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临床试验/NCT04702100
NCT04702100已完成不适用

Instrument-assisted Soft Tissue Mobilization Versus Integrated Neuromuscular Inhibition Technique on Mechanical Non-specific Neck Pain

Cairo University2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年1月1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
90
试验地点
2
主要终点
pain intensity

研究概览

简要总结

the aim of this study is to investigate the efficacy of instrumented assisted soft tissue mobilization versus integrated neuromuscular inhibition technique on mechanical non-specific neck pain

详细描述

Mechanical neck pain is a prevalent condition in various populations. Neck pain occurrence is affected by several factors, involving environmental, psychological, and social aspects. Neck pain represents the fourth major disorder responsible for a person's year lived with disability and ranked eleventh as disability-adjusted life years of a person. The neck pain incidence ranges from 10.4 to 23.3% in 1-year time, while the range of prevalence was 0.4 to 86.8%. It has a high prevalence among computer users, office workers, and females, especially females aged 35 to 49 years old. Myofascial trigger point (MTrP) might play an important role in the formation of mechanical neck pain and is known as a hyperirritable spot in skeletal muscle that is accompanied with a hypersensitive palpable nodule in a taut band. IASTM and integrated play an important role in the treatment of mechanical neck pain.this trial has three groups; one will receive IASTM+ conventional, the second will receive integrated + conventional and the third will receive conventional treatment for four week

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

random generator

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • diagnosed as non-specific neck pain with upper trapezius active myofascial trigger points less than 3 months of duration and have these criteria: taut band on palpation, hyper sensible tender spot in the taut band, local twitch response referred pain pattern
  • body mass index from 18 to 25 kg/m2
  • their ages from 18-35

排除标准

  • if they had trigger point injections within the past 6 months
  • history of neck or upper back surgery, trauma or fracture
  • history of a whiplash injury, skin diseases and lesions, any sensory disturbances, any vascular syndromes, neck and back deformities
  • cervical radiculopathy, and diagnosis of fibromyalgia syndrome, skin diseases

结局指标

主要结局

pain intensity

时间窗: up to four weeks

The scale that will be used the VAS ;each subject will instructed to put point on line from no pain to tolerable pain

次要结局

  • neck disability(up to four weeks)
  • muscle amplitude in the form of normalized root mean square (RMS)(up to four weeks)
  • muscle fatigue in the form of median frequency(up to four weeks)

研究者

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

Al Shaymaa Shaaban Abd El Azeim

principle investigator

Cairo University

研究点 (2)

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