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Bridge the Gap (BTG) - Black Youth Group

Bridging the Gap: A Collaborative Intervention Group for Black Youth at Risk for Suicide

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06880809
Acronym
Bridge the Gap
Enrollment
16
Registered
2025-03-18
Start date
2025-06-01
Completion date
2027-06-01
Last updated
2026-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide Prevention

Keywords

Suicide Prevention, Black Youth, Collaborative Assessment & Management of Suicidality (CAMS), Group Intervention

Brief summary

The goal of this clinical trial is to develop and preliminarily test a culturally adapted suicide intervention specifically for black youth. The main question it aims to answer: -To evaluate the feasibility and acceptability of the group, as well as the preliminary efficacy of the group for decreasing suicidal thoughts and behaviors and increasing protective factors such as hope, positive ethnic identity, and family and peer support. Participants will be asked to attend 10-week group intervention and complete pre-treatment and post-treatment assessment measures.

Interventions

BEHAVIORALBridge the Gap (BTG) - Black Youth Group

Participants will complete a group intervention, rooted in the Collaborative Assessment \& Management of Suicidality (CAMS) evidence-based model, driven by their own unique identification of suicide drivers.

Sponsors

Children's Hospital Los Angeles
Lead SponsorOTHER
American Psychological Foundation
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
Yes

Inclusion criteria

* 12-17 years old * Identify as Black or African American or being of African descent * Have current suicidal ideation or suicidal ideation within the last 30 days * Have assent from the adolescent participant and consent from an individual's caregiver or guardian to participate.

Exclusion criteria

* An active psychotic disorder or current psychosis symptoms * No history of suicide attempt(s) or suicide ideation in the past 30 days * Cognitive deficits or a medical condition diagnosed from a medical provider that precludes full understanding of study materials as assessed through an inability to complete the pre-treatment CAMS SSF \& SSP * Caregivers, guardians, and/or the patient refuse to participate.

Design outcomes

Primary

MeasureTime frameDescription
The Collaborative Assessment & Management of Suicidality - Suicide Status Form (SSF)From pre-treatment until 3 months post-treatment, approximately 23 weeks.An assessment of suicide risk that consists of six core assessment constructs: psychological pain, stress, agitation, hopelessness, self-hate, and overall risk of suicide; as well as reasons for living and reasons for dying constructs, and wish to live and wish to die constructs.
Ethnic Identity Scale (EIS)From baseline until 3 months post-treatment, approximately 22 weeks.A 17-item scale that assesses the three components of ethnic identity and distinguishes between exploration, resolution, and affirmation. Scores range from 17-68, with higher scores indicating higher levels of affirmation, exploration, and resolution.
Living Ladder ScaleFrom baseline until 3 months post-treatment, approximately 22 weeks.A one-item measure that is prospectively associated with suicidal ideation and suicide attempts by measuring readiness to continue living among individuals thinking of suicide. Scores range from 0-8, with 8 indicating an individual is committed to making changes to make their lives worth living.
Brief Suicide Cognitions Scale (B-SCS)From baseline until 3 months post-treatment, approximately 22 weeks.A 6-item self-report scale that measures the suicidal belief system, including dimensions of unlovability, unbearability, and unsolvability. Scores range from 6-30, with lower scores indicating fewer suicide cognitions.
Therapeutic Relationship Working Alliance Inventory, Short Revised (WAI-SR)From baseline until 3 months post-treatment, approximately 22 weeks.A 12-item scale that reflects Bordin's three-dimensional conceptualization of therapeutic alliance: task, goal, and bond. Scores range from 12-60, with higher scores indicating higher therapeutic alliance.
Optimism and Hope Scale (OHS)From baseline until 3 months post-treatment, approximately 22 weeks.A 14-item scale that measures an individual's level of both optimism, as characterized by a positive outlook on the future, and hope, as characterized by the belief in one's ability to achieve goals and navigate challenges. Scores range from 14-56, with lower scores indicating more hope and optimism.
Parent Readiness for Hospital Discharge Scale (RHDS)From baseline until 3 months post-treatment, approximately 22 weeks.A 23-item scale aimed at providing a discharge readiness assessment before pediatric discharge from care in hospital settings. Scores range from 0-80, with higher scores indicating more readiness.
Group Cohesion ScaleFrom baseline until the beginning of post-treatment, approximately 10 weeks.A 12-item self-report scale that measures group cohesion, including dimensions of engagement, conflict, and avoidance. Scores across the subscales range from 0-72; higher scores indicate more of that dimension.

Countries

United States

Contacts

CONTACTTia Tyndal, PhD
ttyndal@chla.usc.edu323-361-4648
CONTACTAmy West, PhD
amwest@chla.usc.edu323-361-4478
PRINCIPAL_INVESTIGATORTia Tyndal, PhD

Children's Hospital Los Angeles

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 1, 2026