Skip to content

Museum Prescription by a Physician for a Visit to the MBAM

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05445453
Acronym
PM
Enrollment
86
Registered
2022-07-06
Start date
2022-06-27
Completion date
2023-12-22
Last updated
2024-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of Life, Social Isolation

Keywords

Arts, Well-being, Mental Health

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.

Interventions

The intervention is a visit of the MMFA. This visit can be done alone or accompanied. The visit of the MMFA is free for the patient.

Sponsors

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

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

This study is experimental, prospective, open-label, non-randomized, pre-post intervention with a single group of participants who will be their own control.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
Quality of life3 monthsQuality 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.
Well-being3 monthsWell-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.

Secondary

MeasureTime frameDescription
Physical Health Status3 monthsPhysical health status will be assessed using the CRIUGM Self-AdMinistered questionnaire (CESAM). The CESAM has been previously developed and validated. It is composed of 20 items exploring several domains: * weight loss and its extent; * polypharmacy defined by a number of therapeutic classes taken on a daily basis ≥ 5; * vision, hearing, and memory problems; * use of home support; * 6-item activities of daily living scale, 4-item instrumental activities of daily living scale; * mood assessed * regular physical activity defined as at least 1 hour per week in the past month; * and history of falls in the past 12 months. The CESAM provides two complementary scores: 1. An overall frailty score ranging from 0 to 18 2. A four-stage categorization of frailty This questionnaire will be completed online on the CRIUGM web platform using an electronic device.
Social Isolation3 monthsSocial isolation will be assessed using the 11-item Duke Social Support Index (DSSI). This index includes two subscales: * social interaction (i.e., frequency of interactions) * subjective support (i.e., satisfaction with emotional support provided). The DSSI score ranges from 11 to 33, with higher scores indicating higher levels of social inclusion. Scores for the 11 items are combined and categorized as low (score ≤26), high (score 27-29), and very high (score 30-33). We will use the mean score of the 11-item DSSI and its breakdown into three categories as the primary outcome. This questionnaire will be completed online on the CRIUGM web platform using an electronic device.
Prescribing context3 monthsResearchers will also study the prescribing context. A document will be filled by primary care physicians to give additional informations on the prescribing context such as the date of the prescription and the reason of the prescription.
Satisfaction from the visit to the museum3 monthsA short questionnaire will be given to participants to the intervention at the end of the visit to the museum. This questionnaire will give additionnal information on the satisfaction from the visit and whether the visit was made alone or accompanied.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026