"Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals
Recruiting
N/A
Interventional Study
Upper Cross Syndrome
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 20 – 40
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 44 (estimated)
- Sponsor
- Foundation University Islamabad · Other
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About This Trial
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 .
Trial Locations
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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
* Fracture
* Trauma to neck
Contacts