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
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
- 否
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
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