Evaluation of a safety plan to prevent repeated suicide attempts
Official title: Evaluation of the Effectiveness of the Implementation of a Safety Plan by the Emergency Nurse to Prevent Suicidal Reiteration - National Multicenter Randomized Controlled Trial in Stepped-wedge
Run by Hôpital le Vinatier · NCT05609487 · Data updated 2026-11-12
This study is testing a safety plan created by nurses to see if it can help people who have recently tried to take their own lives avoid doing it again in the next six months.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 2387 (estimated) |
| Sponsor | Hôpital le Vinatier Academic / other |
| Locations | 1 site (Bron, AURA) |
| Status | Recruiting |
| Started | September 25, 2023 |
| Main results expected | January 15, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | September 19, 2024 |
| Trial ID | NCT05609487 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 and older who have recently attempted suicide and are seen in an emergency department.
✕Probably not a fit
Patients who are hospitalized for more than 24 hours following their suicide attempt or those under protective measures may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of a safety plan implemented by emergency department nurses for patients who have recently attempted suicide. The safety plan, developed in the United States, consists of a list of personalized strategies to help individuals manage suicidal thoughts. The goal is to determine if this intervention leads to a significant reduction in the likelihood of subsequent suicide attempts within six months compared to standard care. Participants will be included in the Vigilans program, which aims to prevent suicidal recurrence.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the risk of repeated suicide attempts among at-risk individuals.
How similar studies have gone: Previous studies in the United States have shown promising results with similar safety plan interventions, indicating potential for success in this context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years of age or older * Seen in an emergency department * Admitted in emergency department following a suicide attempt \<48h * whose duration of care does not exceed 24 hours * For whom the care project results in a return home, * Who agree to be included in the Vigilans system * Who have social security coverage * Fluent in French Exclusion Criteria: * Refusal to participate in the study * Refusal to be accompanied by the Vigilans system * Hospitalisation for more than 24 hours in the immediate aftermath of the suicide attempt * Under protective measures.
Where it's running
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Centre Hospitalier Le Vinatier
Bron, Aura, France Recruiting
Study contacts
- Principal investigator: Benoit Chalancon, Ide — Ch Le Vinatier
- Study coordinator: Benoit Chalancon, Ide
- Email: benoit.chalancon@ch-le-vinatier.fr
- Phone: 0033437915210
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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SAFETY family-based program for youths after a suicide attempt
This project will test whether the SAFETY family-based therapy helps 10-17-year-olds who recently attempted suicide avoid repeat attempts.
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Multi-layered digital monitoring and pharmacogenomics to prevent suicide in adults with depression
This study tests whether a digital monitoring system, a digital safety plan, and pharmacogenetic-guided care can reduce suicide re-attempts in adults with depression.
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Mindfulness-based programs for suicidal thoughts and self-harm in Korean youth
We will test whether two mindfulness-based programs for Korean adolescents and young adults reduce suicidal thoughts, self-harm, depression, and problems with sleep and emotion regulation.
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Youth suicide risk factors and personalized reduction strategies in young adults
This study tests whether combining clinical data, genetic information, neuroimaging, and microbiome data can help identify risk factors and see if a dTMS-based intervention reduces suicide risk in young adults with mood disorders.
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Long-term follow-up of depression in psychiatric care
This project will follow 415 people with difficult-to-treat depression who were previously studied to see how their symptoms and treatment outcomes change over five years.
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Improving coping to reduce suicide risk after ED discharge
This study tests whether an electronic safety plan and supportive text messages can help adults who have recently had suicidal thoughts or behaviors after leaving the emergency department.
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.