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临床试验/NCT05458206
NCT05458206已完成不适用

Effect of Mulligan Snag and Diaphragmatic Release on Thoracic Kyphosis

Cairo University4 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年10月20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
60
试验地点
4
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 mulligan snag mobilisation and diaphragmatic release on upper crossed syndrome

详细描述

Acquired postural disorders can be a consequence, to a large extent, of contemporary living and working conditions. Some of the most typical factors include continuous use of mobile phones and computers, working in sedentary jobs. Prolonged incorrect posture and reduced physical activity present a dis-balance in the musculature . It can also lead to vision issues, as well as headaches, musculoskeletal issues, and pain, as well as a multitude of other symptoms.

Upon the available research studies, there is not study conducted to investigate the effect of mulligan SNAG mobilization and diaphragmatic release in upper crossed syndrome patients this trial has four groups; one will receive diaphragmatic release + conventional, the second will receive mulligan SNAG mobilization, and conventional, the third will receive mulligan SNAG mobilization+diaphragmatic release+conventional, the fourth subjects will receive conventional

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
17 Years 至 22 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Age ranged from 17 to 22 years .
  • Body Mass Index from 20 to 25 kg/m² .
  • All participants have an intensity of neck pain on VAS (4-8) (moderate cases) .
  • The subjects were chosen from both sexes.
  • All participants have kyphosis angle ≥42°
  • All participants have mechanical neck pain and FHP (craniovertebral angle CVA < 49) CVA of < 49) .

排除标准

  • Malignancy
  • Fractures of the cervical spine
  • Cervical radiculopathy or myelopathy
  • Vascular syndromes such as vertebrobasilar insufficiency
  • Rheumatoid arthritis
  • Neck or upper back surgery
  • Taking anticoagulants
  • Local infection
  • Whiplash injury

结局指标

主要结局

pain intensity

时间窗: up to four weeks

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

次要结局

  • cervical range of motion(up to four weeks)

研究者

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

Mariam omran Grase

lecturer at basic science department, faculty of physical therapy cairo university

Cairo University

研究点 (4)

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