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临床试验/NCT01137149
NCT01137149Unknown1 期

Behavioral Activation Therapy With Adolescents

Seattle Children's Hospital2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2006年10月最近更新:
适应症

试验速览

阶段
1 期
入组人数
60
试验地点
2
主要终点
Children's Depression Rating Scale-Revised (CDRS-R)

研究概览

简要总结

Twenty percent of adolescents will have at least one episode of clinical depression by age 18, and 65% will experience transient or less severe depressive symptoms. Depression compromises the process of adolescent development by interfering with academic, occupational, and social functioning, and increasing risk for substance use and suicide. Although initial research provides some support for both pharmacological and psychosocial interventions, many depressed teens do not respond to these interventions, and others experience a relapse of symptoms within one year. Furthermore, concerns about antidepressant medications increasing suicide risk have raised additional caution about use of pharmacotherapy with adolescents. As such, the importance of developing innovative treatment options for depressed adolescents is critical. Cognitive Behavioral Therapy (CBT) has been demonstrated to be effective in the treatment of depressed adults, with more modest efficacy data when used with children and adolescents. Interestingly, recent data from the adult literature suggests the positive outcomes of CBT can be achieved and surpassed by interventions that are purely behavioral in nature. Behavioral interventions may be easier to implement with many adolescents and may provide a better developmental fit for depressed adolescents. The present project proposes to develop a manualized Behavioral Activation (BA) Therapy for depressed adolescents, test its adaptability, acceptability, and feasibility in an open clinical trial with 12 adolescents (aged 12-17), and following further treatment refinement, test its efficacy in a randomized controlled trial of 50 adolescents (aged 12-17), in which 25 will be randomized to BA Therapy and 25 will receive "Treatment as Usual (TAU)." In this randomized controlled trial, depressed adolescents will receive 12-weeks of BA Therapy or TAU. Psychiatric and psychosocial functioning will be assessed at the beginning, middle, and end of treatment. A naturalistic follow-up will be conducted 4 and 9 months post-treatment. Assuming that BA will outperform "usual" approaches to therapy with depressed youth, the data will provide the basis for the development of a larger randomized controlled trial comparing the efficacy of BA against other widely studied approaches to the treatment of depression in youth, namely pharmacotherapy in the form of Selective Serotonin Reuptake Inhibitors (SSRIs), and CBT.

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
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

  • Age between 11 and 18;
  • one parent/legal guardian willing to participate in the study;
  • primary diagnosis of a depressive disorder (Major Depressive Disorder, Dysthymia, Depression NOS);
  • Short Mood and Feelings Questionnaire >11;
  • Children's Depression Rating Scale score > 45;
  • willingness to be randomized into either treatment group.

排除标准

  • Adolescents will be excluded if they meet any of the following criteria:
  • primary diagnosis other than a depressive disorder;
  • presence of psychotic and/or manic symptoms;
  • presence of chronic medical condition;
  • presence of active substance abuse/dependence;
  • presence of chronic self-mutilation or cutting (e.g., persistent, severe, and/or requiring medical treatment);
  • presence acute or chronic suicidality (e.g., > 3 suicidal gestures in the past year),
  • previous unfavorable response to an adequate regimen of either CBT or antidepressant treatment in the prior year, and/or (8)developmental delay.

结局指标

主要结局

Children's Depression Rating Scale-Revised (CDRS-R)

时间窗: At 9 months Follow-up Evaluaton

The CDRS-R, an interview-based measure, will be administered by the blind independent evaluator with both the parent and adolescent. The CDRS-R has been found to be a sensitive and reliable severity measure of depression in children and adolescents. Ratings are made across 17 symptoms, including depressed feelings, sleep disturbance, and suicidal ideation, on a scale of 1 (no difficulties) to 7 (severe clinically significant difficulties). A raw score at or above 45 or a T-score at or above 65 is reported to be increasingly indicative of a likely depressive disorder.

次要结局

  • Clinical Global Impressions Scale(At the 9 month follow-up evaluation)

研究者

申办方类型
Other

研究点 (2)

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