|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| Sponsor: | National Institute of Mental Health (NIMH) |
|---|---|
| Information provided by: | National Institute of Mental Health (NIMH) |
| ClinicalTrials.gov Identifier: | NCT00061698 |
Purpose
This study will compare the effectiveness of three therapies for the treatment of depression in preadolescent girls.
| Condition | Intervention | Phase |
|---|---|---|
|
Depression |
Behavioral: Cognitive Behavioral Therapy Behavioral: Parent Training |
Phase I |
| 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 |
| Estimated Enrollment: | 150 |
| Study Start Date: | April 2002 |
| Estimated Study Completion Date: | 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 to 13 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | R01 MH63998, DSIR 84-CTS |
| Study First Received: | June 3, 2003 |
| Last Updated: | February 5, 2007 |
| ClinicalTrials.gov Identifier: | NCT00061698 History of Changes |
| Health Authority: | United States: Federal Government |
|
Depression Mental Disorders Mood Disorders Depressive Disorder Behavioral Symptoms |