NCT06353711

Brief Summary

The goal of this pilot randomized control trial (RCT) is to test the feasibility of Caring Connections, a Culturally Adapted Linking Individuals Needing Care (CA-LINC) suicide prevention care coordination intervention for high-risk suicidal youth. This consumer-, community-, and theory-driven care coordination intervention is designed to reduce suicide ideation and behavior (SIB) by improving service engagement. Connections is a 90-day intervention that integrates engagement and follow-up strategies to assess/monitor suicide risk, facilitate service use referrals/linkages, develop/refine safety plans, and create villages of care. The intervention incorporates cultural promotive factors, empowerment, and motivational strategies aimed at supporting youth, enhancing strengths, promoting hope, improving family relationships, and reinforcing caring messages. Primary research questions include: Is Caring Connections feasible to use for suicidal high-risk youth? Does Caring Connections have the potential to reduce suicide ideation and behaviors among high-risk suicidal youth? For the pilot RCT, 80 youth participants ages 13-19 who meet the inclusion criteria will be randomly assigned to one of two conditions: Caring Connections (n=40) or Treatment as Usual (n=40). Additionally, investigators will enroll 80 caregivers of youth meeting inclusion criteria and 20 Mental Healthcare, Healthcare Providers, Community Stakeholders, and/or Care Coordinators with experience working with suicidal youth. Researchers will compare those receiving Caring Connections with treatment as usual to see if suicidal ideation and behaviors, and engagement.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
4mo left

Started Aug 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress74%
Aug 2025Oct 2026

First Submitted

Initial submission to the registry

April 2, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 9, 2024

Completed
1.3 years until next milestone

Study Start

First participant enrolled

August 14, 2025

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

March 17, 2026

Status Verified

March 1, 2026

Enrollment Period

1.1 years

First QC Date

April 2, 2024

Last Update Submit

March 13, 2026

Conditions

Keywords

Black youthsuicideideationattempts

Outcome Measures

Primary Outcomes (2)

  • Change in Suicide Ideation Severity

    Investigators assess the suicide ideation severity using the Columbia-Suicide Severity Rating Scale (C-SSRS), a 6-item validated tool used to assess a person's risk for suicide. Assess suicidal ideation severity (5 items \[yes/no\]; scores range from 0 to 5, with higher scores indicating more severe suicidal ideation)

    Baseline, 30 days, 90 days, 180 days

  • Reported Suicide Attempts

    Investigators will assess the presence of suicidal behaviors (yes/no) over the past month. Question #6 from the Columbia-Suicide Severity Rating Scale (C-SSRS) will be used, which assesses a person's risk for suicide. A yes response indicates suicidal behaviors.

    Baseline, 30 days, 90 days, 180 days

Other Outcomes (5)

  • Change in Treatment Acceptability

    30 days, 90 days

  • Change in Therapeutic Alliance

    30 days, 90 days

  • Change in Cultural Humility

    30 days, 90 days

  • +2 more other outcomes

Study Arms (2)

Caring Connections

EXPERIMENTAL

Caring Connections is a 90-day culturally adapted LINC intervention developed with and for youth. The Caring Connection intervention integrates engagement and follow-up strategies to assess/monitor suicide risk, facilitate service use referrals/linkages, develop/refine safety plans, and create villages of care. The Caring Connections intervention incorporates culturally promotive factors, empowerment, and motivational strategies to support, enhance strengths, promote hope, improve family relationships, and reinforce caring messages. This consumer-, community-, and theory-driven care coordination intervention is designed to reduce suicide ideation and behavior (SIB) by improving service engagement and delivery standards. Caring Connections is implemented by Peer Support Specialists and Community Health Workers assigned to mental health "hubs" in Faith-Based Organizations (FBOs) to facilitate standardization and access to care.

Behavioral: Caring Connections

Treatment as Usual

ACTIVE COMPARATOR

The treatment-as-usual arm includes care coordination services provided by Peer Support Specialists and Community Health Workers in the faith-based organization mental health hubs. This condition includes screening to determine youth suicide risk (high vs. low). Youth presenting with high risk are typically referred to an inpatient treatment facility. Youth presenting with low risk may be referred to a local outpatient provider. Mental health hub staff may attempt to follow up with families (typically not more than a one-time check-in) to ensure they are connected to the referral source. Following initial referrals, mental health hubs typically continue to provide crisis response and referral services to youth and caregivers as needed.

Behavioral: Treatment as Usual

Interventions

Participants received the Caring Connections Intervention.

