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临床试验/NCT02735967
NCT02735967已完成不适用

The Use of Diadynamic in Association With a Manual Therapy Program for Patients With Impingement Syndrome: a Randomized Blind Clinical Trial

University of Nove de Julho1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年3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
60
试验地点
1
主要终点
shoulder disability

研究概览

简要总结

The aim of this study will be to evaluate the effects of the use of manual therapy and diadynamic in muscle trigger points in the upper trapezius muscle in individuals diagnosed with shoulder impingement syndrome, unilateral shoulder as functional capacity, pain intensity and pain threshold the pressure.

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 (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 59 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •history of anterior lateral and unilateral shoulder pain
  • •with more than 3 months duration
  • •intensity of at least 4 points on the Numerical Rating Pain Scale
  • •positivity in at least 2 of 3 orthopedic tests for impingement syndrome: Neer, Hawkins or Jobe
  • •Associated with these characteristics volunteers should submit myofascial trigger points unilateral and active, centrally located in the trapezius muscle descending fibers associated with painful shoulder

排除标准

  • •diagnosis of bilateral impingement syndrome shoulder
  • •fibromyalgia
  • •muscle injury
  • •history of trauma on the shoulder
  • •ruptured tendons
  • •ligamentous laxity
  • •symptoms of numbness and / or tingling in the upper limbs
  • •corticosteroid injection use shoulder
  • •making use of anti-inflammatory
  • •they performed surgery or physical therapy treatment in the last 6 months in the affected shoulder.

研究组 & 干预措施

Group manual therapy + diadynamic

Experimental

Initially, the positional release techniques will be performed while maintaining this position for 90 seconds procedure is repeated 3 times. Then, the therapist performs the ischemic compression technique on the myofascial trigger point, the compression is maintained for 90 seconds by 3 replications.

Through an electrotherapy device were applied diadynamic in that myofascial trigger point previously marked. 4 minutes from the fixed two-phase mode will be applied (DF), 4 minutes long periods (LP) and 4 minutes short periods (CP), the first and second intensely in the sensitive line and the third motor threshold, both supportable according to each patient.

干预措施: manual therapy (Other)

Group manual therapy + diadynamic

Experimental

Initially, the positional release techniques will be performed while maintaining this position for 90 seconds procedure is repeated 3 times. Then, the therapist performs the ischemic compression technique on the myofascial trigger point, the compression is maintained for 90 seconds by 3 replications.

Through an electrotherapy device were applied diadynamic in that myofascial trigger point previously marked. 4 minutes from the fixed two-phase mode will be applied (DF), 4 minutes long periods (LP) and 4 minutes short periods (CP), the first and second intensely in the sensitive line and the third motor threshold, both supportable according to each patient.

干预措施: diadynamic current (Device)

Group manual therapy

Active Comparator

Initially, the positional release techniques will be performed while maintaining this position for 90 seconds procedure is repeated 3 times. Then, the therapist performs the ischemic compression technique on the myofascial trigger point, the compression is maintained for 90 seconds by 3 replications.

干预措施: manual therapy (Other)

Group diadynamic

Active Comparator

An electrotherapy device were applied diadynamic in that myofascial trigger point previously marked. 4 minutes from the fixed two-phase mode will be applied (DF),4 minutes long periods (LP) and 4 minutes short periods (CP), the first and second intensely in the sensitive line and the third motor threshold, both supportable according to each patient.

干预措施: diadynamic current (Device)

结局指标

主要结局

shoulder disability

时间窗: Change from Baseline in the Shoulder Pain and Disability Index at 4 weeks

questionnaire of quality of life developed to assess pain and associated with specific inability to shoulder disorders.

次要结局

  • intensity of pain(Change from Baseline in The Numerical rating pain scale at 4 weeks)
  • level of pressure pain(change from Baseline in ThePressure Pain Threshold at 4 weeks)

研究者

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

Cid André Fidelis de Paula Gomes

Phd

University of Nove de Julho

研究点 (1)

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