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临床试验/NCT03719352
NCT03719352已完成不适用

Analysis, Comparison and Evaluation of Cervical Range of Motion and Neck Pain After Deep Dry Needling and Superficial Dry Needling in the Upper Trapezius: A Randomised Controlled Trial

Cardenal Herrera University2 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2018年10月24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
发起方
入组人数
180
试验地点
2
主要终点
Pain pressure threshold

研究概览

简要总结

This study investigates the effect of two different techniques (deep dry needling and superficial dry needling) on the latent myofascial trigger point in the upper trapezius. Subjects with latent Myofascial trigger point in this location of the muscle will be identified and will be randomly assigned to one out of the three groups: deep dry needling, superficial dry needling or sham dry needling in gastrocnemius muscle. cervical range of motion and pain pressure threshold in the upper trapezius will be registered before, immediately after the intervention, at 24 hours after the intervention, at 72 hours after the intervention and a week after the intervention

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)

盲法说明

Double (participant, outcomes Assessor

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Present the latent Myofascial trigger Point (MTP) 1 in upper trapezius.
  • Accept participation in the study (signature of informed consent).
  • Be in an age range between 18 and 55 years.
  • Do not present any

排除标准

  • Exclusion Criteria:
  • Do not present MTP 1 latent in the upper trapezius.
  • Suffering and / or having suffered from upper limb pathologies, deformities or orthopedic injuries that could alter the static and biomechanics of the shoulder and neck.
  • Not clearly identify the MTP 1 in the upper trapezius.
  • Have been diagnosed with fibromyalgia, myelopathy or radiculopathy.
  • Having contraindicated the technique of dry needling for suffering, for example, coagulation problems.
  • Having suffered a whiplash.
  • Be pregnant.
  • Have used analgesics 24 hours before participating in the study.
  • Having belonephobia.
  • Know the study techniques.
  • Be in physiotherapy treatment and / or have been treated with needle techniques at some time.
  • Having had cervical surgery.

研究组 & 干预措施

Deep dry needling

Experimental

Deep dry needling will be applied in the upper trapezius myofascial trigger point

干预措施: Experimental: Deep dry needling (Procedure)

Superficial dry needling

Experimental

Superficial dry needling will be applied in the upper trapezius myofascial trigger point

干预措施: Experimental: Superficial dry needling (Procedure)

Placebo Gastrocnemius dry needling

Placebo Comparator

A technique simulating dry needling will be applied in the gastrocnemius myofascial trigger point with a needle guard guide tube, without any therapeutic manoeuvre will be applied.

干预措施: Placebo Comparator: Placebo Gastrocnemius dry needling (Procedure)

结局指标

主要结局

Pain pressure threshold

时间窗: a week

Amount of pressure (Kg/cm2) applied at the upper trapezius myofascial trigger point site that elicit pain for the patient will be reported

次要结局

  • Cervical range of motion(a week)

研究者

发起方
Cardenal Herrera University
申办方类型
Other
责任方
Principal Investigator
主要研究者

SERGIO MONTERO NAVARRO

Principal Investigator

Cardenal Herrera University

研究点 (2)

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