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Clinical Trials/NCT03069560
NCT03069560CompletedNot Applicable

Short Message System (SMS) for Caregivers of Suicidal Patients to Prevent Recidivism of Suicide Attempts

University Hospital, Brest2 sites in 1 country15 target enrollmentStarted: July 19, 2017Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
15
Locations
2
Primary Endpoint
Measurement of the feasibility of the device by the patient according to a validated questionnaire
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Assessment of the feasibility of a monitoring device by SMS in which messages are sent by the caregiver after a suicidal act.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • •Male or female, over 18 years of age and hospitalized;
  • •Survivor of a suicide attempt;
  • •Giving informed, dated and signed consent;
  • •Can be reached by mobile phone. The study is proposed to all adult suicides and to the patient's designated caregiver, meeting the inclusion criteria.

Exclusion Criteria

  • •Patient whose clinical condition is incompatible with the formulation of his non-opposition.
  • •The patient and his / her caregiver shall not be afforded a protective justice measure.

Arms & Interventions

SMS

Experimental

The patients will receive from the caregiver a first SMS 48 hours after their discharge from the hospital then a total of 4 messages : 48 hours, S1, S2, and S4.

Intervention: SMS (Device)

Outcomes

Primary Outcomes

Measurement of the feasibility of the device by the patient according to a validated questionnaire

Time Frame: 6 months

The primary endpoint is the measurement of the feasibility of the device by the patient based on a validated questionnaire. This evaluation will take place during the medical interview that will close the study participation.

Secondary Outcomes

  • The questionnaire measuring the feasibility for the caregiver of such a device(6 months)
  • Qualitative analysis of messages sent to patients during the study.(6 months)
  • Questionnaires on the acceptability of patients and caregivers in relation to the use of this type of monitoring device(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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