NCT01635634已完成不适用
Randomized Controlled Pilot Trial: The Effectiveness of Cupping in Patients With Fibromyalgia
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
- 141
- 试验地点
- 1
- 主要终点
- Pain Intensity
研究概览
简要总结
The purpose of this randomized controlled study is to determine the effectiveness of cupping in patients with fibromyalgia compared to sham cupping.
详细描述
see above
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
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •FMS diagnosis according to AWMF Guidelines,
- •necessary documents: medical records
- •Pain intensity > 45mm VAS
- •Participation in cupping twice weekly on appointment
排除标准
- •pregnancy
- •other study participation
- •pain due to other rheumatic disease
- •major psychiatric disorder
- •substance abuse
- •severe somatic disorder (cancer)
- •injections, acupuncture, neural therapy within the past 3 months
研究组 & 干预措施
Sham Cupping
Sham Comparator
Dry Cupping Therapy 5 serial treatments twice weekly 4-8 cups at the upper and lower back
干预措施: Cupping therapy (Other)
Cupping Therapy
Experimental
Dry Cupping 5 serial treatments twice weekly 4-8 cups at the upper and lower back
干预措施: Cupping therapy (Other)
Wait list
No Intervention
Wait list control no specific intervention for 3 weeks study period
结局指标
主要结局
Pain Intensity
时间窗: Day 18
Pain on a 100mm visual analog scale
次要结局
- Fatigue(Day 200)
- Sleep Quality(Day 200)
- Quality of life(Day 200)
- Medication(Day 18)
- Pain Intensity(Day 200)
- adverse events(Day 18)
- Pressure pain sensitivity(Day 18)
- Disability(Day 200)
- Fatigue(Day 18)
- Sleep Quality(Day 18)
- Quality of life(Day 18)
- Disability(Day 18)
研究者
Jost Langhorst
Prof. Dr. med.
Universität Duisburg-Essen
研究点 (1)
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