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Clinical Trials/NCT06648070
NCT06648070RecruitingNot Applicable

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

Foundation University Islamabad2 sites in 1 country44 target enrollmentStarted: July 15, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
44
Locations
2
Primary Endpoint
Neck Disability

Study Overview

Brief Summary

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 .

Detailed Description

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • IT profressionals
  • 20 - 40 years
  • Both genders
  • Diagnosed UCS
  • Pain from 2 months
  • Minimum 4 - 6 hiurs working
  • Exclusion criteria:
  • History of cervical spine
  • Trauma to neck

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Neck Disability

Time Frame: 2 weeks

It will be measured using Neck disability index

Change in ROM

Time Frame: 2 weeks

ROM will be measured with goniometer

Pain intensity

Time Frame: 2 weeks

It will be measured using Numeric pain rating scale

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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