跳至主要内容
临床试验/NCT00061698
NCT00061698已完成1 期

CBT vs CBT Plus Parent Training for Girls With Depression

University of Texas at Austin0 个研究点目标入组 153 人开始时间: 2002年4月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
153

研究概览

简要总结

This study will compare the effectiveness of three therapies for the treatment of depression in preadolescent girls.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
9 Years 至 13 Years(Child)
性别
Female
接受健康志愿者

入选标准

  • Depressive Disorder

排除标准

  • Learning disability or limited intellectual ability
  • Health-related illness that would prevent the patient from completing the research study

研究者

申办方类型
Other
责任方
Sponsor

相似试验