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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03991806
Other study ID # 2020-1844
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 31, 2020
Est. completion date August 31, 2025

Study information

Verified date February 2024
Source Jewish General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the frailty and the health adverse events in the population of the Canadian Longitudinal Study on Aging. It will be used the Centre of Excellence Self-Administered questionnaire (CESAM) which assesses frailty of older adults by providing a score and a of frailty in 4 levels.


Description:

Age is broadly recognized to confer a risk for health adverse outcomes, but it is an insensitive and non-specific measure for use in individual decision-making. Frailty has been emerging to take its rightful place as a better measure for over past decades. Despite general consensus that the concept of frailty is clinically useful, the lack of agreement on its definition and the challenge of its measurement by front-line health providers mean that frailty remains only 'their apparent' to chronological age as a criterion to select older persons at risk.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 30000
Est. completion date August 31, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - Being 65 years and over - Being enrolled in the Canadian Longitudinal Study on Aging Exclusion Criteria: - Never being enrolled in the Canadian Longitudinal Study on Aging - Undisclosed health adverse events

Study Design


Intervention

Other:
Obsservational
The frailty and the health adverse events of older adults will be assessed by using a questionnaire called: Association of Centre of Excellence Self-Administered questionnaire (CESAM).

Locations

Country Name City State
Canada Jewish General Hospital Montréal Quebec

Sponsors (1)

Lead Sponsor Collaborator
Jewish General Hospital

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dementia The algorithm is a three- step process involving administration of the neuropsychological battery to develop composite score in the three domains-memory, executive function, and psychomotor speed.
The primary outcome of the study will be to determine the number of participants to whom the memory, the executive function, and the psychomotor speed are affected.
around 18 months
Secondary Medication In the maintaining contact interview, one question will be asked of all participants in relation to prescription medication use in the preceding month. A second question asks about the frequency of prescription drug use during this month.
The secondary outcome of the study will be to determine the number of the medication that the participant take during a period of time.
around 18 months
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