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Preventing Youth Suicide in Primary Care: A Family Model

Preventing Youth Suicide in Primary Care: A Family Model

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00604097
Enrollment
66
Registered
2008-01-29
Start date
2004-09-30
Completion date
2008-08-31
Last updated
2012-12-17

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

Conditions

Suicide

Keywords

youth suicide, family therapy, primary care, intervention

Brief summary

The purpose of the study is to test the efficacy of a brief family therapy (Attachment-Based Family Therapy) for youth presenting in primary care with suicidal ideation and depressed mood.

Detailed description

Youth suicide is a serious public health problem and clinical challenge for medical and behavioral health providers, yet few preventive interventions have been tested for this population. This project addresses this deficit by testing the efficacy of a brief family therapy for adolescents presenting with serious risk for suicide in a primary care setting. Several innovations characterize the study. First, patients will be identified and treated directly in the primary care setting. Integrating behavioral health services into primary care may a) reduce burden on physicians by promoting parents as safety monitors, b) increase behavioral health treatment adherence, and c) address many underlying family problems associated with suicide. Second, to identify seriously at risk adolescents, we will assess for severe and persistent suicidal ideation and co-occurring depression. Patients will need to score above clinical cutoffs on both ideation (SIQ-JR \> 31) and depression (BDI-II \>20) at two consecutive appointments (generally within 3 days of each other). Third, treatment will target two of the most critical suicide risk factors: depression and family conflict. Depression is the most consistently associated risk factor for suicide and family conflict is the most common precipitant of completed suicide (20%) and non-fatal suicidal episodes (50%). Fourth, we will use Attachment Based Family Therapy (ABFT; Diamond et al., 2002) as the intervention approach, an efficacious and manualized family therapy model specifically designed for adolescent depression. ABFT has been successful in reducing suicidal ideation, hopelessness, depression, anxiety, and family conflict. Participants will be recruited from the primary care centers at The Children's Hospital of Philadelphia. Eighty-seven percent of patients are African American and 60% are girls. One hundred adolescents will be randomized to 6 to 10 weeks of either ABFT or Enhanced Usual Care (EUC). Patients will be evaluated at baseline 6, 12, 24, and 52 weeks.

Interventions

12-16 week family-based therapy

BEHAVIORALEnhanced Usual Care

Rapid referral to community outpatient care with weekly monitoring of symptoms by study team

Sponsors

Children's Hospital of Philadelphia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Suicidal ideation (SIQ-JR \> 30) * Moderate depressed mood (BDI-II \> 19) * At least one parent/caregiver willing to participate

Exclusion criteria

* Psychosis * Mental retardation or other significant cognitive impairment

Design outcomes

Primary

MeasureTime frame
Suicidal Ideation Questionnaire - JR (SIQ-JR)Baseline, 6 weeks, 12 weels, 24 weeks
Beck Depression Inventory - II (BDI-II)Baseline, 6 weeks, 12 weeks, 24 weeks
Scale for Suicidal Ideation (SSI)baseline, 6 weeks, 12 weeks, 24 weeks

Secondary

MeasureTime frameDescription
Treatment retention12 weeksNumber of treatment sessions attended.

Countries

United States

Outcome results

None listed

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