Actively Recruiting
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
On this page
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
Eligibility Criteria
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
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
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Trial Site Locations
Total: 1 location
1
Riphah Rehabilitation Clinic
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
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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