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A Brief Case Management Intervention to Promote Personal Recovery and Prevent Psychiatric Involuntary Readmissions.

Study acronym: CARP-RCT
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Recruitment opened Show 5 more changesShow less
    • Primary and study completion dates: Nov 2029 to Dec 2029
    • Start date changed from estimate of Jun 2026 to Jul 1, 2026
    • Eligibility criteria expanded, about 7 words
    • Secondary endpoints: details revised at 18 of 18 entries
    • Site details revised
  2. Notable Start date: Apr 2026 to Jun 2026
    • Primary and study completion pushed from Sep 2029 to Nov 2029
    • Enrollment target: 252 to 262
    • Study description revised
    v3
  3. Minor Secondary endpoints: details revised at 3 of 18 entries
    • Study title shortened, about 4 words
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this randomized control trial is to assess the effectiveness of a Brief Case Management (BCM) intervention aimed at promoting personal recovery and reducing the negative effects of coercion among people involuntarily admitted to a psychiatric hospital. The main questions it aims to answer are : * Does the Brief Case Management intervention reduce the incidence of involuntary readmission18 months after the initial involuntary hospitalisation? * What impact does the Brief Case Management intervention have on patients' involuntary readmission 6 months after the initial involuntary hospitalisation, as well as on their personal recovery, perceived coercion, satisfaction with treatment, and on their exposure to other forms of formal and informal coercion? Participants will be randomly assigned to either the control or the intervention group, accordingly they will be asked to take part in: Control Group: * Three evaluation sessions (baseline, 6 and 18 months follow-up); Intervention Group : * Three evaluation sessions (baseline, 6 and 18 months follow-up); * The 5 sessions of the brief case management intervention (6th session optional).
Trial Details
NCT Number NCT07497763
Lead Sponsor Stéphane Morandi
Collaborators: University of Lausanne
Conditions
(from sponsor)
Psychiatric Disorder, Involuntary Psychiatric Hospitalization
Related terms Mental Disorders
Enrollment 262 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov