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Reducing Health Risk Behavior and Improving Health in Adolescents With Depression

Reducing Health Risk Behavior and Improving Health in Adolescent Depression

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00461539
Enrollment
217
Registered
2007-04-18
Start date
2007-10-31
Completion date
2012-01-31
Last updated
2022-11-03

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

Conditions

Adolescent Health, Depression

Keywords

Tobacco Use, Alcohol and Drug Use, Obesity, Risky Sexual Behavior

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.

Interventions

OTHERTreatment as usual

Those participants receiving standard care will be referred to special programs as needed to reduce their involvement in risky health behaviors.

BEHAVIORALBehavioral health intervention

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.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Kaiser Permanente Research Foundation
CollaboratorUNKNOWN
University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to 18 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Composite health risk behavior scoreMeasured at Months 6 and 12

Secondary

MeasureTime frame
Composite International Diagnostic Interview (CIDI) depression diagnosisMeasured at Months 6 and 12
Satisfaction with care, as measured by the SF-12 health surveyMeasured at Months 6 and 12

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026