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Clinical Trials/NCT00461539
NCT00461539
Completed
Phase 1

Reducing Health Risk Behavior and Improving Health in Adolescent Depression

University of California, Los Angeles2 sites in 1 country217 target enrollmentOctober 2007

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Depression
Sponsor
University of California, Los Angeles
Enrollment
217
Locations
2
Primary Endpoint
Composite health risk behavior score
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This study will determine the effectiveness of a health education intervention in reducing health risk behavior and improving health in adolescents with depression.

Detailed Description

Depression is a common disorder among adolescents. If left untreated, it can cause significant disability, illness, and even death. Teens with depression often engage in risky health behaviors, such as smoking, drug and alcohol use, unprotected sex, and unhealthy eating and exercise patterns. By reducing these health risk behaviors, depressed adolescents may be able to avoid negative health consequences and improve their physical and mental health. This study will determine the effectiveness of a health education intervention in reducing risky health behaviors in adolescents with depression. Participants in this study will be invited to enroll during a visit to a participating primary care clinic. Participants will be randomly assigned to either partake in a health education intervention or receive standard care. Both groups will continue to receive treatment through their primary care clinic. Those participants receiving standard care will be referred to special programs as needed to reduce their involvement in risky health behaviors. Participants assigned to the health education intervention will attend 10 weekly education sessions that will be led by trained health educators. Parents or guardians may be asked to attend sessions depending on their interest in the intervention and the age of the youth participant. Topics covered will include teenage smoking, alcohol and drug abuse, risky sexual behaviors, and obesity. Cognitive-behavioral strategies, role playing, and media clips will be used to stimulate discussion and involvement in the intervention. The intervention will be tailored to target the specific risky behaviors in which each participant engages. Motivational interviewing will also be used to build positive attitudes to support behavior change. All participants will attend follow-up visits to assess behavior change at Months 6 and 12 following study entry.

Registry
clinicaltrials.gov
Start Date
October 2007
End Date
January 2012
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Joan Asarnow

Professor of Psychiatry & Biobehavioral Sciences

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • CIDI diagnosis of major depression or probable depression based on youth self report
  • Availability of a family member to provide informed consent

Exclusion Criteria

  • Lacks contact information (e.g., address, telephone number)
  • Any functioning deficits or other characteristics that might interfere with study participation
  • Currently in a living situation that might interfere with study participation (e.g., lives over 1 hour away from the study site)
  • Lacks family available to participate in the intervention
  • Mental retardation
  • Does not speak English or Spanish

Outcomes

Primary Outcomes

Composite health risk behavior score

Time Frame: Measured at Months 6 and 12

Secondary Outcomes

  • Satisfaction with care, as measured by the SF-12 health survey(Measured at Months 6 and 12)
  • Composite International Diagnostic Interview (CIDI) depression diagnosis(Measured at Months 6 and 12)

Study Sites (2)

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