Short Message System (SMS) Monitoring Intended for the Suicidal Patients
Phase 3
Completed
- Conditions
- Patients Having Realized a Suicide Attempt
- Registration Number
- NCT02106949
- Lead Sponsor
- University Hospital, Brest
- Brief Summary
The study wants to prove that SMS monitoring reduced the number of suicide attempts in six months according to the beginning of its implementation in the group of the patients benefiting SMS compared with the group of patients benefiting from the usual care.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 530
Inclusion Criteria
- Written informed consent
- Surviving a suicide attempt
- Leaving directly the emergency department or hospitalized less than 7 days
- Being able to be joined by telephone mobile
Exclusion Criteria
- under guardianship
- Patient who are not able to provide a consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Number of suicide reattempts in every group 6 months
- Secondary Outcome Measures
Name Time Method Presence of a disorder in the MINI: characterization of the comorbidity 6 months and 13 months Score in the scale C-SSRS inclusion, 6 months and 13 months Number of suicide reattempts in every group 13 months Total number of suicidal second recurrences in every group 13 months Number of deaths by suicide 6 months and 13 months
Trial Locations
- Locations (13)
CHU Angers
🇫🇷Angers, France
CHRU de Brest
🇫🇷Brest, France
CHU Caen
🇫🇷Caen, France
CHRU Lille
🇫🇷Lille, France
CHU de Lyon
🇫🇷Lyon, France
CHU Nantes
🇫🇷Nantes, France
CH Quimperlé
🇫🇷Quimperlé, France
CHU Rennes
🇫🇷Rennes, France
CHU de Saint-Etienne, Hôpital Nord
🇫🇷Saint Etienne, France
CH St Malo
🇫🇷St Malo, France
Scroll for more (3 remaining)CHU Angers🇫🇷Angers, France