NCT04638205

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
39

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2019

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

July 9, 2020

Completed
4 months until next milestone

First Posted

Study publicly available on registry

November 20, 2020

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2022

Completed
Last Updated

December 26, 2025

Status Verified

December 1, 2025

Enrollment Period

3.2 years

First QC Date

July 9, 2020

Last Update Submit

December 18, 2025

Conditions

Keywords

Suicide attemptadolescenceadverse life eventdevelopmental modeltrajectories

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

Age15 Years - 24 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

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

Location

MeSH Terms

Conditions

Suicide, Attempted

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Charles-Edouard Notredame, MD

    University Hospital, Lille

    PRINCIPAL INVESTIGATOR

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

Locations