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Clinical Trials/NCT05445453
NCT05445453CompletedNot Applicable

Museum Prescription by a Physician for a Visit to the Montreal Museum of Fine Arts: Assessment of Effects.

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal2 sites in 1 country86 target enrollmentStarted: June 27, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
86
Locations
2
Primary Endpoint
Well-being

Study Overview

Brief Summary

In recent years, museums have participated in the patient care journey by using art to enhance their quality of life and well-being. Since 2015, the Montreal Museum of Fine Arts (MMFA) and Dr. Beauchet have developed an Action-Research program exploring the effects of participatory art activities for community elders conducted at the MMFA, known as the Arts & Longevity Lab (ALL). The mandate of ALL is to improve the well-being, quality of life and health (i.e. mental and physical state) of individuals and patients through the practice of visual arts activities (i.e. arts that produce objects perceived by the eyes).

Since 2019, the MMFA has developed in collaboration with Médecins Francophones du Canada museum visits prescribed by a primary care physician as a new intervention. Today, it is necessary to improve the knowledge on the effects of this museum visit prescription

The overall objective of this study is to examine the effects of a visit to the MMFA prescribed by a primary care physician on the mental health (well-being and quality of life) of patients living in Montreal.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • age 18 and over
  • having Internet access at home with an electronic device (computer, keyboard, or smartphone)
  • having no dementia
  • speaking English or French
  • committing to visiting the museum within 3 months of the prescription.

Exclusion Criteria

  • individuals participating in a clinical trial at the same time, to avoid interference with the results of the intervention being studied in this protocol
  • individuals with dementia. There are no tests for dementia. The physicians involved in the pre-recruitment process are aware of the cognitive status of their patients. Therefore, they will be able to avoid offering the study to a patient with dementia if such a diagnosis appears in the medical file.

Arms & Interventions

Intervention

Experimental

Physicians participating in the research project will be able to prescribe a visit to the Museum to any of their patients for whom they deem this museum prescription necessary. Only patients who meet the inclusion criteria will be offered to participate in the research.

If patients refuse or do not meet the inclusion criteria, they may be prescribed a museum visit but will not be offered the study.

After obtaining informed consent, the patient will be asked to complete 2 sets of self-administered questionnaires: in the 2 days prior to the visit and in the 2 days following the MBAM visit.

Intervention: Museum visit (Other)

Outcomes

Primary Outcomes

Well-being

Time Frame: 3 months

Well-being will be assessed using the Warwick-Edinburgh Mental Well-being Scale (WEMWBS). The WEMWBS is a validated questionnaire composed by a 14-item positively worded scale and five response categories. It covers most aspects of positive mental health (positive thoughts and feelings). This questionnaire will be completed online on the CRIUGM web platform using an electronic device.

Quality of life

Time Frame: 3 months

Quality of life will be assessed using the EuroQol-5D (EQ-5D). EuroQol-5D is composed of two parts: * a five-question questionnaire with a score per question ranging from 1 (no problem) to 5 (severe problem), so that the sum ranged from 0 (no problem) to 25 (severe problem). * a visual analogue scale on participants' perceived health. This scale is numbered from 0 (i.e., the worst health the participant can imagine) to 100 (i.e., the best health the participant can imagine). This questionnaire will be completed online on the CRIUGM web platform using an electronic device.

Secondary Outcomes

  • Physical Health Status(3 months)
  • Satisfaction from the visit to the museum(3 months)
  • Social Isolation(3 months)
  • Prescribing context(3 months)

Investigators

Sponsor
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Olivier Beauchet

MD, PhD, Senior researcher, Director of laboratory

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal

Study Sites (2)

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