Caring Connections

Participants received Treatment as Usual

Treatment as Usual

Eligibility Criteria

Age13 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Youth:
  • years old
  • Current or recent history (\<90 days) of suicide ideation, planning, or attempts or nonsuicidal self-injurious behaviors per youth or caregiver self-report or positive screen on the Patient Health Questionnaire Adolescent (PHQ-A), C-SSRS, or Ask Suicide-Screening Questions (ASQ).
  • Able to fluently speak and read English
  • Youth with a prior history of difficulty accessing services.
  • Written assent to participate in the study (\<18 years old)
  • Written consent from a parent/legal guardian/caregiver to participate in the study (\<18 years old)
  • Written consent if the youth is ages 18-19
  • Parents/Legal Guardians/Caregivers:
  • Over the age of 18
  • Able to fluently speak and read English
  • Without intellectual disabilities
  • Provide written consent to participate
  • Mental Healthcare and/or Healthcare Providers and/or Community Stakeholders:
  • Mental Health, behavioral health, substance use and/or health-related professionals who screen/assess for mental health and/or suicide risk or provide referrals, treatment, or follow-up care to youth with a prior history of difficulty accessing services in the surrounding treatment areas based on this risk or community stakeholder (i.e., faith-based leaders, agency directors, advocates, school administrators, hospital/crisis directors, topical experts, etc.).
  • +9 more criteria

You may not qualify if:

  • Youth:
  • Youth at imminent suicide risk (reported verbally and/or indicated on C-SSRS)
  • Youth who exhibit severe cognitive, language, or developmental delays
  • Parents/Legal Guardians/Caregivers:
  • Mental Healthcare and/or Healthcare Providers and/or Community Stakeholders:

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The University of North Carolina at Charlotte

Charlotte, North Carolina, 28223, United States

RECRUITING

Related Publications (5)

  • Richardson SC, Phipps-Bennett M, Gryglewicz K, Vance M, Williams JA, Bey I, Herbert R, Dennis S, Karver MS. Making deep-structure adaptations: A community-engaged qualitative study for culturally adapting suicide prevention interventions for Black youth. Cultur Divers Ethnic Minor Psychol. 2025 Sep 1:10.1037/cdp0000770. doi: 10.1037/cdp0000770. Online ahead of print.

    PMID: 40892589BACKGROUND
  • Richardson SC, Gryglewicz K, Williams JA, Phipps-Bennett M, Dennis S, Browne N, Trujillo A, Carlisle C, Nail M, Karver M. The Pursuit of Radical Hope: Suicidal Help-Seeking Behaviors Among Black Adolescents and Caregivers. J Clin Child Adolesc Psychol. 2025 Nov 20:1-15. doi: 10.1080/15374416.2025.2579278. Online ahead of print.

    PMID: 41264369BACKGROUND
  • Vance MM, Gryglewicz K, Nam E, Richardson S, Borntrager L, Karver MS. Exploring Service Use Disparities among Suicidal Black Youth in a Suicide Prevention Care Coordination Intervention. J Racial Ethn Health Disparities. 2023 Oct;10(5):2231-2243. doi: 10.1007/s40615-022-01402-7. Epub 2022 Sep 13.

    PMID: 36100810BACKGROUND
  • Gryglewicz K, Peterson A, Nam E, Vance MM, Borntrager L, Karver MS. Caring Transitions - A Care Coordination Intervention to Reduce Suicide Risk Among Youth Discharged From Inpatient Psychiatric Hospitalization. Crisis. 2023 Jan;44(1):7-13. doi: 10.1027/0227-5910/a000795. Epub 2021 Jun 15.

    PMID: 34128700BACKGROUND
  • Richardson SC, Gunn LH, Phipps M, Azasu E. Factors Associated with Suicide Risk Behavior Outcomes Among Black High School Adolescents. J Community Health. 2024 Jun;49(3):466-474. doi: 10.1007/s10900-023-01312-7. Epub 2023 Dec 14.

    PMID: 38095815BACKGROUND

MeSH Terms

Conditions

SuicideSuicide PreventionSuicide, Attempted

Interventions

Therapeutics

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Sonyia C Richardson, Ph.D.

    University of North Carolina, Chapel Hill

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sonyia C Richardson, Ph.D.

CONTACT

Margaret Phipps-Bennett, M.S.W.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 2, 2024

First Posted

April 9, 2024

Study Start

August 14, 2025

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 1, 2026

Last Updated

March 17, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will share

Deidentified individual data that supports the results will be shared beginning 9 to 36 months following publication, provided the investigator who proposes to use the data has approval from an Institutional Review Board (IRB), Independent Ethics Committee (IEC), or Research Ethics Board (REB), as applicable, and executes a data use/sharing agreement with UNC.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
The data will become available beginning 9 to 36 months following publication.
Access Criteria
See the Plan Description section above for IRB or similar authorization prior to access. Once those criteria have been met, an interested investigator may contact the study PI by email (sonyia.richardson@unc.edu); the PI would arrange for deidentified data sharing in accordance with university policy.

Locations