Comparing two techniques for treating Upper Cross Syndrome in IT professionals

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

NA · Foundation University Islamabad · NCT06648070

This study is testing whether two different treatment methods can help IT professionals with Upper Cross Syndrome feel better and move their necks more easily.

Quick facts

PhaseNA
Study typeInterventional
Enrollment44 (estimated)
Ages20 Years to 40 Years
SexAll
SponsorFoundation University Islamabad (other)
Locations1 site (Rawalpindi, Punjab Province)
Trial IDNCT06648070 on ClinicalTrials.gov

What this trial studies

This clinical trial aims to compare the effectiveness of Neuromuscular Reeducation (NMR) and Post Facilitation Stretch (PFS) techniques in treating Upper Cross Syndrome among IT professionals. Participants will be randomly assigned to either the treatment group receiving NMR or the control group receiving PFS. Baseline measurements of cervical range of motion, neck pain rating scale, and neck disability index will be taken before treatment and reassessed after two weeks. Both groups will also engage in strengthening exercises for weak muscles to enhance overall treatment outcomes.

Who should consider this trial

Good fit: Ideal candidates for this study are IT professionals aged 20 to 40 years who have been diagnosed with Upper Cross Syndrome and have experienced pain for at least two months.

Not a fit: Patients with a history of cervical spine issues, fractures, or neck trauma may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could provide effective treatment options for IT professionals suffering from Upper Cross Syndrome, potentially improving their quality of life.

How similar studies have performed: While this specific comparison may be novel, similar studies have shown positive outcomes with neuromuscular reeducation and stretching techniques in treating musculoskeletal conditions.

Eligibility criteria

Show full inclusion / exclusion 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

Where this trial is running

Rawalpindi, Punjab Province

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.

View on ClinicalTrials.gov →

Conditions: Upper Cross Syndrome

Last reviewed 2026-05-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.