Culturally adapted suicide prevention for Black middle school students in Chicago

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The project adapts the existing Signs of Suicide (SOS) program to better reflect the cultural context of Black middle school students and their communities. Investigators will run a pilot randomized controlled trial in Chicago middle schools, enrolling Black students in grades 6–8 and comparing the culturally adapted SOS to the standard SOS program. The study will measure feasibility and acceptability of the adapted program and collect initial data on suicide-related knowledge, help-seeking behavior, and self-reported suicidal thoughts or attempts. Results will guide whether a larger effectiveness trial and broader implementation are warranted.

Why it matters

Who can join: the full rules

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

Where it's running

• University of Chicago
  Chicago, Illinois, United States Recruiting

Study contacts

• Principal investigator: Janelle R. Goodwill, PhD — University of Chicago
• Study coordinator: Janelle R Goodwill, PhD
• Email: jgoodwill@uchicago.edu
• Phone: 773-834-5114

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Attempted Suicide Short Intervention Program for Older Adults (ASSIP-OA) for people aged 65 and up

  This randomized study will test whether a version of the ASSIP counseling program adapted for people aged 65 and older reduces repeat suicide attempts and ongoing suicidal thoughts compared with usual care.

  Recruiting Vastra Gotaland Region · Borås and 1 other locations · NCT06831942

• Inhaled DMT for major depressive disorder

  This trial tests whether inhaled DMT can quickly ease depressive symptoms and reduce suicide risk in adults with major depressive disorder.

  Recruiting Phase 2 Universidade Federal do Rio Grande do Norte · Fortaleza, Ceará and 4 other locations · NCT07562191

• Remote case management to prevent suicide after psychiatric hospital discharge

  This project will test whether a 6-month remote program called Pathfinding helps active-duty Army soldiers reduce suicidal behavior after leaving inpatient psychiatric care.

  Recruiting Uniformed Services University of the Health Sciences · Bethesda, Maryland · NCT07404787

• Text reminders to help parents keep teens safe after a suicide-related ED visit

  This study tests whether sending parents text messages can help them reduce their teen’s access to lethal means and increase safety practices after a suicide-related emergency visit.

  Recruiting University of Texas Southwestern Medical Center · Dallas, Texas · NCT07383714

• Co-creating suicide prevention tools for people in prison

  This project will work with people in prison and prison care staff to test and adapt three suicide prevention tools so they fit prison life and are easier to use.

  Recruiting University Ghent · Ghent, East-Flanders · NCT07259408

• Crisis Response Planning added to intensive Cognitive Processing Therapy to reduce suicide risk in PTSD

  We will test whether adding Crisis Response Planning to intensive Cognitive Processing Therapy helps reduce suicidal thoughts and behaviors in military members and veterans with PTSD.

  Recruiting Ohio State University · Fort Hood, Texas · NCT07238192

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.