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临床试验/NCT00045903
NCT00045903已完成不适用

CBT Augmentation for SRI Pharmacotherapy in OCD

New York State Psychiatric Institute3 个研究点 分布在 1 个国家目标入组 136 人开始时间: 2000年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
136
试验地点
3
主要终点
Obsessive-compulsive symptoms measured at Month 2

研究概览

简要总结

This study will evaluate the effectiveness of two cognitive behavioral therapies (CBTs) in treating obsessive compulsive disorder (OCD) in patients who are taking medication but still have residual symptoms.

详细描述

Participants remain on their current OCD medication and are randomly assigned to receive one of two CBTs: exposure and ritual prevention or stress management therapy. Exposure and ritual prevention involves imaginal and in-vivo exposure and requires that participants refrain from ritualizing. Stress management involves relaxation, assertiveness training, and structured problem-solving. Therapy occurs twice per week for 2 months. Participants are assessed verbally by an independent evaluator and are asked to complete self-rating forms. Patients who respond are followed for up to 1 additional year. Participants continue to take the same medication and the same monthly therapy for the first 6 months of follow-up. During the second 6 months of follow-up, participants discontinue therapy but continue taking the same medication.

For information on a related study, please follow this link:

http://clinicaltrials.gov/show/NCT00389493

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 (Participant)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Obsessive-Compulsive Disorder (OCD) diagnosis
  • Currently taking a serotonin reuptake inhibitor (SRI, i.e. clomipramine, fluoxetine, fluvoxamine, paroxetine, sertraline, or citalopram) for OCD

排除标准

  • Medical or psychiatric conditions that would make participation in the study hazardous
  • Intensive cognitive-behavioral therapy while on an adequate dose and duration of an SRI for OCD

结局指标

主要结局

Obsessive-compulsive symptoms measured at Month 2

时间窗: 2 months

次要结局

  • General functioning measured at Month 2(2 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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