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Building Resilience and Attachment in Vulnerable Adolescents

Brief Group Intervention for Adolescents With Mild to Moderate Suicidal Ideation and Their Caregivers: Preliminary Investigation for a Novel Treatment Approach

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01925807
Acronym
BRAVA
Enrollment
76
Registered
2013-08-20
Start date
2014-02-28
Completion date
2017-05-31
Last updated
2017-08-14

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

Conditions

Suicidal Ideation

Keywords

Adolescent, Suicidal Ideation, Emergency Department, Crisis, Attachment, Coping

Brief summary

Suicide is the second leading cause of mortality for Canadian adolescents. Mental health complaints are one of the leading reasons for an emergency department visit at the Children's Hospital of Eastern Ontario and 60% of adolescents report suicidal ideation. The goal of the present investigation is to test the efficacy of a brief group intervention for adolescents with passive suicidal ideation and their caregivers that will focus on coping, familial support, and emotional regulation. The investigators hypothesize that a brief group intervention, delivered in the weeks following presentation for crisis services, will reduce suicidal ideation and improve coping and familial support.

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. For adolescents, the group sessions will focus on coping strategies and emotional regulation. For caregivers, the group sessions will be focused on attachment, family environment, and validation.

Sponsors

Mach Gaensslen Foundation
CollaboratorOTHER
AFP Innovation Fund
CollaboratorOTHER
Allison Kennedy
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Mild to moderate suicidal ideation * Recently presented for services in response to a psycho-social crisis (Emergency Department, MH Urgent Care) * One or two caregiver(s) committed to attending the majority of sessions

Exclusion criteria

* Presence of a suicidal plan and/or recent gesture/attempt * Psychosis * Schizophrenia * Dual diagnosis * Developmental disability or delay * Behavioural problem as primary concern * Major substance abuse * Currently receiving mental health services (once every two weeks or more frequently) * Inability to commit to majority of sessions (minimum 4 of 6 sessions) * Children's aid society involvement * Inability of at least one caregiver to commit to attending the majority of sessions

Design outcomes

Primary

MeasureTime frameDescription
Suicidal Ideation6 weeksSuicidal ideation will be measured using the Suicidal Ideation Questionnaire Junior (SIQ-JR; Reynolds, 1988). Repeated Measures ANOVA or ANCOVA will be used to compare differences in suicidal ideation within groups (pre-post changes). Further comparisons using clinical cut-off will be conducted via McNemar test for matched pairs.

Secondary

MeasureTime frameDescription
Familial Support6 weeksFamilial support will be measured using questionnaires for both caregivers and youth. Youth will respond to the Family Environment Scale (Koren, DeChillo, & Friesen, 1992) and the Inventory of Parent and Peer Attachment (Armsden & Greenberg, 1987). Caregivers will respond to the Family Environment Scale and and Relationship Scale Questionnaire (Griffine & Gartholomew, 1994). Repeated Measures ANOVA or ANCOVA will be used to compare differences within groups (pre-post changes).

Other

MeasureTime frameDescription
Coping Strategies6 weeksYouth coping strategies will be measured using the Youth Stress and Coping Questionnaire (Cloutier et al., 2008). Repeated Measures ANOVA or ANCOVA will be used to compare differences within groups (pre-post changes).
Depression6 weeksYouth depression will be measured using the Children's Depression Inventory-2 Self report (CDI-2; Kovaks, 2010). Repeated Measures ANOVA or ANCOVA will be used to compare differences within groups (pre-post changes).
Anxiety6 weeksYouth anxiety symptoms will be measured using the Multidimensional Anxiety Scale for Children (MASC-2; March, 1997). Repeated Measures ANOVA or ANCOVA will be used to compare differences within groups (pre-post changes).

Countries

Canada

Outcome results

None listed

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