- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03962985
Effects of Montreal Museum of Fine Arts Visits and Older Community Dwellers With a Precarious State
July 22, 2024 updated by: Olivier Beauchet, Jewish General Hospital
Effects of Montreal Museum of Fine Arts Visits and Older Community Dwellers With a Precarious State: An Experimental Study
This study evaluates the effects of MMFA visits on psychological, health, social conditions and personal interactions in older community dwellers with a precarious state and to determine whether these effects may change precarity.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Precarity is a vulnerable state exposing individuals to adverse health, psychological social events.
Older adults are exposed to precarity, especially those who were the old generation of immigrants in Canada.
Art-based activities have also been proposed to community dwellers and have shown positive effects on health outcomes and are determinants for well-being with aging.
The effects of participatory art-based activities on precarity in older adults have never been examined.
Recently, the Montreal Museum of Fine Arts (MMFA) developed a new participatory art-based activity which is a 3 month-period of weekly museum visits for precarious populations.
Study Type
Interventional
Enrollment (Actual)
41
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Quebec
-
Montréal, Quebec, Canada, H3T 1E2
- Jewish General Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years and older (Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Being 65 years and over;
- Precarious condition defined with a score ≥30 (/100)
- Having an Internet access with an electronic device (i.e.; laptop, computer, smartphone, tablet) as the repetitive assessments for this study will be performed on the web platform of the Centre of Excellence on Longevity of McGill University;
- Understanding and writing the different languages of the recruitment centre (i.e., French, English, Chinese.);
- Severe frail condition determined with the Centre of Excellence self-administered questionnaire (CESAM)
- Living in Montreal
Exclusion Criteria:
- A concomitant participation to another clinical trial;
- Participation in another art-based activity;
- Palliative care;
- Living in residence;
- Having a moderate to severe mobility impairment (i.e. using a walker, a wheelchair or being unable to walk alone 10m).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Intervention
The 41 participants will attend the guided tours at the Montreal Museum of Fine Arts.
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Precarious social conditions
Time Frame: 3 months
|
It will be used a questionnaire called: Evaluation of Health Precariousness and Inequalities in Health Examination Centers(EPICE).
This questionnaire has 11 questions that summarize 90% a precarious state.
The answer to each question is assigned a coefficient, the sum of the 11 answers gives the EPICES score.
The score is continuous and ranges from 0 (no precarious social conditions) to 100 (maximum level of precarious conditions).The threshold of 30 defined a precarious state.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Well-being
Time Frame: 3 months
|
It will be used a questionnaire called: Warwick-Edinburgh Mental Well-being Scale questionnaire (WEMWBS).The Warwick-Edinburgh Mental Well-being Scale questionnaire is a validated questionnaire composed by 14 positively worded item scale with five response categories.
It covers most aspects of positive mental health (positive thoughts and feelings).
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Olivier Beauchet, MD, Jewish General Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 23, 2019
Primary Completion (Actual)
June 1, 2022
Study Completion (Actual)
July 1, 2024
Study Registration Dates
First Submitted
May 23, 2019
First Submitted That Met QC Criteria
May 23, 2019
First Posted (Actual)
May 24, 2019
Study Record Updates
Last Update Posted (Actual)
July 23, 2024
Last Update Submitted That Met QC Criteria
July 22, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2020-1789
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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