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BRAVA: Building Resilience and Attachment in Vulnerable Adolescents

Building Resilience and Attachment in Vulnerable Adolescents (BRAVA): A Randomized Controlled Trial of a Brief Group Intervention for Adolescents With Mild to Moderate Suicidal Ideation and Their Caregivers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04751968
Acronym
BRAVA
Enrollment
99
Registered
2021-02-12
Start date
2021-04-12
Completion date
2023-08-25
Last updated
2024-05-06

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

Conditions

Suicidal Ideation, Suicide and Self-harm

Keywords

Adolescent, Suicidal ideation, Group therapy, Crisis

Brief summary

The prevalence of suicidal ideation (SI) among adolescents in North America is high, making it critical to develop evidence-based brief interventions for adolescents with SI that target healthy coping skills and relationships. BRAVA is a novel brief group intervention for adolescents with mild to moderate SI and their caregivers; youth are taught skills for coping and relating more effectively with others. Caregivers learn about adolescent development, effective parenting and the importance of connection. The goal of the randomized controlled trial is to assess the efficacy of a virtually-delivered, brief group intervention for adolescents with mild to moderate SI and their caregivers in reducing SI.

Interventions

The intervention will consist of 6 psycho-educational group sessions for caregivers and 6 psycho-educational group sessions for adolescents. Adolescent and caregiver sessions will be held separately and will focus on different issues. Adolescents are taught skills for coping and relating more effectively with others. Caregivers learn about adolescent development, effective parenting and the importance of connection. The groups consist of 6 stand-alone modules permitting rolling entry and prompt access. Youth and Caregivers will receive a weekly text message reminder of their exit assessment date/time, homework from that week's intervention group and crisis resources.

BEHAVIORALEnhanced Treatment as Usual

Youth and Caregivers will receive a weekly text message reminder of their exit assessment date/time, a mental health tip and crisis resources.

Sponsors

Mach Gaensslen Foundation
CollaboratorOTHER
Children's Hospital of Eastern Ontario Research Institute
CollaboratorOTHER
Children's Hospital of Eastern Ontario
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Adolescents 13 years old to 17.5 years old * Mild to moderate suicidal ideation (SI without plan or gesture; 1 on the HEADS-ED) (Cappelli, et al., 2012) * Interested in study participation * Access to an electronic device with internet and email capabilities, and a functioning camera and microphone

Exclusion criteria

* SI with plan or gesture (2 on HEADS ED; indicated plan or gesture) * Comorbid disorders (psychosis, schizophrenia, developmental disabilities, major substance abuse, and severe eating disorders). * Referring clinician has identified an externalizing disorder as a primary diagnosis or primary concern (e.g. Conduct Disorder) * Currently participating in regular psychotherapy at least one time per week * Currently under Children's Aid Society care * Currently in the CHEO ED on a Form 1 or Form 2, or placed on a Section 17. * Express difficulty with reading and writing

Design outcomes

Primary

MeasureTime frameDescription
Suicidal Ideation6 weeksSuicidal ideation will be measured using the Suicidal Ideation Questionnaire Junior (Reynolds, 1988). A decreased score in suicidal ideation over 6-weeks will indicate a positive outcome.

Secondary

MeasureTime frameDescription
Depression and Anxiety6 weeksWe will be assessing youth depression and anxiety with the youth version of the Revised Child Anxiety and Depression Scale (Chorpita et al., 2000). A decreased score in depression and anxiety over 6-weeks will indicate a positive outcome.
Attachment6 weeksWe will be assessing caregiver attachment with the adolescent version of the Adolescent Attachment Anxiety & Avoidance Inventory (Morretti & Obsuth, 2009). A decreased score in attachment between the adolescent and caregiver over 6-weeks will indicate a positive outcome.
Family Functioning6 weeksFamily functioning using the Family Assessment Device (Epstein, Baldwin, & Bishop, 1983). A decreased score in family functioning over 6-weeks will indicate a positive outcome.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026