跳至主要内容
临床试验/NCT00374439
NCT00374439已完成不适用

Promoting Well-being in Teens

Vanderbilt University1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2004年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
400
试验地点
1
主要终点
Center for Epidemiological Studies - Depression scale

研究概览

简要总结

The purpose of this study is to evaluate the efficacy of a cognitive-behavioral vs. an interpersonal therapy program for preventing depressive symptoms in adolescents.

详细描述

Hypothesis -- The cognitive-behavioral and interpersonal therapy prevention programs will be significantly better than the no-intervention control group in preventing depressive symptoms measured at post-intervention and at the 6-month follow-up. Gender differences also will be explored.

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
12 Years 至 17 Years(Child)
性别
All
接受健康志愿者
是

入选标准

  • •All students in 9th grade Wellness classes who have parental consent

排除标准

  • •Students without parental consent

研究组 & 干预措施

Cognitive-behavioral

Experimental

Participants in this arm received a cognitive-behavioral program

干预措施: Cognitive-behavioral (Behavioral)

Interpersonal Therapy

Experimental

Participants in this arm received a prevention program based on interpersonal therapy for depression

干预措施: Interpersonal Therapy (Behavioral)

No intervention

No Intervention

Participants in this arm did not receive an intervention, but complete assessments only

结局指标

主要结局

Center for Epidemiological Studies - Depression scale

时间窗: 9 weeks

Change in depressive symptoms from baseline to post-intervention at 9 weeks

Children's Depression Inventory

时间窗: 9 weeks

Change in depressive symptoms from baseline to post-intervention at 9 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Judith Garber

Professor

Vanderbilt University Medical Center

研究点 (1)

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