NCT01710735已完成不适用
Skeletal Muscle Contractility, Self-reported Pain and Tissue Sensitivity in Females With Neck/Shoulder Pain and Upper Trapezius Myofascial Trigger Points- a Randomized Intervention Study
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
- 80
- 试验地点
- 1
- 主要终点
- muscle contractility
研究概览
简要总结
In relation to Myofascial Triggerpoints (MFTrPs) of the upper Trapezius, this study will explore muscle contractility characteristics, the occurrence of post-intervention muscle soreness and the effect of dry needling on muscle contractile characteristics and clinical outcomes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 46 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •A clinically relevant MFTrP of the upper Trapezius musculature
- •Self-reported pain of ≥3 on an eleven-point numerical pain rating scale (NRS-101).
- •BMI less than 31
排除标准
- •a history of chronic, systemic pathology (e.g. hemophilia)
- •pre-existing neck/shoulder pathology/surgical procedures,
- •clinical depression
- •health-related legal action
- •anti-inflammatory and/or chronic pain medication
- •had received dry needling for a shoulder/neck disorder within 6 months prior to the study (to raise the level of patient naiveté) suffered from needle phobia
研究组 & 干预措施
Dry needling (deep)
Experimental
Subjects receive dry needle insertion deeper than 1,5cm below the skin of the Trapezius.
干预措施: Dry needling (Procedure)
Dry needling (superficial)
Active Comparator
Insertion of dry needle less than 1cm.
干预措施: Dry needling (Procedure)
结局指标
主要结局
muscle contractility
时间窗: 30 minutes
Measurements of maximal isometric muscle force (Fmax), and rate of force development (RDF)
次要结局
- pressure-pain threshold(60 seconds)
- NRS-101(60 seconds)
研究者
Corrie Myburgh
Dr
University of Southern Denmark
研究点 (1)
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