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临床试验/NCT03545880
NCT03545880已完成不适用

Effects of Kinesiotaping 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 32 人开始时间: 2018年6月6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
32
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. Different therapeutic strategies targeting to decrease post-dry needling soreness need to be investigated. Since Kinesiotaping has been advocated for decreasing tone in the muscle tissues, it would be a potential intervention for this objective.

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

  • •Generalized neck-shoulder pain with symptoms provoked by neck postures, neck movement, or palpation of the cervical musculature

排除标准

  • •any contraindication to dry needling
  • •whiplash injury;
  • •previous cervical surgery;
  • •cervical radiculopathy or myelopathy;
  • •diagnosis of fibromyalgia syndrome;
  • •having undergone any therapy intervention for the neck are in the previous 6 months;
  • •fear to needles;
  • •less than 18 or greater than 65 years of age.

研究组 & 干预措施

Kinesiotaping

Experimental

A Kinesiotaping will be provided over the upper trapezius muscle after the application of dry needling

干预措施: Kinesiotaping (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, immediately after, 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 cervical related-disability before and after the intervention(Baseline and 72 hours after treatment)
  • Changes in pressure pain sensitivity(Baseline, immediately after and 72 hours after treatment)
  • Changes in upper extremity related-disability 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

Director of Department

Universidad Rey Juan Carlos

研究点 (1)

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