NCT06036290

Brief Summary

The goal of this mixed-methods study is to describe the association between the level of parent/adolescent discordance in the assessment of the adolescent's level of suicidal intentionality after a suicid attempt and the evolution of the suicidal crisis by assessing the evolution of the adolescent's suicidal intentionality between T0 and 3 months. The main questions it aims to answer are:

  • To show the association between the level of parent/adolescent discordance in the assessment of the adolescent's level of suicidal intent after a suicid attempt and various markers of the evolution of the suicidal crisis at 3 months.
  • Explore the experience of adolescents and their parents regarding the elements they consider relevant in assessing the adolescent's suicidal intent. Participants will be asked to complete various self- and hetero-questionnaires at T0 and T3

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
160

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jul 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 27, 2023

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

August 8, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

September 13, 2023

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 27, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 27, 2025

Completed
Last Updated

September 13, 2023

Status Verified

September 1, 2023

Enrollment Period

1.8 years

First QC Date

August 8, 2023

Last Update Submit

September 12, 2023

Conditions

Suicidal IntentionSuicide, AttemptedParent-Child Relations

Outcome Measures

Primary Outcomes (1)

  • Difference in adolescents' level of suicidal intent

    Difference in adolescents' level of suicidal intent between T0 and 3 months. All measurements are based on a Visual Analogue Scale (VAS) graduated from 0 to 10.

    3 months

Secondary Outcomes (7)

  • Association between the level of parent/adolescent discordance in the assessment of the adolescent's level of suicidal intent after a suicidal attempt and various indicators of the evolution of the suicidal crisis at 3 months.

    3 months

  • association between the level of parent/adolescent discordance in assessing the adolescent's level of suicidal intent after a suicid attempt and the degree of family cohesion

    1 week

  • socio-familial factors associated with a high level of parent/adolescent discordance in assessing the adolescent's level of suicidal intentionality after a suicidal act.

    1 week

  • clinical factors associated with a high level of parent/adolescent discordance in assessing the adolescent's level of suicidal intent after a suicide attempt.

    1 week

  • evolution of the level of parent/adolescent discordance on the evaluation of the adolescent's level of suicidal intent after a suicide attempt at 0 and 3 months

    3 months

  • +2 more secondary outcomes

Eligibility Criteria

Age11 Years - 17 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)
Sampling MethodProbability Sample
Study Population

Adolescents: aged 11 to 17, admitted to a pediatric or adult emergency department following a suicide attempt. Parents: 18 years of age or older, parent or guardian of an adolescent admitted to a pediatric or adult emergency department following a suicide attempt.

You may qualify if:

  • Adolescents:
  • aged 11 to 17
  • admitted to a pediatric or adult emergency department following a suicide attempt
  • proficient in spoken French
  • not opposed to participation in the research
  • accompanied by at least one parent who is not opposed to the adolescent's participation in the research.
  • Parents:
  • years of age or older
  • parent or guardian of an adolescent admitted to a pediatric or adult emergency department following a suicide attempt
  • fluent in spoken French
  • not opposed to participation in the research

You may not qualify if:

  • present a decompensated somatic or psychiatric pathology or a vigilance disorder
  • refusal to participate in the research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Clermont-Ferrand

Clermont-Ferrand, France

RECRUITING

MeSH Terms

Conditions

Suicide, Attempted

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Central Study Contacts

Lise Laclautre

CONTACT

0promo_interne_drci@chu-clermontferrand.fr

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 8, 2023

First Posted

September 13, 2023

Study Start

July 27, 2023

Primary Completion

May 27, 2025

Study Completion

May 27, 2025

Last Updated

September 13, 2023

Record last verified: 2023-09

Data Sharing

IPD Sharing
Will not share

Locations

FR(1)