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临床试验/NCT02558686
NCT02558686已完成不适用

Effects of Eccentric Exercise, Sham or Placebo on Post-Needling Soreness by Dry Needling on Active Trigger Points

Universidad Rey Juan Carlos1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2015年10月1日最近更新:
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
90
试验地点
1
主要终点
Changes in post-dry needling pain intensity before and after the intervention

研究概览

简要总结

Application of trigger point dry needling can induce post-dry needling soreness. This is not a negative experience, but sometimes some patients want to reduce it as much as possible. Manual therapies and exercise strategies targeting to decrease post-dry needling soreness need to be investigated.

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
Triple (Participant, Investigator, Outcomes Assessor)

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

  • •Unilateral non-traumatic shoulder pain
  • •Shoulder pain from at least 6 months
  • •Shoulder pain of more than 3 points on a NPRS
  • •Presence of active trigger point in the infraspinatus muscle

排除标准

  • •bilateral shoulder pain
  • •younger than 18 or older than 65 years
  • •shoulder injury
  • •upper extremity surgery
  • •fibromyalgia syndrome
  • •neck or shoulder surgery
  • •cervical radiculopathy
  • •any type of intervention for the neck-shoulder the previous year

研究组 & 干预措施

Eccentric Exercise

Experimental

Individuals will perform 3 sets of 10 repetitions of eccentric exercise of the infraspinatus muscle after the application of trigger point dry needling

干预措施: Eccentric Exercise (Other)

Detuned Ultrasound

Sham Comparator

Individuals will received 10 minutes of detuned ultrasound on the infraspinatus muscle after the application of trigger point dry needling

干预措施: Detuned Ultrasound (Other)

Placebo

Placebo Comparator

Individuals will not perform any action after the application of trigger point dry needling

干预措施: Placebo (Other)

结局指标

主要结局

Changes in post-dry needling pain intensity before and after the intervention

时间窗: Baseline, 24 hours after, 48 hours after and 72 hours after treatment

A Numerical Pain Rate Scale (NPRS, 0-10) will be used to record post-dry needling soreness and pain

次要结局

  • Changes in spontaneous shoulder pain before and after the intervention(Baseline and 72 hours after treatment)
  • Changes in disability before and after the intervention(Baseline and 72 hours after treatment)
  • Changes in functionality before and after the intervention(Baseline and 72 hours after treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

César Fernández-de-las-Peñas

Head Division

Universidad Rey Juan Carlos

研究点 (1)

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