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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04052477
Other study ID # RECHMPL19_0320
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date December 30, 2020

Study information

Verified date September 2021
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

According to a recent and alarming WHO (World Health Organisation) report (September 4, 2014), one person dies of suicide every 40 seconds in the world. Suicide is the third-leading cause of death for 15- to 24-year-olds, according to the Centers for Disease Control and Prevention , after accidents and homicide. This major public health issue need prevention strategies especially directed to at-risk populations. Since 2013, more than 2 billion users are enrolled in social networks such as Twitter or Facebook. Young adults (ages 18 to 29) are the most likely to use social media - fully 90% do. Consequently, in this project, we focus on suicide prevention in social media network.. The aim of this project is the validation of the algorithm. This algorithm build a decision support system that monitor young people at-risk based on large volume of heterogeneous data collected through social media to improve suicide prevention.


Description:

This study is composed of two steps : 1. 9 subjects were recruited. After patients agreement, computer scientists were accessing to patient social network profile. Computer scientists were not able to visualize the content of publications, just run the algorithm that will analyse the content of messages (text, frequency, emoticons…) The algorithm defines the 3 most at-risk periods of suicide behaviors, on the next month. This result were compared to periods found by psychiatric interview. The psychiatrist then confirmed or not to LIRM whether periods found by the algorithm conrrespond to those defined by the psychitrist. No data of the social network were collected. 2. the 2nd step aim to improve the algorithm by collecting sociodemographic and clincal data related to patients included.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date December 30, 2020
Est. primary completion date June 1, 2017
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility Inclusion criteria: - Major patient - Minor patient with parents approval - Patient hospitalized due to suicide attempt or suicide ideations - Frequent active user of social netword (Facebook, Instagram, Youtube, Twitter) Exclusion criteria: - Patient's refusal to participate

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Montpellier LIRMM - Montpellier - France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary sensitivity of the algorithm baseline 1 day
See also
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Recruiting NCT06318962 - Examining the Efficacy of a Digital Therapeutic to Prevent Suicidal Behaviors N/A