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临床试验/NCT06648070
NCT06648070招募中不适用

"Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年7月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
44
试验地点
1
主要终点
Neck Disability

研究概览

简要总结

This study is a randomised control trial and the purpose of this study is to determine the "Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome among IT professionals .

详细描述

The purpose of this study is to determine the "Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome among IT professionals

we make 2 groups control and treatment group . we give NMR technique to treatment group and PFS technique to control group in patients with upper cross syndrome.

first we take base line readings of cervical ROM , NPRS AND neck diasbilty index.

after 2 weeks of treatment again we take same readings and compare both readings.

with techniques we also perform strengthning excercise of weal muscles for both groups

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
Single (Participant)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •IT profressionals
  • •20 - 40 years
  • •Both genders
  • •Diagnosed UCS
  • •Pain from 2 months
  • •Minimum 4 - 6 hiurs working

排除标准

  • •History of cervical spine
  • •Trauma to neck

研究组 & 干预措施

NMR Group

Experimental

On group A we will perform NEUROMUSCULAR REEDUCATION TECHNIQUE:

we perform this technique on tight muscles which are:

  1. levator scapulae
  2. upper trapezius
  3. pectoralis major

干预措施: Neuromuscular reeducation technique (Procedure)

PFS Group

Experimental

On group B we perform POST FACILITATION STRETCH TECHNIQUE on tight muscles same as group A

  1. levator scapulae
  2. upper trapezius
  3. pectoralis major

干预措施: Post Facilitation Stretch (Procedure)

结局指标

主要结局

Neck Disability

时间窗: 2 weeks

It will be measured using Neck disability index

Pain intensity

时间窗: 2 weeks

It will be measured using Numeric pain rating scale

Change in ROM

时间窗: 2 weeks

ROM will be measured with goniometer

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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