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Clinical Trials/NCT00183417
NCT00183417
Completed
N/A

Depression Prevention Program for High-Risk Adolescents

University of Texas at Austin1 site in 1 country350 target enrollmentSeptember 2004
ConditionsDepression

Overview

Phase
N/A
Intervention
Not specified
Conditions
Depression
Sponsor
University of Texas at Austin
Enrollment
350
Locations
1
Primary Endpoint
Depressive symptoms
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

This study will compare the effectiveness of two programs designed to prevent depression in adolescents.

Detailed Description

Major depression is one of the most common psychiatric disorders in adolescents. In many cases, the condition is recurrent and can result in serious psychological impairment. A high number of depressed adolescents never receive treatment; therefore, it is crucial to develop prevention programs for this disorder that are effective and can be easily disseminated. This study will evaluate and compare the effectiveness of cognitive behavior therapy (CBT) and supportive/expressive (S/E) therapy in preventing depressive symptoms in adolescents. This study will last 2 years. Participants will be randomly assigned to receive six sessions of CBT, S/E therapy, or standard depression education over 2 years. The CBT intervention will focus on reducing negative thoughts and increasing engagement in pleasant activities. S/E therapy is designed to allow adolescents to express their negative emotions and talk about recent stressful events in a supportive environment of their peers. Surveys and psychiatric interviews will be completed by all participants and their parents at the beginning and the end of the study. The surveys and interviews will assess depressive symptoms.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
May 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Beck Depression Inventory score higher than 10
  • Parent or guardian willing to provide informed consent

Exclusion Criteria

  • Diagnosis of depression

Outcomes

Primary Outcomes

Depressive symptoms

Time Frame: Measured at Year 1

Study Sites (1)

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