Actively Recruiting
Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals
Led by Foundation University Islamabad · Updated on 2025-07-11
44
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of Neuromuscular Reeducation (NMR) compared to Post Facilitation Stretch (PFS) technique for treating Upper Cross Syndrome among IT professionals aged 20 to 40 years. The study aims to determine how these two physical therapy methods impact pain, posture, muscle balance, and cervical range of motion in people who have been experiencing symptoms for at least two months. This randomized control trial involves two distinct groups to compare these approaches directly. Participants are divided into two groups: Group A receives Neuromuscular Reeducation, and Group B receives Post Facilitation Stretch. Both groups undergo a treatment protocol consisting of seven sessions over two weeks on alternate days. Each session begins with a 10-minute hot pack application to the cervical area, followed by the assigned technique applied to tight muscles including the levator scapulae, upper trapezius, and pectoralis major. Both groups also perform strengthening exercises targeting rhomboids, lower and middle trapezius, and deep flexors. During the study, researchers will assess participants' cervical range of motion using a goniometer, pain levels with the Numeric Pain Rating Scale (NPRS), and neck disability using the Neck Disability Index at baseline and after two weeks of treatment. These measurements will be compared to evaluate the effectiveness of each technique. The study is conducted by Foundation University Islamabad and participation lasts for two weeks with assessments before and after the treatment period.
CONDITIONS
Brief Title
Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals
Who Can Participate
Eligibility Criteria
You may qualify if you...
- IT professionals aged 20 to 40 years
- Both genders
- Diagnosed with Upper Cross Syndrome
- Experiencing pain for at least 2 months
- Working a minimum of 4 to 6 hours daily
You will not qualify if you...
- History of cervical spine fracture
- History of trauma to the neck
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 weeks
Participants receive either neuromuscular reeducation or post facilitation stretch technique along with strengthening exercises over a period of 2 weeks.
7 sessions on alternate days
Duration - Immediately after 2 weeks of treatment
After completing treatment, participants have their pain, posture, muscle balance, and cervical range of motion assessed again.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Foundation University College of Physical Therapy
Islamabad, Pakistan, 44000
Actively Recruiting
Research Team
H
Hina Ayub, DPT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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