- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02106949
Short Message System (SMS) Monitoring Intended for the Suicidal Patients
January 22, 2025 updated by: University Hospital, Brest
Short Message System (SMS) Monitoring Intended for the Suicidal Patients: Study of Efficiency
The study wants to prove that SMS monitoring reduced the number of suicide attempts in six months according to the beginning of its implementation in the group of the patients benefiting SMS compared with the group of patients benefiting from the usual care.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
530
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Angers, France
- CHU Angers
-
Brest, France, 29609
- CHRU de Brest
-
Caen, France
- CHU Caen
-
Lille, France
- CHRU Lille
-
Lyon, France
- CHU de Lyon
-
Nantes, France
- CHU Nantes
-
Quimperlé, France
- CH Quimperlé
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Rennes, France
- Chu Rennes
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Saint Etienne, France, 42055
- CHU de Saint-Etienne, Hôpital Nord
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St Malo, France, 35403
- CH St Malo
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St Nazaire, France
- CHU St Nazaire
-
Tours, France
- CHU Tours
-
Vannes, France
- CH Vannes
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Written informed consent
- Surviving a suicide attempt
- Leaving directly the emergency department or hospitalized less than 7 days
- Being able to be joined by telephone mobile
Exclusion Criteria:
- under guardianship
- Patient who are not able to provide a consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: SMS
The patients of the test group receive a first SMS 48 hours after their discharge from the hospital then a total of 10 messages distributed over six months: 48 hours, S1, S2, M1, M2, M3, M4, M5, M6 and M13.
|
|
|
No Intervention: Without SMS
The patients of the group benefit from the usual care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of suicide reattempts in every group
Time Frame: 6 months
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Number of suicide reattempts in every group
Time Frame: 13 months
|
13 months
|
|
Total number of suicidal second recurrences in every group
Time Frame: 6 months
|
6 months
|
|
Total number of suicidal second recurrences in every group
Time Frame: 13 months
|
13 months
|
|
Number of deaths by suicide
Time Frame: 6 months and 13 months
|
6 months and 13 months
|
|
Score in the scale C-SSRS
Time Frame: inclusion, 6 months and 13 months
|
inclusion, 6 months and 13 months
|
|
Presence of a disorder in the MINI: characterization of the comorbidity
Time Frame: 6 months and 13 months
|
6 months and 13 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Berrouiguet S, Alavi Z, Vaiva G, Courtet P, Baca-Garcia E, Vidailhet P, Gravey M, Guillodo E, Brandt S, Walter M. SIAM (Suicide intervention assisted by messages): the development of a post-acute crisis text messaging outreach for suicide prevention. BMC Psychiatry. 2014 Nov 18;14:294. doi: 10.1186/s12888-014-0294-8.
- Witt KG, Hetrick SE, Rajaram G, Hazell P, Taylor Salisbury TL, Townsend E, Hawton K. Psychosocial interventions for self-harm in adults. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013668. doi: 10.1002/14651858.CD013668.pub2.
- Berrouiguet S, Larsen ME, Mesmeur C, Gravey M, Billot R, Walter M; HUGOPSY Network; Lemey C, Lenca P. Toward mHealth Brief Contact Interventions in Suicide Prevention: Case Series From the Suicide Intervention Assisted by Messages (SIAM) Randomized Controlled Trial. JMIR Mhealth Uhealth. 2018 Jan 10;6(1):e8. doi: 10.2196/mhealth.7780.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 20, 2014
Primary Completion (Actual)
March 22, 2019
Study Completion (Actual)
March 22, 2019
Study Registration Dates
First Submitted
April 4, 2014
First Submitted That Met QC Criteria
April 4, 2014
First Posted (Estimated)
April 8, 2014
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 22, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SIAM
- RB 13-068 [CHRU Brest]
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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