NCT00971490已完成不适用
Effects of a 4-week Acu-Transcutaneous Electrical Nerve Stimulation (Acu-TENS) Program on Subjects With Stable Chronic Obstructive Pulmonary Disease (COPD)
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
- 30
- 试验地点
- 1
- 主要终点
- Forced expiratory volume in one second (FEV1), forced vital capacity (FVC)
研究概览
简要总结
The objectives of this study are to investigate the effectiveness of Acu-TENS (transcutaneous electrical nerve stimulation applied on acupoints) on lung functions and quality of life and to explore the associated underlying mechanisms in subjects with COPD.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 50 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •clinical diagnosis with COPD
排除标准
- •allergic to gel
- •unable to perform spirometry
- •unable to communicate
- •no history of infection or exacerbation of respiratory symptoms
研究组 & 干预措施
Group 2
Placebo Comparator
干预措施: Acu-TENS (Transcutaneous electrical nerve stimulation) (Device)
Group 3
Sham Comparator
干预措施: Acu-TENS (Transcutaneous electrical nerve stimulation) (Device)
Group 1
Experimental
干预措施: Acu-TENS (Transcutaneous electrical nerve stimulation) (Device)
结局指标
主要结局
Forced expiratory volume in one second (FEV1), forced vital capacity (FVC)
时间窗: measured before and after the 4-week program
次要结局
- beta endorphin, St George Respiratory Questionnaire (SGRQ)(measured before and after the 4-week program)
研究者
研究点 (1)
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