observational
30,000
1 country
1
Brief Summary
The overall objective of the proposal is to examine the association between depression and the newly reported "motoric cognitive risk" (MCR) syndrome, which is a pre-dementia syndrome combining subjective cognitive complaint (i.e.; memory complaint) with objective slow gait speed, in the Canadian population, with the baseline assessment of the Canadian Longitudinal Study on Aging (CLSA). The Canadian and global population are continuously aging. Moreover, the number of individuals affected by dementia is on the rise. One good predictor of dementia is Motoric Cognitive Risk (MCR) syndrome. MCR syndrome is a highly prevalent, newly defined syndrome that combines slow gait and subjective cognitive complaint. Depression is also highly prevalent in the older population and can affect both cognition and gait. Thus, an overlap between MCR and depression is possible. Yet few studies have examined the association between MCR and depression, thus emphasizing the importance of further investigating this association. This project encompasses determining the association of MCR syndrome with depression in the Canadian context as a step to better understand MCR syndrome in Canada.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2019
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 18, 2018
CompletedFirst Posted
Study publicly available on registry
September 20, 2018
CompletedStudy Start
First participant enrolled
July 24, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedFebruary 23, 2024
February 1, 2024
5.3 years
September 18, 2018
February 22, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Subjective cognitive complaint
elicited from the 60-minute interview telephone questionnaire item Chronic Conditions Tracking (CTT\_19 CCT\_MEMPB\_TRM) done in CLSA study
1 hour
Secondary Outcomes (1)
Slow gait speed
1 day
Study Arms (4)
Group 45-54 years old
divided in two subgroups: individuals with and without cardio-vascular risk factors and diseases
Group 54-64 years old
divided in two subgroups: individuals with and without cardio-vascular risk factors and diseases
Group 65-74 years old
divided in two subgroups: individuals with and without cardio-vascular risk factors and diseases
Group 75-85 years old
divided in two subgroups: individuals with and without cardio-vascular risk factors and diseases
Interventions
telephone interview questionnaire, in-home face-to-face interview, and data from the Collection Site
Eligibility Criteria
Individuals eligible for this study will be the participants of the CLSA
You may qualify if:
- be participant of the comprehensive CLSA
You may not qualify if:
- dementia,
- mobility disability,
- no information about cognitive complaint,
- no measure of walking speed
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Jewish General Hospital
Montreal, Quebec, H3T 1E2, Canada
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Olivier Beauchet, MD
Jewish General Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor of Geriatrics
Study Record Dates
First Submitted
September 18, 2018
First Posted
September 20, 2018
Study Start
July 24, 2019
Primary Completion
October 31, 2024
Study Completion
December 1, 2025
Last Updated
February 23, 2024
Record last verified: 2024-02