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

Not Applicable

Completed

• Conditions: Prevention of the Suicide

• Registration Number: NCT03069560
• Lead Sponsor: University Hospital, Brest

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-02-28
• Study First Submitted QC: 2017-03-02
• Study First Posted: 2017-03-03
• Study Start: 2017-07-19
• Primary Completion: 2019-08-08
• Study Completion: 2019-08-08
• Status Verified: 2020-05
• Last Update Submitted: 2020-05-18
• Last Update Posted: 2020-05-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 15

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Measurement of the feasibility of the device by the patient according to a validated questionnaire	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 Outcome Measures

Name	Time	Method
Qualitative analysis of messages sent to patients during the study.	6 months	A qualitative analysis of the messages addressed to the patients during the study will be carried out.
The questionnaire measuring the feasibility for the caregiver of such a device	6 months	A questionnaire will be provided to the caregiver to measure the feasibility of such a device
Questionnaires on the acceptability of patients and caregivers in relation to the use of this type of monitoring device	6 months	Acceptability questionnaires will be provided to patients and caregivers in relation to the use of this type of monitoring device

Trial Locations

Locations (1)

CHU de Brest; 🇫🇷 Brest, France