跳至主要内容
临床试验/NCT04645095
NCT04645095已完成不适用

Which Type of Transcutaneous Electrical Nerve Stimulation is More Effective in Myofascial Pain Syndrome? A Randomized Controlled Trial

Ankara University2 个研究点 分布在 1 个国家目标入组 101 人开始时间: 2017年5月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
101
试验地点
2
主要终点
Pain intensity

研究概览

简要总结

The aim of this project is to compare the effects of conventional, burst and modulated TENS primarily on pain level, number of trigger points, pressure pain threshold, neck joint range of motion and disability in MAS treatment.

详细描述

Myofascial pain syndrome (MAS) is a regional pain syndrome characterized by trigger points detected by one or several muscle groups and reflected pain manifestation caused by palpation of these points. Transcutaneous electrical nerve stimulation (TENS) is a physical therapy modality that provides an analgesic effect by delivering a controlled low voltage electrical current to the nervous system through electrodes placed on the skin. Knowledge on how modulation parameters such as frequency, wave width and form alter TENS activity are limited.

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)

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

入选标准

  • Having a diagnosis of myofascial pain syndrome according to the criteria defined by Travell and Simons

排除标准

  • The onset of symptoms is less than 3 months
  • Severe cervical disc hernia, radiculopathy or myelopathy
  • Stage 3-4 cervical degeneration
  • Tumoral, infectious, psychiatric, neurological, uncontrolled systemic disease
  • Cardiac pacemaker
  • Diagnosed with fibromyalgia syndrome
  • Kyphoscoliosis
  • Acute trauma history
  • Having had previous brain or shoulder surgery
  • Injections for MAS and / or physiotherapy programs in the last 3 months
  • Pregnancy

结局指标

主要结局

Pain intensity

时间窗: Measurements will be made before treatment, at the 1st week after treatment and at the 1st month after treatment.

using Visual Analog Scale score; (0-10); 0 indicates no pain and 10 indicates worst imaginable pain

Pressure pain

时间窗: Measurements will be made before treatment, at the 1st week after treatment and at the 1st month after treatment.

using algometer (kg/cm2)

Neck joint range of motion

时间窗: Measurements will be made before treatment, at the 1st week after treatment and at the 1st month after treatment.

using double inclinometer

Number of trigger points in the upper back region

时间窗: Measurements will be made before treatment, at the 1st week after treatment and at the 1st month after treatment.

using number

Disability

时间窗: Measurements will be made before treatment, at the 1st week after treatment and at the 1st month after treatment.

using Modified Neck Disability Index

次要结局

未报告次要终点

研究者

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

Birkan Sonel Tur

Professor; MD

Ankara University

研究点 (2)

Loading locations...

相似试验