Bridge the Gap (BTG) - Black Youth Group

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age12-17
SponsorChildren's Hospital Los Angeles

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Single group

Treatments tested in this trial

  • Bridge the Gap (BTG) - Black Youth Group

    Behavioral

    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.

Treatment groups

16 Participants
are divided into 1 treatment group
Group A: Treatment ArmExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The Collaborative Assessment & Management of Suicidality - Suicide Status Form (SSF)

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.

Time frame
From pre-treatment until 3 months post-treatment, approximately 23 weeks.
2

Ethnic Identity Scale (EIS)

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.

Time frame
From baseline until 3 months post-treatment, approximately 22 weeks.
3

Living Ladder Scale

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.

Time frame
From baseline until 3 months post-treatment, approximately 22 weeks.
4

Brief Suicide Cognitions Scale (B-SCS)

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.

Time frame
From baseline until 3 months post-treatment, approximately 22 weeks.

Secondary outcomes

Other outcomes

Sponsors and contacts

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Children's Hospital Los Angeles

Lead sponsor

American Psychological Foundation

Collaborator