Integrating the Youth Nominated Support Team (YST) With CBT for Black Youth With Acute Suicide Risk: Aim 2b (NCT07506460)
Integrating the Youth Nominated Support Team (YST) With CBT for Black Youth With Acute Suicide Risk
🩺 Plain-English Summary (8th-Grade Level)
This is a second pilot study being completed based on lessons learned from the Aim 2a feasibility pilot study (NCT06941311). Following modifications, the investigators are testing the acceptability, feasibility, and preliminary effectiveness of the combination of two psychosocial interventions, Cognitive Behavioral Therapy for Suicide Prevention (CBT-SP) and the computer-assisted version of the Youth-Nominated Support Team (eYST). In this phase of the study, CBT-SP + eYST will be tested in an open trial (number of youth = 15). Investigators will recruit Black adolescents (ages 12-17) that come to an urban acute care setting for suicidal thoughts and/or self-injurious behaviors to receive the intervention in an outpatient community mental health agency. Participants will receive 12-14 sessions of CBT-SP in addition to YST. Participants will nominate up to 5 caring adults in their lives to serve as support persons. These support persons will attend an education/orientation session to learn more about their role and how to support the youth. Support persons will have weekly contact with the youth and weekly follow up contacts from the youth's clinician/YST intervention specialist. Youth will be assessed at baseline, 6 weeks, and 14 weeks. Parents will be assessed at baseline and 14 weeks. Support persons will be assessed at baseline and 14 weeks. Fidelity assessments will be completed by clinicians after each session, after the YST psycho-ed session, and weekly to document contact with the support team.
Who can join: Review the eligibility criteria below.
Location: Children's Hospital of Michigan (CHM) Emergency Department — Detroit, Michigan
Age range: 12 Years
🧪 Interventions in This Study
- Cognitive Behavioral Therapy for Suicide Prevention (CBT-SP) (BEHAVIORAL)
- Youth-Nominated Support Team (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (2 Sites)
- Children's Hospital of Michigan (CHM) Emergency Department — Detroit, Michigan
- MiSide — Detroit, Michigan
📞 Contact the Study Coordinator
Phone: (734) 252-6315
Email: cmagness@med.umich.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Suicide Prevention
- Efficacy-Implementation Study for PC CARES in Rural Alaska — Fairbanks, Alaska
- Randomized Controlled Effectiveness Trial of VA S.A.V.E. — Portland, Oregon
- Developing and Piloting an Implementation Strategy for a Brief, Motivational Interviewing-based Lethal Means Safety Counseling Intervention in Primary Care Settings — West Haven, Connecticut
- Retreat-Based Program for Violence-Exposed Women Veterans — West Haven, Connecticut
- Caring Contacts Via Text Message for Suicidal Adolescents After Emergency Department Discharge — Chicago, Illinois
- Suicide Safety Planning — Pleasanton, California
Explore by condition: All Suicide Prevention clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.