NCT03876080已完成不适用
Biomechanical Response to Dry Needling in Subjects With Delayed Onset Muscle Soreness: a Double Blind Randomized Control Trial
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 36
- 试验地点
- 2
- 主要终点
- Change in Biomechanical stiffness (N/m) using MyotonPRO
研究概览
简要总结
Investigation of the biomechanical response in delayed onset muscle soreness using dry needling vs. sham
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 35 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •The participants of the study will be any healthy male or female between
- •age of 18 to 35
- •able and willing to perform an exercise protocol using the gastrocnemius muscle
- •willing to receive either sham or dry needling intervention
排除标准
- •current muscular pain
- •prior trigger point therapy in the past 6 months
- •medications that affect muscle function
- •injury in the past 6 months
- •any health condition that prevents exercising
- •recent surgery
结局指标
主要结局
Change in Biomechanical stiffness (N/m) using MyotonPRO
时间窗: baseline, immediately after intervention, 24 hours after intervention
Measuring Biomechanical stiffness ( N/m) change at the following time frames
次要结局
- Change in Pressure pain threshold using pressure algometry(baseline, immediately after intervention, 24 hours after intervention)
研究者
Joseph Kelly
Assistant Professor
Bradley University
研究点 (2)
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