- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07620418
CapExchange: A Pilot Feasibility Study of a Capacity-Exchange Programme for Mental Health Recovery (CapExchange)
June 24, 2026 updated by: EPSM de la Guadeloupe
CapExchange: Study Protocol for a Pilot Feasibility Study of a Capacity-Exchange Programme for Mental Health Recovery
CapExchange is a psychosocial rehabilitation programme based on reciprocal exchange of capacities and services between service users and their community environment, grounded in the concepts of circular mutuality and micro-social contribution.
This pilot feasibility study aims to assess the feasibility and acceptability of the programme within the Psychosocial Rehabilitation Service of the EPSM de la Guadeloupe, across three sites: the Unité Passerelle, the CATTG Doubs, and the UREPS outpatient unit.
A sample of 10 to 15 adult service users with a stabilized mental disorder is targeted.
The intervention comprises five weekly group sessions of 75 minutes.
Primary measures include the Social Contribution Score (SCS) and the Warwick-Edinburgh Mental Well-being Scale (WEMWBS).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
15
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 Contact
- Name: Ilyass El Mahfoudi, MD
- Phone Number: +33608342789
- Email: ilyass.elmahfoudi@epsm-guadeloupe.fr
Study Locations
-
-
-
Saint-Claude, Guadeloupe, 97190
- EPSM de la Guadeloupe
-
Contact:
- Ilyass El Mahfoudi, MD
- Phone Number: +33608342789
- Email: ilyass.elmahfoudi@epsm-guadeloupe.fr
-
-
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
No
Description
Inclusion Criteria:
- Adults aged 18 years or over
- Stabilized mental disorder (no acute episode in the 3 months preceding inclusion)
- At least one identifiable practical skill exchangeable in a community context
- Free and informed consent to participation
Exclusion Criteria:
- Severe clinical instability at the time of inclusion
- Uncontrolled risk behaviour in social interactions
- Documented inability to engage in a reciprocity-based framework
- Opposition from legal guardian for service users under legal protection'
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: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: CapExchange Programme
Five weekly group sessions of 75 minutes based on reciprocal exchange of capacities and services between service users and their community environment.
|
A structured group programme comprising five weekly sessions of 75 minutes based on reciprocal exchange of capacities and services between service users and their community environment, grounded in the concepts of circular mutuality and micro-social contribution.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Recruitment rate
Time Frame: 3 months
|
Proportion of eligible service users agreeing to participate in the programme
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ilyass El Mahfoudi, MD, EPSM Guadeloupe
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 (Estimated)
January 4, 2027
Primary Completion (Estimated)
September 15, 2027
Study Completion (Estimated)
December 20, 2027
Study Registration Dates
First Submitted
May 27, 2026
First Submitted That Met QC Criteria
May 27, 2026
First Posted (Actual)
June 2, 2026
Study Record Updates
Last Update Posted (Actual)
June 29, 2026
Last Update Submitted That Met QC Criteria
June 24, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CapExchange-2026-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be shared given the pilot and feasibility nature of this study and the small sample size.
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.