Evaluating Primary Suicide Prevention in Adolescents With Risk Factors
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.
Investigators
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)