Clinical Trials Directory

Trials / Completed

CompletedNCT00073671

Prevention of Depression in At-Risk Adolescents

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
316 (actual)
Sponsor
Vanderbilt University · Academic / Other
Sex
All
Age
13 Years – 17 Years
Healthy volunteers
Not accepted

Summary

This study examines the impact of a group cognitive behavioral program aimed at preventing depressive disorders and symptoms in adolescents at risk for developing depression.

Detailed description

Depression is a prevalent, chronic, and impairing condition that is often undetected and becomes more difficult to treat as chronicity increases. There is an increasing need to conduct large-scale depression prevention studies in adolescents. This study evaluates a cognitive-behavioral prevention (CBP) program to determine its effectiveness in preventing depressive disorders in at-risk adolescents. The study also will ascertain the costs this intervention to inform attempts at future dissemination of the program in "real world" settings. Participants in this study are randomly assigned to receive either CBP for eight weekly and 6 monthly continuation sessions or usual care. Depressive symptoms and disorders, levels of functioning, and medical and mental health care utilization are assessed at baseline and again at 2, 8, 20, and 32 months after intake.

Conditions

Interventions

TypeNameDescription
BEHAVIORALCognitive-behavioral prevention programCognitive-behavioral prevention program includes 8 weekly and 6 monthly group sessions.
OTHERUsual careParticipants receive usual care

Timeline

Start date
2003-03-01
Primary completion
2006-03-01
Completion
2009-01-01
First posted
2003-12-03
Last updated
2022-01-31

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00073671. Inclusion in this directory is not an endorsement.