Status:
UNKNOWN
Bae: A Smartphone Application for a Better Following Adolescents at Risk of Suicidal Behavior: Study of Acceptability and Preliminary Results of Efficacy
Lead Sponsor:
University Hospital, Montpellier
Collaborating Sponsors:
University Hospital, Lille
University Hospital, Nîmes
Conditions:
Suicide Attempt
Suicidal Ideation
Eligibility:
All Genders
12-17 years
Phase:
NA
Brief Summary
Suicidal behavior among adolescents is a major public health problem. Exacerbation of suicidal risk most often occurs when the young person is in his or her natural environment, far from the health ca...
Detailed Description
100 patients having recently attempted suicide or having suicidal ideation will be recruited. They will be asked to use the application bae during 6 months and will be followed up during this period. ...
Eligibility Criteria
Inclusion
- Criteria for inclusion
- All subjects will be required to meet the following inclusion criteria:
- Having consulted in the context of a suicidal crisis according to the criteria defined according to the consensus conference of the High Authority of Health (HAS 2000) ("psychic crisis for which the major risk is suicide. It can be represented as the trajectory that goes from the pejorative feeling of being in a situation of failure to a perceived impossibility of escaping this impasse. It is accompanied by suicidal ideas that become more and more pervasive and pervasive until the eventual act is carried out") in the previous 7 days.
- Possess a compatible smartphone (operating system: iOs or Androïd)
- Subject affiliated to or beneficiary of a French social security scheme
- Be able to understand the nature, purpose and methodology of the study
- Informed consent signed by the patient and his/her parent(s) or legal representative(s)
- Exclusion Criteria:
- Patient deprived of liberty (by judicial or administrative decision)
- Inability to understand, speak and write French
- Participation in another study with an exclusion period.
Exclusion
Key Trial Info
Start Date :
September 20 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 11 2022
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT04686162
Start Date
September 20 2021
End Date
July 11 2022
Last Update
August 11 2021
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