Short Message System (SMS) for Caregivers of Suicidal Patients to Prevent Recidivism of Suicide Attempts
Not Applicable
Completed
- Conditions
- Prevention of the Suicide
- Interventions
- Device: SMS
- 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
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
- Arm && Interventions
Group Intervention Description SMS SMS 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.
- 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