Caring Connections Youth Suicide Prevention Randomized Control Trial
A Culturally Adapted Care Coordination Intervention for High-Risk Suicidal Youth
Led by University of North Carolina, Chapel Hill · Updated on 2026-03-17
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AI-Summary
Brief Title
Who Can Participate
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Your Study Journey
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Sponsors
U
University of North Carolina, Chapel Hill
Lead Sponsor
N
National Institute of Mental Health (NIMH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating Caring Connections, a culturally adapted care coordination intervention designed for high-risk suicidal youth aged 13 to 19. This pilot randomized control trial aims to test the feasibility of Caring Connections to reduce suicidal thoughts and behaviors by improving engagement with mental health services. The study also compares Caring Connections to Treatment as Usual to assess differences in suicide ideation, behaviors, and engagement among youth. The intervention incorporates community and cultural input, empowerment, motivational strategies, and family relationship support to promote hope and strength.
The study involves two groups: one receiving Caring Connections and the other receiving Treatment as Usual. Caring Connections is a 90-day intervention delivered by Peer Support Specialists and Community Health Workers based in mental health hubs within Faith-Based Organizations. It includes ongoing suicide risk monitoring, service referrals, safety plan development, and building supportive care networks. Treatment as Usual includes standard care coordination with crisis response and referral services, typically involving risk screening and one-time follow-up. Both interventions aim to connect youth and families to appropriate resources.
Participants include youth with recent suicidal ideation or behaviors, their caregivers, and relevant healthcare providers or community stakeholders. Data collection occurs at baseline, 30, 90, and 180 days, with evaluations conducted by blinded research assistants. The trial measures changes in suicide ideation severity and reported suicide attempts over time. Researchers will also assess the acceptability, practicality, integration, treatment adherence, fidelity, and retention related to Caring Connections. The study runs through October 2026 and includes follow-up to evaluate service engagement and suicide risk reduction.
CONDITIONS
Brief Title
Caring Connections Youth Suicide Detection and Intervention Study
Who Can Participate
Age: 13Years +
All Genders
Eligibility Criteria
You may qualify if you...
Youth aged 13 to 19 years
Current or recent history (less than 90 days) of suicidal thoughts, planning, attempts, or nonsuicidal self-injurious behaviors
Able to fluently speak and read English
Youth with prior difficulty accessing services
Written assent from youth under 18 years
Written consent from parent/legal guardian for youth under 18 years
Written consent from youth aged 18 to 19 years
Primary caregivers of eligible youth, over 18 years old, fluent in English, without intellectual disabilities, and providing consent
Mental healthcare providers, healthcare professionals, community stakeholders, or care coordinators over 18 years old, fluent in English, without intellectual disabilities, and providing consent
You will not qualify if you...
Youth at imminent suicide risk as indicated verbally or on suicide risk screening
Youth with severe cognitive, language, or developmental delays
Youth not meeting inclusion criteria
Caregivers not meeting inclusion criteria
Mental healthcare providers or community stakeholders not meeting inclusion criteria
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
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Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Outpatient Treatment
Duration - 90 days
Participants receive either the Caring Connections intervention or Treatment as Usual, which includes care coordination services provided by Peer Support Specialists and Community Health Workers in faith-based organization mental health hubs. The intervention aims to reduce suicide ideation and behaviors by improving service engagement and delivery standards with culturally adapted strategies.
Measures/data collection at baseline, 30, 90, and 180 days
Follow-up
Duration - Up to 180 days post-baseline
Participants are monitored after the treatment period to assess changes in suicide ideation severity and reported suicide attempts, supporting evaluation of intervention impact over time.