The Life Paths That Lead Teenagers to Attempted Suicide:Trajectories of Proximal Adversity
TAPAS
2 other identifiers
observational
39
1 country
1
Brief Summary
Suicidal behaviors seriously alter the vital and functional prognosis of adolescents. Although the literature has lighted out a considerable number of risk factors for suicide attempts in youth, theoretical models - among which bio-psycho-social models - still lack empirical evidence. More specifically, the way adverse life events dynamically interact together and with the individual's diathesis to precipitate suicidal attempts remains unclear. Studies of life trajectories have opened an alternative approach to traditional linear epidemiological analysis to capture such a complex process. To date, adverse trajectories approaches never have been applied to the period immediately preceding the occurrence of the suicidal gesture (proximal adverse trajectories).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2019
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2019
CompletedFirst Submitted
Initial submission to the registry
July 9, 2020
CompletedFirst Posted
Study publicly available on registry
November 20, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2022
CompletedDecember 26, 2025
December 1, 2025
3.2 years
July 9, 2020
December 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Growth parameters of the patterns of proximal adverse trajectories in adolescents who attempted suicide, as compared to non-suicidal adolescents
We will build growth mixture models to account for the 1-year longitudinal evolution of the Burden of Adversity values. Each group will be characterized by the parameters (intercepts and slopes) of the best-fitting model. We will the compare the parameters of the 2 groups to search for statistical differences
1 year
Secondary Outcomes (3)
Statistical tests comparing the sociodemographic, vulnerabily and psychopathological indicators between the sub-group of adolescents identified from the mixture model.
1 year
Growth parameters of the patterns of evolution of psychological pain
1 year
Growth parameters of the patterns of evolution of suicidal ideation intensity
1 year
Study Arms (2)
Suicide attempt cases
Adolescents and young adults who attempted suicide between 7 and 30 days prior the inclusion
Non-suicidal controls
Adolescents and young adults without history of suicide attempt or ideation
Eligibility Criteria
Patient recruitment will be supported by the VigilanS program. VigilanS is a suicide recurrence prevention device implemented in all establishments in the Hauts-de-France region that receive patients who have attempted suicide (www.dispositifvigilans.org).
You may qualify if:
- Youth aged 15-24 inclusive
- Who stayed at the hospital or in the emergency room for less than 15 days after a first suicide attempt
- Who were discharged less than 15 days ago
- Youth aged 15-24 inclusive
- Who have never experienced any suicidal ideation or suicide attempt
- Close relatives of the participant
- Who are major
- Who lived in the same household as the participant or have interacted with him/her for more than half the weeks of the year preceding the index suicide attempt
You may not qualify if:
- No consent or consent withdrawal for majors and/or their parents for minors
- Neurological or psychiatric condition altering the capacity to understand
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hop Fontan - Chu Lille
Lille, 59037, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Charles-Edouard Notredame, MD
University Hospital, Lille
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 9, 2020
First Posted
November 20, 2020
Study Start
November 1, 2019
Primary Completion
December 31, 2022
Study Completion
December 31, 2022
Last Updated
December 26, 2025
Record last verified: 2025-12