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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04032145
Other study ID # 2020-1878
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 31, 2019
Est. completion date December 30, 2020

Study information

Verified date August 2021
Source Jewish General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the effects of arts on the Montreal Museum's clients.


Description:

Acting early in the process of weakening elders in order to keep them longer in good health and socially active is possible. During the past decade, museums have become involved in the care of patients by using art to improve their quality of life and well-being. Museums have, thus, emerged as new partners in public health. Very few programs developed by museums have focused on elders. Only one focused on elders in situation of early frailty and demonstrated that it was possible, through participatory visual art-based activities, to improve the health status of elders living at home.


Recruitment information / eligibility

Status Completed
Enrollment 316
Est. completion date December 30, 2020
Est. primary completion date December 30, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - Being 50 years old - Coming at Montreal Museum of Fine Arts for guided visits, arts activities, and so forth. Exclusion Criteria -No internet connection and electronic device like cell phone, Ipad or computer.

Study Design


Related Conditions & MeSH terms


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 Health Condition Health condition will be evaluates based on a questionnaire called: CESAM(Self Administered Questionnaire). This is an assessment questionnaire that each participant will answer once. The questionnaire is designed that participant's answers to questions are scored. After the answers are summed , the Principal Investigator will obtain an overall measure of participant' health condition. one month
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