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Randomized Controlled Trial of the Effectiveness of Group Treatment With War-Exposed Bosnian Adolescents

Long-Term Post- War Adjustment in Bosnian Adolescents, Their Parents and Teachers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00480480
Enrollment
144
Registered
2007-05-31
Start date
2000-09-30
Completion date
2001-10-31
Last updated
2007-05-31

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

Conditions

Depression, Grief (Traumatic Grief and Existential Grief), Posttraumatic Stress Disorder

Keywords

Trauma, Grief, Depression, Adolescent, War, Group, Therapy, Treatment, Intervention, School, Development

Brief summary

Context: This is the first multi-site randomized controlled study of the effectiveness of a group treatment for war-exposed adolescents delivered in-country within a public school system. Objective: To evaluate the effectiveness of a trauma/grief-focused group treatment program in reducing symptoms of posttraumatic stress disorder (PTSD), depression, and traumatic grief in war-exposed Bosnian youths attending 10 secondary schools located in Central Bosnia.

Detailed description

Design: A randomized controlled trial conducted during the 2000-2001 school year, with 4-month follow-up, compared group treatment to a psychoeducation/skill-based school milieu intervention. Setting and Participants: Students attending 10 Bosnian secondary schools exposed to severe trauma, traumatic loss, and severe adversity, reporting severe persisting symptoms of PTSD, depression, or traumatic grief, and functional impairment. Intervention: Students were randomly assigned to either 17-session Trauma and Grief Component Therapy (n=71), or a school milieu intervention (n=73), both conducted by trained school counselors.

Interventions

BEHAVIORALTrauma and Grief Component Therapy for Adolescents (Group Version)

Sponsors

UNICEF
CollaboratorOTHER
Brigham Young University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
14 Years to 19 Years
Healthy volunteers
Yes

Inclusion criteria

* Significant trauma exposure before, during, or after the war (e.g., serious physical injury, life threat, witnessing death or serious injury, traumatic bereavement); * Significant current distress, especially severe persisting symptoms of PTSD, depression, or traumatic grief; * Significant functional impairment in family or peer relationships and school performance

Exclusion criteria

* Acute risk status (e.g., suicidal plans and intent) * Psychosis * Severe substance abuse (severe enough to interfere with engagement in treatment).

Design outcomes

Primary

MeasureTime frame
UCLA PTSD Reaction IndexPre-treatment, post-treatment, and at 4-month follow-up
Depression Self-Rating ScalePre-treatment, post-treatment, and 4-month follow-up
UCLA Grief ScalePre-treatment, post-treatment

Secondary

MeasureTime frame
Trauma Reminder Screening ScalePre-treatment (screening survey)
Cognitive Distortions ScalePre-treatment and post-treatment
Youth Outcome Questionnaire (Somatic and Interpersonal Problems Subscales)Pre- and post-treatment
Loss Reminder Screening ScalePre-treatment (screening survey)
War Exposure IndexPre-treatment (screening survey)
Post-War Adversities ScalePre-treatment (screening survey)

Outcome results

None listed

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