Safety Planning and Cognitive Behavioral Therapy for Adolescent Suicide Prevention in Mozambique

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorUniversity of Washington

About this trial

This implementation research project aims to test the effectiveness and implementation outcomes of suicide safety planning along and a transdiagnostic cognitive behavioral intervention for suicide prevention on decreasing suicidal behaviors in secondary school students in Mozambique. This study will also result in hypothesized mechanisms of intervention effects, costs and cost-effectiveness.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Youth enrolled in a secondary school in Sofala Province that is located within 30 minutes of a health facility that hosts both an urgent care and mental health department.

Youth enrolled in 9th and/or 10th and/or 11th grade.

Legal guardian has provided consent to participate if under 18 or if youth is age 18 or older and has provided consent to participate.

Youth has assented to participation.

Disqualifiers

Youth and/or guardian has not provided consent to participate, or responsible party is unable to provide informed consent.

Youth is not enrolled in a participating secondary school.

Youth declines to assent.

Youth is a ward of the State or any other agency, institution, or entity.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Safety Planning Intervention

    Behavioral

    All behavioral interventions will be provided by a trained nonspecialist healthcare worker, descriptions of each intervention can be found under treatment arm/group descriptions.

  • Enhanced Usual Care

    Behavioral

    All behavioral interventions will be provided by a trained nonspecialist healthcare worker, descriptions of each intervention can be found under treatment arm/group descriptions.

  • Transdiagnostic Cognitive Behavioral Therapy for Suicide Prevention

    Behavioral

    All behavioral interventions will be provided by a trained nonspecialist healthcare worker, descriptions of each intervention can be found under treatment arm/group descriptions.

Treatment groups

2,100 Participants
are divided into 3 treatment groups
Group A: Enhanced Usual CareOther 1 intervention
Group B: Safety Planning InterventionExperimental treatment 1 intervention
Group C: Transdiagnostic Cognitive Behavioral Therapy for Suicide PreventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Suicidal Behavior

As reported on the Columbia Suicide Severity Rating Scale. The responses of the C-SSRS tool are yes or no options that indicate the user's level of risk as low, moderate or high risk of suicide.

Time frame
6-months post intervention

Secondary outcomes

1

Suicidal Behavior - Supplementary analysis of primary outcome

As reported on the Columbia Suicide Severity Rating Scale. The responses of the C-SSRS tool are yes or no options that indicate the user's level of risk as low, moderate or high risk of suicide.

Time frame
3-months post intervention
2

Suicidal Ideation

As reported on the Columbia Suicide Severity Rating Scale. The responses of the C-SSRS tool are yes or no options that indicate the user's level of risk as low, moderate or high risk of suicide.

Time frame
3-, 6-, 12-, and 24-months post intervention
3

Depressive Symptoms

Depressive symptoms as measured on the Patient Health Questionnaire 9 - MZ, the scoring range is 0-27 with higher scores indicative of more severe symptoms

Time frame
3-, 6-, 12-, and 24-months post intervention
4

Suicidal Behavior - Maintenance Indicators

As reported on the Columbia Suicide Severity Rating Scale. The responses of the C-SSRS tool are yes or no options that indicate the user's level of risk as low, moderate or high risk of suicide.

Time frame
12-, and 24-months post intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Washington

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator