Actively Recruiting

Phase Not Applicable
Age: 20Years - 45Years
All Genders
NCT07573553

Effectiveness of Rib Mobilization Combined With Postural Correction Exercises in Individuals With Upper Crossed Syndrome

Led by Riphah International University · Updated on 2026-05-07

64

Participants Needed

1

Research Sites

36 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled trial aims to evaluate the effectiveness of rib mobilization combined with postural correction exercises in reducing pain, improving cervical posture, and enhancing rib and thoracic mobility among individuals with Upper Crossed Syndrome (UCS). A total of 64 participants aged 20-45 years will be recruited and randomly assigned to two groups: Group A (rib mobilization + postural correction) and Group B (postural correction only). Intervention will be provided for 4-6 weeks, three sessions per week. Outcomes will include pain (VAS), cervical posture (inclinometer), and rib/thoracic mobility (tape measure). Data will be analyzed using SPSS version 26.

CONDITIONS

Official Title

Effectiveness of Rib Mobilization Combined With Postural Correction Exercises in Individuals With Upper Crossed Syndrome

Who Can Participate

Age: 20Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 20 to 45 years
  • Forward head posture (craniovertebral angle less than 50 degrees)
  • Cervical pain or discomfort lasting 4 weeks or more
  • Moderate pain intensity with a visual analogue scale score between 3 and 6
  • Willingness to participate and provide informed consent
  • Clinically diagnosed Upper Crossed Syndrome (UCS)
  • Meets Asian Fitness Society diagnostic criteria for UCS
Not Eligible

You will not qualify if you...

  • History of trauma or surgery to the cervical or thoracic spine
  • Cervical disc herniation, radiculopathy, or neurological deficits
  • Structural deformities such as scoliosis or Scheuermann's disease
  • Systemic musculoskeletal disorders like rheumatoid arthritis
  • Vestibular, balance, or visual disorders
  • Received similar therapy within the last 3 months
  • Pregnancy or contraindication to manual therapy
  • Current use of pain medications or muscle relaxants

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

District Headquater Haripur

Chak Six Hundred Twenty-four, Khyber Pakhtunkhwat, Pakistan, 22620

Actively Recruiting

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Research Team

A

Altamash Hussain Khan, DPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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