TAPAS: The Life Paths That Lead Teenagers to Attempted Suicide:Trajectories of Proximal Adversity

Sponsor
University Hospital, Lille (Other)
Overall Status
Recruiting
CT.gov ID
NCT04638205
Collaborator
(none)
120
1
36
3.3

Study Details

Study Description

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).

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    120 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Retrospective
    Official Title:
    The Life Paths That Lead Teenagers to Attempted Suicide: Trajectories of Proximal Adversity
    Actual Study Start Date :
    Nov 1, 2019
    Anticipated Primary Completion Date :
    Nov 1, 2022
    Anticipated Study Completion Date :
    Nov 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    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

    Outcome Measures

    Primary Outcome Measures

    1. Growth parameters of the patterns of proximal adverse trajectories in adolescents who attempted suicide, as compared to non-suicidal adolescents [1 year]

      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

    Secondary Outcome Measures

    1. Statistical tests comparing the sociodemographic, vulnerabily and psychopathological indicators between the sub-group of adolescents identified from the mixture model. [1 year]

      Growth mixture models will allow for identifying sub-groups of individuals who are similar as regards to their burden of adversity trajectories. We will compare the characteristics of theses subgroups

    2. Growth parameters of the patterns of evolution of psychological pain [1 year]

      Parallel to the burden of adversity growth models, we will build, for each group, growth models to predict the longitudinal evolution of psychological pain. We will then test whether the growth parameters of the ideation/pain trajectories correlate with those of the adversity trajectories

    3. Growth parameters of the patterns of evolution of suicidal ideation intensity [1 year]

      Parallel to the burden of adversity growth models, we will build, for each group, growth models to predict the longitudinal evolution of the severity of the suicidal ideations. We will then test whether the growth parameters of the ideation/pain trajectories correlate with those of the adversity trajectories

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 24 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Inclusion criteria for cases

    • 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

    • Who gave their informed consent for majors, or whose parents gave their informed consent for minors Inclusion criteria for controls

    • Youth aged 15-24 inclusive

    • Who have never experienced any suicidal ideation or suicide attempt

    • Who gave their informed consent for majors, or whose parents gave their informed consent for minors Inclusion criteria for informants

    • 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

    Exclusion Criteria:
    • No consent or consent withdrawal for majors and/or their parents for minors

    • Neurological or psychiatric condition altering the capacity to understand

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hop Fontan - Chu Lille Lille France 59037

    Sponsors and Collaborators

    • University Hospital, Lille

    Investigators

    • Principal Investigator: Charles-Edouard Notredame, MD, University Hospital, Lille

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Lille
    ClinicalTrials.gov Identifier:
    NCT04638205
    Other Study ID Numbers:
    • 2018_20
    • 2018-A03065-50
    First Posted:
    Nov 20, 2020
    Last Update Posted:
    Mar 2, 2022
    Last Verified:
    Feb 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by University Hospital, Lille
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 2, 2022