Combined peer support, personalized Hope Box, and postcard follow-up for suicidal inpatients
Official title: Peer-Aid and Hope Box: A Feasibility Study of a Combined Intervention for Suicidal Patients Hospitalized in a Psychiatric Crisis Unit
Run by Hôpital le Vinatier · NCT07119671 · Data updated 2026-11-12
This project will try a combined program of a peer helper meeting, a personalized Hope Box, and a reminder postcard to help people hospitalized after a recent suicide attempt.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 42 (estimated) |
| Sponsor | Hôpital le Vinatier Academic / other |
| Locations | 1 site (Bron, AURA) |
| Status | Recruiting |
| Started | September 24, 2025 |
| Main results expected | October 15, 2028 |
| Study ends | October 15, 2029 |
| Registry record updated | April 21, 2026 |
| Trial ID | NCT07119671 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are French-speaking adults hospitalized in a psychiatric crisis unit within 24–48 hours of admission who have made a suicide attempt in the month before hospitalization and can give informed consent and receive mail.
✕Probably not a fit
Patients with agitation, acute delirium, major cognitive disorder or other relational states incompatible with the intervention, those enrolled in another suicide-prevention protocol, or those without sufficient French language or postal access are unlikely to benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
HOPAIR is a mixed-methods feasibility project that enrolls patients 24–48 hours after admission to a psychiatric crisis unit and delivers a one-on-one meeting with a trained peer helper who helps the patient create a personalized Hope Box. The Hope Box contains objects, photos and reminders intended to strengthen reasons for living and provide sensory comfort, and a postcard is sent one month later to reinforce the intervention. The study is bi-centric and collects quantitative measures at three months on hopelessness, self-efficacy, reasons for living, perceived social support, suicidal thoughts and repeat attempts, alongside qualitative feedback on acceptability and implementation. The primary aim is to determine whether this combined intervention can be delivered and accepted in the inpatient crisis setting.
Why it matters
Potential benefit: If successful, HOPAIR could improve hope, coping and social connection and reduce acute suicidal thoughts or repeat attempts during a high-risk period after hospitalization.
How similar studies have gone: Brief contact interventions and peer-support approaches have shown promise in suicide prevention, but the specific combination of peer support, a Hope Box and a follow-up postcard is relatively novel and not widely tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Major ; * Hospitalized in a psychiatric crisis unit; * Having attempted suicide in the month preceding hospitalisation; * Able to give free and informed consent; * Having given consent; * French-speaking person with at least B1 level (reading and writing); * With access to the technical resources required for the study; * With a postal address. Exclusion Criteria: * Presenting a relational modality incompatible with the proposed intervention (agitation, acute delirium, major cognitive disorders or psychic disorganisation, etc.); * Included in another research protocol related to suicide prevention.
Where it's running
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Centre Hospitalier Le Vinatier
Bron, Aura, France Recruiting
Study contacts
- Principal investigator: Tamara VERNET, IPA — Centre Hospitalier le Vinatier
- Study coordinator: Tamara VERNET, IPA
- Email: Tamara.vernet@ch-le-vinatier.fr
- Phone: 00334 37 91 52 10
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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.