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临床试验/NCT00368771
NCT00368771已完成不适用

A Six-Month Study to Compare Outcome Differences and Visceral Response in Subjects Randomized to a Psychological Intervention for Irritable Bowel Syndrome

University of California, Los Angeles0 个研究点目标入组 163 人开始时间: 2002年7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
163
主要终点
Changes in Symptoms

研究概览

简要总结

The purpose of this study is to assess the effect of participation in one of the following interventions: (1) IBS Stress Management; (2) IBS Symptom Management; or (3) IBS Educational Training on improving IBS associated symptoms. It is anticipated that this research will provide information on the usefulness of psychological approaches in treating IBS and will help scientists better understand the disorder.

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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Irritable Bowel Syndrome

排除标准

  • GI pathology (organic disease) that affects bowel transit
  • Co-morbid pain disorders
  • Current or recent history (within 24 months) of drug or alcohol abuse
  • Clinical evidence (including physical exam, laboratory tests) of significant medical disease that may interfere with the patient successfully completing the trial
  • Planned use of drugs or agents that affect GI motility and/or perception

结局指标

主要结局

Changes in Symptoms

时间窗: 14 days

次要结局

  • IBS-Specific Beliefs and Coping(14 days)
  • IBS-specific Quality of Life increase(14 days)

研究者

申办方类型
Other
责任方
Sponsor

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