Skip to main content
Clinical Trials/NCT06648070
NCT06648070
Recruiting
N/A

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

Foundation University Islamabad1 site in 1 country44 target enrollmentJuly 15, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Upper Cross Syndrome
Sponsor
Foundation University Islamabad
Enrollment
44
Locations
1
Primary Endpoint
Neck Disability
Status
Recruiting
Last Updated
last year

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

Registry
clinicaltrials.gov
Start Date
July 15, 2024
End Date
July 15, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Study Sites (1)

Loading locations...

Similar Trials