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

Sponsor

University Hospital, Brest (Other)

Overall Status

Completed

CT.gov ID

NCT03069560

Collaborator

(none)

Enrollment

Location

Arm

24.6

Actual Duration (Months)

0.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Prevention of the Suicide	Device: SMS	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

15 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Prevention

Official Title:

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

Actual Study Start Date :

Jul 19, 2017

Actual Primary Completion Date :

Aug 8, 2019

Actual Study Completion Date :

Aug 8, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 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.	Device: SMS SMS contact from the caregiver with patient after discharge in intervention group

Arm

Intervention/Treatment

Experimental: 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.

Device: SMS

SMS contact from the caregiver with patient after discharge in intervention group

Outcome Measures

Primary Outcome Measures

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

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
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.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

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.