- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04310488
Assessment of Effects of Museum Prescription of A Montreal Museum of Fine Arts Visit Tour in Primary Care Patients
August 11, 2022 updated by: Olivier Beauchet, Jewish General Hospital
Assessment of Effects of Museum Prescription of A Montreal Museum Of Fine Arts Visit Tour in Primary Care Patients: a Cross-Sectional Study
The objective of this study is to examine effects on mental and physical health and quality of life in primary care patients visiting the Montreal Museum of Fine Arts (MMFA), this visit being prescribed by their physician.
To visit the MMFA and to complete after this visit a series of self-administered questionnaires within the two days after their visit at the museum
Study Overview
Status
Withdrawn
Conditions
Intervention / Treatment
Detailed Description
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 primary care patients who are a target audience for museum health program preventions.
For the development of appropriate museum programs based on visit tour, there is a need to improve knowledge the effects of a museum visit prescribed by a primary care physician in patients.
The objective of this study is to examine effects on mental and physical health and quality of life in primary care patients visiting the Montreal Museum of Fine Arts (MMFA), this visit being prescribed by their physician.
Based on a cross-sectional study it will be prescribed to all patients consulting their primary care physician to visit the MMFA and to complete after this visit a series of self-administered questionnaires within the two days after their visit at the museum.
The period of recruitment will be one year.
The outcomes are the scores of the different questionnaires.
Study Type
Observational
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
16 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Montreal Museum of Fine Arts visitors
Description
Inclusion Criteria:
- ≥ 18 years old
- Home Internet access with an electronic device (computer, pad or cellular phone)
- Patient without dementia
- Speak the language of the recruitment centre (French or English)
Exclusion Criteria:
- dementia
- participation refusal
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
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Socio-demographic characteristics from the primary care physician questionnaire
Time Frame: 1 day
|
Primary care physician questionnaire is composed of 12 items exploring socio demographic items (age, gender), the reason perceived by the participants of the prescription and the effects of the visit on a scale form 0 (not at all) to 10 (extremely)
|
1 day
|
Mental health condition from the primary care physician questionnaire
Time Frame: 1 day
|
Primary care physician questionnaire is composed of 12 items exploring socio demographic items (age, gender), the reason perceived by the participants of the prescription and the effects of the visit on a scale form 0 (not at all) to 10 (extremely)
|
1 day
|
Physical health condition
Time Frame: 1 day
|
The Centre of excellence self-administered (CESAM) questionnaire items
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 1, 2022
Primary Completion (Anticipated)
March 13, 2024
Study Completion (Anticipated)
March 13, 2025
Study Registration Dates
First Submitted
March 13, 2020
First Submitted That Met QC Criteria
March 13, 2020
First Posted (Actual)
March 17, 2020
Study Record Updates
Last Update Posted (Actual)
August 15, 2022
Last Update Submitted That Met QC Criteria
August 11, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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