- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06441877
Community Spirit in Residence for the Elderly (437_EsCom)
April 17, 2025 updated by: TOPMED
The Elder at the Heart of His or Her Living Environment - Social Participation and Community Spirit in Residence for the Elderly
The objective of our study is to observe and understand factors that emphasizes the creation of a community spirit.
Specific objectives:
- Explore and understand the facilitators and challenges of social participation in a residential context;
- Explore and understand the facilitators and challenges of creating a sense of community in a residential setting.
Study Overview
Study Type
Observational
Enrollment (Actual)
27
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
-
Québec, Quebec, Canada, G1S 1C1
- Topmed
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Elderly home care residents and the managers that work on site.
The participants will be sampled from the selected community homes.
Description
Inclusion Criteria:
For site managers
- Be a manager in the residences concerned
- Be a department manager or
- Hold a General Manager position or
- Be a member of the partner's head office
For residents
- Residents of the autonomous wing of the targeted residences
- Close caregiver of a resident of the residences included in the research project
Exclusion Criteria:
- Neurocognitive disorders
- Significant language difficulties
- Lack of verbal communication
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Residents site 1
Elderly residents who live in elderly home care service site 1
|
There is no intervention, this is an observationnal study.
|
|
Residents site 2
Elderly residents who live in elderly home care service site 2
|
There is no intervention, this is an observationnal study.
|
|
Managers site 1
Managers who work for the elderly home care service at site 1
|
There is no intervention, this is an observationnal study.
|
|
Managers site 2
Managers who work for the elderly home care service at site 2
|
There is no intervention, this is an observationnal study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sense of Community Factors
Time Frame: Up to 1 month after participants' recruitment
|
13 items questionnaire with open questions in individual interview session format, factors are identified through qualitative analysis.
|
Up to 1 month after participants' recruitment
|
|
Sense of Community
Time Frame: Up to two weeks prior to the interview session
|
9 items questionnaire used to measure the sense of community of the residents.
For managers, the measure is their perception of the resident's sense of community.
Each item uses a 5 point scale, higher score means higher sense of community, minimum value per item: 1, maximum value per item: 5, minimum total score: 9, maximum total score : 45
|
Up to two weeks prior to the interview session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sense of Community Facilitators
Time Frame: Up to 1 month after participants' recruitment
|
7 subitems asked in the questionnaire with open questions in individual interview session format, facilitators are identified through qualitative analysis.
|
Up to 1 month after participants' recruitment
|
|
Sense of Community Obstacles
Time Frame: Up to 1 month after participants' recruitment
|
8 subitems asked in the questionnaire with open questions in individual interview session format, obstacles are identified through qualitative analysis.
|
Up to 1 month after participants' recruitment
|
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)
May 7, 2024
Primary Completion (Actual)
June 4, 2024
Study Completion (Actual)
January 14, 2025
Study Registration Dates
First Submitted
May 3, 2024
First Submitted That Met QC Criteria
June 3, 2024
First Posted (Actual)
June 4, 2024
Study Record Updates
Last Update Posted (Actual)
April 20, 2025
Last Update Submitted That Met QC Criteria
April 17, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 437_Esprit communauté
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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