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Clinical Trials/NCT06551038
NCT06551038
Recruiting
Not Applicable

Evaluating Primary Suicide Prevention in Adolescents With Risk Factors

Stephanie Baggio19 sites in 1 country240 target enrollmentMarch 11, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicide Prevention
Sponsor
Stephanie Baggio
Enrollment
240
Locations
19
Primary Endpoint
Composite measure of suicide awareness
Status
Recruiting
Last Updated
4 months ago

Overview

Brief Summary

Suicide is one of the main causes of death among teenagers. Because it is preventable, primary prevention of suicide has become a public health priority, with encouraging results in promoting suicide awareness and reducing suicidal thoughts among adolescents. However, the lack of studies conducted among vulnerable populations (i.e., marginalised, disengaged and disadvantaged) is a major gap, even though these populations present an increased risk of suicidal behaviour.

The aim of this project is to test the effectiveness of a brief primary suicide prevention intervention for vulnerable adolescents, using a randomised controlled trial. Vulnerable adolescents include those 1) detained in juvenile detention centres, 2) at risk of dropping out of school, 3) undergoing treatment for psychiatric disorders, 4) belonging to a sexual or gender diversity, 5) affected by chronic conditions, or 6) with relational/familial problems. The main aim is to test the effectiveness of the intervention on a composite measure of suicide awareness, psychological distress and suicidal thoughts. The project will also explore other issues that present challenges for vulnerable populations: access to primary suicide prevention and non-response bias. The study will provide relevant results to address the current lack of high-quality evidence for primary suicide prevention in adolescents.

Registry
clinicaltrials.gov
Start Date
March 11, 2025
End Date
September 30, 2028
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Stephanie Baggio

Associate Professor

University of Lausanne

Eligibility Criteria

Inclusion Criteria

  • Vulnerable adolescents defined as being: 1) detained in juvenile detention centers, 2) disconnected from school, 3) in treatment for psychiatric disorders, 4) belonging to a sexual or gender minority, 5) affected by chronic conditions, or 6) with relational/familial problems.
  • Age 14 to 25 years old.
  • Good knowledge of French.
  • Accepting to sign the informed consent.

Exclusion Criteria

  • The medical/educational staff considers that the intervention will interfere with appropriate management of acute psychiatric disorder or may cause harm to self or other.
  • Being enrolled in another suicide prevention intervention during the study period.

Outcomes

Primary Outcomes

Composite measure of suicide awareness

Time Frame: One-week post-baseline

Nine-item perceived suicide awareness scale (PSAS-9), assessed on a 5-point scale, score ranging from 0 to 36, with a higher score indicating a higher suicide awareness

Secondary Outcomes

  • Psychological distress(One-week post-baseline; three-month post-baseline)
  • Composite measure of suicide awareness(Three-month post-baseline)
  • Knowledge on suicide(One-week post-baseline; three-month post-baseline)
  • Knowledge of local resources(One-week post-baseline; three-month post-baseline)
  • Suicidal thoughts(One-week post-baseline; three-month post-baseline)
  • Access to primary suicide prevention(Baseline)
  • Attrition(Three-month post-baseline)

Study Sites (19)

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