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临床试验/NCT00158301
NCT00158301已完成不适用

Continuation Phase CBT for Youth With MDD

University of Texas Southwestern Medical Center1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2004年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
72
试验地点
1
主要终点
Relapse of depressive symptoms

研究概览

简要总结

This study will determine the effectiveness of cognitive behavioral therapy in preventing a relapse of depressive symptoms in children.

详细描述

Depression is a chronic and episodic condition that may have devastating effects on social and emotional functioning, particularly in the pediatric population. While approximately 90% of children eventually recover from an episode of depression, up to 40% of those children relapse within 1 to 2 years. Data indicate that cognitive behavioral therapy (CBT) delivered after depressive symptoms subside can significantly reduce depression relapses in adults. However, there are no comparable studies in children or adolescents. This study will determine whether CBT is effective in reducing a relapse of depressive episodes in children and adolescents with major depression.

This study comprises two phases. In Phase 1, all participants will receive drug treatment for 12 weeks. Participants who respond to the treatment will complete the study after 12 weeks. Participants whose depression symptoms return after 12 weeks will be enrolled in Phase 2. In Phase 2, participants will be randomly assigned to either continue drug therapy alone or to receive drug therapy plus CBT for 6 months. The CBT will focus on teaching participants skills to manage depressed moods and to identify situations which might put them at risk for a relapse in depressive symptoms. Self-report scales will be used to assess the depressive symptoms of participants who complete Phases 1 and 2 at study entry and at the end of the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
11 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of nonpsychotic major depressive disorder at least 4 weeks prior to study entry
  • Clinical Global Impression severity score of 4 or greater
  • Children's Depression Rating Scale score of 40 or greater
  • Currently attending school
  • Willing and able to use acceptable methods of contraception, if applicable
  • In good general health
  • Parent or guardian willing to provide informed consent, if applicable

排除标准

  • History of psychotic disorders
  • Alcohol or substance abuse or dependence within 6 months prior to study entry
  • History of anorexia nervosa or bulimia
  • Chronic medical illness requiring regular medication
  • Current use of medication with psychotropic effects
  • First-degree relatives (e.g., mother, father, sister, brother) with bipolar I disorder
  • At risk for suicide
  • Failure of a previous adequate treatment with fluoxetine (defined as at least 40 mg/day for 4 weeks)
  • IQ less than 80
  • Pregnancy or breastfeeding

研究组 & 干预措施

1

Experimental

Continuation phase cognitive behavioral therapy and drug therapy for 6 more months following acute treatment response

干预措施: Cognitive behavioral therapy (CBT) (Behavioral)

1

Experimental

Continuation phase cognitive behavioral therapy and drug therapy for 6 more months following acute treatment response

干预措施: Drug therapy (Drug)

2

Active Comparator

Continuation phase drug therapy only for 6 more months following acute treatment response

干预措施: Drug therapy (Drug)

结局指标

主要结局

Relapse of depressive symptoms

时间窗: Measured at Months 3 and 9

次要结局

未报告次要终点

研究者

研究点 (1)

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