Depression |
Depression/depressive Disorders |
Clinical Trial: Treatment for Depressed Preadolescent Girls
This study is currently recruiting patients.
|
Purpose
The purpose of this study is to compare the effectiveness of three therapies for the treatment of depression in preadolescent girls.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Depression | Behavior: Cognitive Behavioral Therapy Behavior: Parent Training | Phase I |
MedlinePlus related topics: Depression
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: CBT vs CBT plus Parent Training for Girls with Depression
Expected Total Enrollment: 150
Study start: April 2002; Expected completion: April 2007
Depressive disorders during childhood are virulent, long-lasting disorders that are a risk factor for the development of future depressive episodes and other psychiatric difficulties. A dysfunctional family environment is a possible pathway to the development of depression in adolescents. The family environment is an especially salient context for the development of depression in preadolescent girls.
Depression is expressed differently between male and female adolescents; girls may not benefit as much as boys from treatments such as cognitive behavioral therapy (CBT) because the treatments may not target disturbances and skills that are specific to preadolescent girls. This study will identify effective treatments for depression in preadolescent girls.
Depressed participants are randomly assigned to receive CBT, CBT plus parent training (PT), or a minimal contact control (MCC). The CBT group receives treatment twice a week for 10 weeks. Participants in the CBT plus PT group receive therapy sessions and group treatment for 10 weeks. Participants in the MCC group meet with a research associate once a week for 10 weeks. During the control visits, the child's depressive symptoms are assessed, but no advice or treatment is given. Participants are assessed at baseline, post-treatment, and at yearly follow-up visits for up to 4 years. School performance, home environment, and the impact of the interventions on parent adjustment are evaluated.
Eligibility
Ages Eligible for Study: 9 Years - 13 Years, Genders Eligible for Study: Female
Criteria
Inclusion Criteria:
- Depressive Disorder
Exclusion Criteria:
- Learning disability or limited intellectual ability
- Health-related illness that would prevent the patient from completing the research study
Location and Contact Information
Texas
University of Texas at Austin, Austin, Texas, 78628, United States; Recruiting
More Information
Record last reviewed: January 2005
Last Updated: January 25, 2005
Record first received: June 3, 2003
ClinicalTrials.gov Identifier: NCT00061698
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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