Clinical trial Recruiting at 1 site Interventional Ages 25 to 45

Egoscue vs Feldenkrais for Upper Cross Syndrome

Official title: Comparative Effects of Egoscue and Feldenkrais Exercises on Pain, Craniovertebral Angle and Functional Disability in Upper Cross Syndrome

Run by Riphah International University · NCT07628413 · Data updated 2026-11-12

This trial compares two exercise approaches, Egoscue and Feldenkrais, to see if one can reduce neck and shoulder pain and improve posture in adults with upper cross syndrome.

Quick facts

Study typeInterventional
Ages25 Years to 45 Years
SexAll
Enrollment48 (estimated)
SponsorRiphah International University
Academic / other
Locations1 site (Lahore, Punjab Province)
StatusRecruiting
StartedDecember 15, 2025
Main results expectedJune 15, 2026
Study endsJuly 15, 2026
Registry record updatedJune 5, 2026
Trial IDNCT07628413 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 25–45 with chronic neck pain (NPRS 3–7) and a craniovertebral angle under 50 degrees who have tight pectoralis and trapezius muscles with weak rhomboids and deep neck flexors.

Probably not a fit

Individuals outside the age range, without the specified postural measurements, or with recent shoulder surgery or other exclusions may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this randomized study, adults aged 25–45 with chronic neck pain and specific postural features will be assigned to either Egoscue exercises plus conventional therapy or Feldenkrais exercises plus conventional therapy, three times weekly. The trial will measure changes in pain, the craniovertebral angle, and functional disability over the treatment period. Participants will be recruited from two Lahore clinics using simple randomization and sealed envelopes. The study uses non-probability convenience sampling for enrollment and follows standard safety exclusions related to shoulder and soft tissue conditions. Outcome data will help determine if one exercise approach offers better relief and postural improvement for upper cross syndrome.

Why it matters

Potential benefit: If successful, participants may experience reduced pain and improved posture, potentially guiding non-surgical management of upper cross syndrome.

How similar studies have gone: Prior research in posture-based therapies has shown mixed results; this study explores a direct comparison between two posture-focused exercise approaches.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 25 to 45 years
* Both genders (male and female)
* Chronic neck pain for more than three months - NPRS (3 to 7)
* Craniovertebral angle less than 50 degrees
* Tight Pectoralis muscle and trapezius
* Weak rhomboids and deep neck flexors

Exclusion Criteria:

* Any malignancy related to soft tissue and shoulder joint
* Congenital joint deformity
* Recent fractures to joint
* Recent surgery of shoulder joint or associated structures
* Patients with shoulder dislocation

Where it's running

  • Rabiya Noor
    Lahore, Punjab Province, Pakistan
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 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.