Actively Recruiting

Phase Not Applicable
Age: 13Years +
All Genders
ID06353711

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

180

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

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

Eligible

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
Not Eligible

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

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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.

Measures collected at 180 days

Trial Site Locations

Total: 1 location

1

The University of North Carolina at Charlotte

Charlotte, North Carolina, United States, 28223

Actively Recruiting

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Research Team

S

Sonyia C Richardson, Ph.D.

M

Margaret Phipps-Bennett, M.S.W.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Published Research Related To This Trial

Making deep-structure adaptations: A community-engaged qualitative study for culturally adapting suicide prevention interventions for Black youth.

Sonyia C Richardson, Margaret Phipps-Bennett, Kim Gryglewicz...

https://pubmed.ncbi.nlm.nih.gov/40892589

The Pursuit of Radical Hope: Suicidal Help-Seeking Behaviors Among Black Adolescents and Caregivers.

Sonyia C Richardson, Kimberly Gryglewicz, John A Williams...

https://pubmed.ncbi.nlm.nih.gov/41264369

Exploring Service Use Disparities among Suicidal Black Youth in a Suicide Prevention Care Coordination Intervention.

Michelle M Vance, Kim Gryglewicz, Eunji Nam...

https://pubmed.ncbi.nlm.nih.gov/36100810

Caring Transitions - A Care Coordination Intervention to Reduce Suicide Risk Among Youth Discharged From Inpatient Psychiatric Hospitalization.

Kim Gryglewicz, Amanda Peterson, Eunji Nam...

https://pubmed.ncbi.nlm.nih.gov/34128700