NCT07506460 Integrating the Youth Nominated Support Team (YST) With CBT for Black Youth With Acute Suicide Risk: Aim 2b
| NCT ID | NCT07506460 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Michigan |
| Condition | Suicide Prevention |
| Study Type | INTERVENTIONAL |
| Enrollment | 90 participants |
| Start Date | 2026-03-23 |
| Primary Completion | 2026-08 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 90 participants in total. It began in 2026-03-23 with a primary completion date of 2026-08.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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.
Eligibility Criteria
Youth Inclusion Criteria: * Patients that are able to provide at least one verifiable contact for emergency or tracking purposes * Willing to receive care at MiSide * Present to an acute emergency care setting with suicide risk (per protocol) * Self-identify as Black * Willing and able to complete enrollment procedures * Willing and able to provide signed and dated informed assent Youth Exclusion Criteria: * Unable to be consented in English * Do not have a parent/legal guardian available to provide consent * Are not able to provide informed assent or to participate in the assessment due to significant agitation, psychosis, cognitive impairment, learning disability, or medical trauma * Actively engaged in specialty mental health treatment * Participated in the Aim 2a open trial Parent/Guardian Inclusion Criteria: * Adults 18 years and older * The parent or legal guardian of a youth participating in this Aim * Understand written and spoken English * Willing and able to complete enrollment procedures * Willing and able to provide signed and dated informed consent * Need to have access to technology, either cell or an email address Parent/Guardian Exclusion Criteria: \- Do not understand written and spoken English Support Person Inclusion Criteria: * Adults 18 years and older * Understand written and spoken English * Approved to serve as a support person by the parent/legal guardian Support Person Exclusion Criteria: * Do not understand written and spoken English * Not approved to serve as a support person by the parent/guardian
Contact & Investigator
Cynthia Ewell Foster, PhD
PRINCIPAL INVESTIGATOR
University of Michigan
Frequently Asked Questions
Who can join the NCT07506460 clinical trial?
This trial is open to participants of all sexes, aged 12 Years or older, studying Suicide Prevention. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07506460 currently recruiting?
Yes, NCT07506460 is actively recruiting participants. Contact the research team at cmagness@med.umich.edu for enrollment information.
Where is the NCT07506460 trial being conducted?
This trial is being conducted at Detroit, United States, Detroit, United States.
Who is sponsoring the NCT07506460 clinical trial?
NCT07506460 is sponsored by University of Michigan. The principal investigator is Cynthia Ewell Foster, PhD at University of Michigan. The trial plans to enroll 90 participants.