90 Participants NeededMy employer runs this trial

YST + CBT-SP for Suicide Risk

Recruiting at 1 trial location
CM
Overseen ByChristina Magness, LMSW
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: University of Michigan
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

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 Is on the Research Team?

CE

Cynthia Ewell Foster, PhD

Principal Investigator

University of Michigan

Are You a Good Fit for This Trial?

Inclusion Criteria

Willing and able to complete enrollment procedures
Willing and able to provide signed and dated informed assent
I can provide at least one contact person for emergencies.
See 12 more

Exclusion Criteria

Participated in the Aim 2a open trial
Do not understand written and spoken English
Actively engaged in specialty mental health treatment
See 5 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive 12-14 sessions of CBT-SP in addition to YST. Support persons attend an education/orientation session and have weekly contact with the youth.

12-14 weeks
Weekly sessions

Follow-up

Participants are monitored for safety and effectiveness after treatment. Assessments occur at baseline, 6 weeks, and 14 weeks.

14 weeks
Assessments at baseline, 6 weeks, and 14 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Cognitive Behavioral Therapy for Suicide Prevention (CBT-SP)
  • Youth-Nominated Support Team (eYST)

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: CBT for Suicide Prevention plus the Youth-Nominated Support TeamExperimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Michigan

Lead Sponsor

Trials
1,891
Recruited
6,458,000+

National Institute of Mental Health (NIMH)

Collaborator

Trials
3,007
Recruited
2,852,000+

MiSide

Collaborator

Children's Hospital of Michigan

Collaborator

Trials
26
Recruited
4,200+