Brief Case Management to Help Personal Recovery after Involuntary Psychiatric Admission
Official title: A Brief Case Management Intervention to Promote Personal Recovery and Prevent Psychiatric Involuntary Readmissions: a Randomised Controlled Trial
Run by University of Lausanne Hospitals · NCT07497763 · Data updated 2026-11-12
This trial tests whether a Brief Case Management approach helps people who were involuntarily admitted to a psychiatric hospital recover personally and avoid another involuntary readmission.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 64 Years |
| Sex | All |
| Enrollment | 262 (estimated) |
| Sponsor | University of Lausanne Hospitals Academic / other |
| Locations | 1 site (Lausanne, Canton of Vaud) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | December 2029 |
| Study ends | December 2029 |
| Registry record updated | October 21, 2026 |
| Trial ID | NCT07497763 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18-64 who were involuntarily admitted for psychiatric care and live in the catchment area of the Canton of Vaud, speaking French well enough to participate.
✕Probably not a fit
Individuals with organic mental disorders, intellectual disability, inability to consent, or insufficient French proficiency may not benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares Brief Case Management plus treatment as usual to treatment as usual alone for adults (18-64) involuntarily admitted for psychiatric care in the Canton of Vaud. The study aims to see if BCM reduces involuntary readmissions at 6 and 18 months and improves personal recovery, perceived coercion, and satisfaction with treatment. Participants are followed with baseline, 6-month, and 18-month assessments. The intervention was developed with service-users and previously showed acceptable feasibility and satisfaction in a six-month pilot. The study is conducted at Lausanne University Hospital in Switzerland with the University of Lausanne as a collaborator.
Why it matters
Potential benefit: If successful, participants may experience better personal recovery and fewer involuntary readmissions.
How similar studies have gone: Prior work showed feasibility and satisfaction with the brief case management approach in a six-month pilot, but full effectiveness in reducing readmissions is being tested here.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * To have been involuntarily admitted by a medical doctor; * To be aged between 18 and 64 years; * To be domiciled in the catchment area of the Centre or West psychiatric sector of the Canton of Vaud; Exclusion Criteria: * Patients with an organic mental disorder (F0, ICD-10); * Patients with intellectual disability (F7, ICD-10); * Patients unable to provide written consent due to a lack of discernment; * Patients unable to speak French well enough to participate in the study without the help of an interpreter.
Where it's running
-
Lausanne University Hospital
Lausanne, Canton of Vaud, Switzerland Recruiting
Study contacts
- Principal investigator: Stéphane Morandi — Centre hospitalier universitaire vaudois (CHUV)
- Study coordinator: Stephane Morandi
- Email: stephane.morandi@chuv.ch
- Phone: +41 21 3140050
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.