Clinical Trials Directory

Trials / Completed

CompletedNCT00604097

Preventing Youth Suicide in Primary Care: A Family Model

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
66 (actual)
Sponsor
Children's Hospital of Philadelphia · Academic / Other
Sex
All
Age
12 Years – 17 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALAttachment-Based Family Therapy12-16 week family-based therapy
BEHAVIORALEnhanced Usual CareRapid referral to community outpatient care with weekly monitoring of symptoms by study team

Timeline

Start date
2004-09-01
Primary completion
2007-05-01
Completion
2008-08-01
First posted
2008-01-29
Last updated
2012-12-17

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00604097. Inclusion in this directory is not an endorsement.