Actively Recruiting
Feasibility Study of a Combined Intervention for Suicidal Inpatients in Psychiatric Crisis Units.
Led by Hôpital le Vinatier · Updated on 2026-04-21
42
Participants Needed
1
Research Sites
211 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Since 2014, suicide prevention has been a national priority and is one of the 3 priority areas of the mental health plan's roadmap . Hospitalization offers a crucial opportunity for life-preserving intervention . Brief health interventions and contacts are reputed to be easy to implement, effective and inexpensive . The Hope Box is a practical emotional management tool that aims to encourage the expression of reasons for living by materializing them in a customizable box, filled with objects, photos, writings and memories in order to find comfort and hope . Peer support use their experiential knowledge of disorders and recovery to accompany people and help humanize care . They can play a decisive role in suicide prevention . In contrast to an approach focusing only on risk factors, peer support and the Hope Box are both focus on protective factors, the strengths of the people concerned and hope. The primary objective of this study is to evaluate the feasibility of the HOPAIR intervention (peer-support and Hope Box, completed by a reminder postcard) with suicidal people hospitalized in psychiatric crisis units. Its secondary objective is to assess the potential effectiveness on intensity of hopelessness, sense of self-efficacy, reasons for living, perceived social support and suicidal recurrence at 3 months. This is a mixed-methods study involving 40 patients and 2 peer support in two crisis hospitalization units.
CONDITIONS
Official Title
Feasibility Study of a Combined Intervention for Suicidal Inpatients in Psychiatric Crisis Units.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult (18 years or older)
- Hospitalized in a psychiatric crisis unit
- Attempted suicide within one month before hospitalization
- Able to give free and informed consent
- Provided consent to participate
- French-speaking person with at least B1 level in reading and writing
- Access to required technical resources for the study
- Have a postal address
You will not qualify if you...
- Having agitation, acute delirium, major cognitive disorders, or severe psychic disorganization incompatible with the intervention
- Currently participating in another suicide prevention research protocol
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Centre Hospitalier Le Vinatier
Bron, AURA, France, 69678 CEDEX
Actively Recruiting
Research Team
T
Tamara VERNET, IPA
CONTACT
V
Veronique VIAL
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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