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Clinical Trials/NCT02106949
NCT02106949CompletedPhase 3

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

University Hospital, Brest13 sites in 1 country530 target enrollmentStarted: August 20, 2014Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
530
Locations
13
Primary Endpoint
Number of suicide reattempts in every group
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

SMS

Experimental

The patients of the test group receive a first SMS 48 hours after their discharge from the hospital then a total of 10 messages distributed over six months: 48 hours, S1, S2, M1, M2, M3, M4, M5, M6 and M13.

Intervention: SMS contact with patient after discharge in intervention group (Device)

Without SMS

No Intervention

The patients of the group benefit from the usual care.

Outcomes

Primary Outcomes

Number of suicide reattempts in every group

Time Frame: 6 months

Secondary Outcomes

  • Number of suicide reattempts in every group(13 months)
  • 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)
  • Total number of suicidal second recurrences in every group(13 months)
  • Number of deaths by suicide(6 months and 13 months)
  • Total number of suicidal second recurrences in every group(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (13)

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Short Message System (SMS) Monitoring... | Clinical Trial