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

University Hospital, Brest1 site in 1 country15 target enrollmentJuly 19, 2017

ConditionsPrevention of the Suicide

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Prevention of the Suicide
Sponsor: University Hospital, Brest
Enrollment: 15
Locations: 1
Primary Endpoint: Measurement of the feasibility of the device by the patient according to a validated questionnaire
Status: Completed
Last Updated: 5 months ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

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.

Registry

clinicaltrials.gov

Start Date

July 19, 2017

End Date

August 8, 2019

Last Updated

5 months ago

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

University Hospital, Brest

Responsible Party

Sponsor

Eligibility Criteria

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.

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

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