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Short Message System (SMS) Monitoring Intended for the Suicidal Patients

R

Regional University Hospital Center (CHRU)

Status and phase

Completed
Phase 3

Conditions

Patients Having Realized a Suicide Attempt

Treatments

Device: SMS contact with patient after discharge in intervention group

Study type

Interventional

Funder types

Other

Identifiers

NCT02106949
SIAM
RB 13-068 [CHRU Brest]

Details and patient eligibility

About

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.

Enrollment

530 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

530 participants in 2 patient groups

SMS
Experimental group
Description:
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.
Treatment:
Device: SMS contact with patient after discharge in intervention group
Without SMS
No Intervention group
Description:
The patients of the group benefit from the usual care.

Trial contacts and locations

13

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Data sourced from clinicaltrials.gov

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