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Clinical Trials/NCT02106949
NCT02106949
Completed
Phase 3

Short Message System (SMS) Monitoring Intended for the Suicidal Patients: Study of Efficiency

University Hospital, Brest13 sites in 1 country530 target enrollmentAugust 20, 2014

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Patients Having Realized a Suicide Attempt
Sponsor
University Hospital, Brest
Enrollment
530
Locations
13
Primary Endpoint
Number of suicide reattempts in every group
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 20, 2014
End Date
March 22, 2019
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Number of suicide reattempts in every group

Time Frame: 6 months

Secondary Outcomes

  • 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)

Study Sites (13)

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