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Recruiting NCT07125144

Piloting a Culturally Adapted Suicide Prevention for Black Students in Chicago

No phase Interventional Suicide Suicidal Ideation Suicide Attempt

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Black Youth Suicide Prevention in Chicago, Signs of Suicide: Standard/Existing.
Who it may be relevant to
Registry conditions: Suicide, Suicidal Ideation, Suicide Attempt. Basic parameters: 11 years — 15 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Piloting a Culturally Adapted Multilevel Suicide Prevention Intervention in Schools for Black Youth and Their Families

Overview

Suicide has been the third leading cause of death for Black youth in the U.S since the 1980s and persists as a leading cause of death for Black youth today. For example, in 2018 suicide was reported as the 2nd leading cause of death among Black Americans ages 10 to14 years old. Findings yielded from recent queries indicate that the gap in suicides among Black males and female youth has narrowed in recent years. Despite these disturbing trends, a dearth persists in our understanding of the factors that contribute to and prevent against suicide in Black youth, thus diminishing researchers' ability to effectively detect suicide risk in this particular population. This project aims to redress this gap by proposing the cultural adaptation of an existing suicide prevention intervention, the Signs of Suicide (SOS) prevention program, for Black middle school students. Our team will conduct a pilot randomized controlled trial among a sample of Black middle school students to assess feasibility and examine underlying mechanisms that contribute to suicidality among Black youth. Intervention content will be adapted to assess how topics of racial identity, racial socialization, and racial discrimination uniquely impact Black youth's mental health experiences and risk for suicide. Measures of suicidal ideation, planning, and attempt will be assessed at pre-test, post-test, and 3-months after the intervention. Findings derived from this project will contribute to public health priorities by offering unique insight into the factors that either prevent or promote suicide among Black youth and could be replicated in other schools serving Black students across the nation.

Interventions

  • Behavioral Black Youth Suicide Prevention in Chicago
    The Culturally Adapted intervention uses intervention video content that specifically addresses topics that shape Black youth's psychological wellbeing and development. The goal of this intervention is to share suicide prevention information in ways that are culturally responsive and attentive to the specific needs of Black adolescents.
  • Behavioral Signs of Suicide: Standard/Existing
    Students attending schools assigned to the Standard/Existing Intervention condition will receive the Signs of Suicide curriculum.

Primary outcome measures

  • Suicidal Ideation [Time frame: Baseline, 2 weeks after baseline, 3-months after baseline]
Secondary outcome measures (3)
  • Suicide Attempt [Time frame: Baseline, 2 weeks after baseline, 3-months after baseline]
  • Knowledge of Depression and Suicide [Time frame: Baseline, 2 weeks after baseline, 3-months after baseline]
  • Attitudes Towards Depression and Suicide [Time frame: Baseline, 2 weeks after baseline, 3-months after baseline]

Eligibility criteria

Inclusion criteria

  • Enrolled in 6th, 7th, or 8th grade at a participating school

Exclusion criteria

  • Not enrolled in 6th, 7th, or 8th grade at a participating school

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

United States · 1 center
  • University of Chicago — Chicago

Identifiers

NCT: NCT07125144 · R34MH129789 · R34MH129789

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