Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07025993

Effects of Muscle Energy Technique Versus Cervical and Scapulothoracic Stabilization Exercises in Upper Crossed Syndrome

Led by Riphah International University · Updated on 2025-06-18

34

Participants Needed

1

Research Sites

30 weeks

Total Duration

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AI-Summary

What this Trial Is About

This study will be a randomized clinical trial and will be conducted in Younus Hospital, Tehsil headquarters hospital Daska, and Riphah Rehabilitation Clinic Lahore. Non-probability consecutive sampling will be used to collect the data. A sample size of 40 subjects with an age group between 18-65 years will be taken. Data will be collected from the patients having present complaints of Neck pain associated with upper cross syndrome. Outcome measures will be taken using the Numeric Rating Pain Scale (NRPS) for pain and the Neck disability index (NDI) for neck functional health and craniovertebral angle for posture. An informed consent will be taken. Subjects will be selected based on inclusion and exclusion criteria and will be equally divided into two groups by a random number generator table. Both Groups will receive Moist Hot Pack, Cervical segmental mobilizations, and Free Neck Exercises (AROMs), while Group A will receive Muscle energy technique(eccentric muscle energy technique for the cervical spine with Mets for upper trapezius, Suboccipitalis and pectoralis muscle), and Group B will receive cervical and scapulothoracic stabilization exercises(axial elongation exercise, craniocervical flexion, cervical extension and Cervico-scapulothoracic stabilization exercises). Outcome measures will be measured at baseline and after 4 weeks. Data analysis will be done by SPSS version 25.

CONDITIONS

Official Title

Effects of Muscle Energy Technique Versus Cervical and Scapulothoracic Stabilization Exercises in Upper Crossed Syndrome

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female diagnosed with upper crossed syndrome
  • Neck pain lasting between 4 and 12 weeks
  • Neck pain rated 6 or higher on the Numeric Rating Pain Scale
  • Willingness to sign the written consent form
Not Eligible

You will not qualify if you...

  • Diagnosed with tuberculosis, carcinoma, heart disease, or osteoporosis within the last 6 months
  • Neural disorders from prolapsed intervertebral disc
  • History of trauma or infection in the neck area
  • Upper motor neuron disease, cervical stenosis, or metabolic bone and joint diseases
  • Hyper flexibility
  • Presence of open sores
  • Currently receiving radiotherapy, chemotherapy, steroid therapy, or anticoagulants
  • Psychiatric conditions such as phobia, obsession, or depression
  • Allergy to hot packs

AI-Screening

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Trial Site Locations

Total: 1 location

1

Riphah Rehabilitation Clinic

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

S

Syed Shakil ur Rehman, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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