Suicide Prevention for Substance Using Youth Experiencing Homelessness

Part of paid clinical trials in Columbus, Ohio.

Sponsor
Ohio State University
Study ID
NCT05994612
Status
Recruiting

Conditions

  • Suicide Prevention

Eligibility Criteria

Sex
ALL
Age
15 Years - 24 Years
Healthy Volunteers
Accepted

Interventions

  • Cognitive Therapy for Suicide Prevention — BEHAVIORAL
    10 sessions of cognitive therapy for suicide prevention plus 9 optional booster sessions
  • Services as Usual — BEHAVIORAL
    Participants will receive services that they would normally receive in the community.

Study Details

Suicide is the leading cause of death among YEH and most youth do not access services that may be available to them. Therefore, this study seeks to address this gap in the research literature with the goal to identify an effective intervention that can be readily adopted by communities that serve these youth. We will test the effects of outreach-worker delivered Cognitive Therapy for Suicide Prevention (CTSP)+Services as Usual (SAU) versus SAU alone on suicidal ideation (primary outcome), substance use and depressive symptoms (secondary outcomes) at 3, 6, 9 and 12- months.

Key Dates

Start date
Nov 20, 2023
Status verified
Apr 2026
Primary completion
Jan 1, 2029
Completion
Jan 1, 2030

Study Design

Enrollment
300 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Experimental: Cognitive Therapy for Suicide Prevention + Services as Usual
    10 sessions of Cognitive Therapy for Suicide Prevention (CTSP) provided over 6 months, with 9 optional booster sessions + services as usual (SAU) received by the community.
  • Active Comparator: Services as Usual
    Services as Usual involves utilizing Strengths-Based Outreach and Advocacy to link youth to community services for a period of 6 months.

Primary Outcome Measure

Suicidal Ideation: Scale for Suicidal Ideation-Worst Point (SSI-W) [ Time Frame: baseline, 3, 6, 9 and 12 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The Ohio State UniversityColumbusOhio43210
Natasha Slesnick, Ph.D.
614-247-8469
Natasha Slesnick, Ph.D. (PRINCIPAL_INVESTIGATOR)

Find similar trials in Columbus, OH

Related Studies