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 2024-10-18
44
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the effects of two different physical therapy techniques, Neuromuscular Reeducation (NMR) and Post Facilitation Stretch (PFS), on Upper Cross Syndrome among IT professionals. The study involves adults aged 20 to 40 years who have been diagnosed with this condition and have experienced pain for at least two months. The goal is to compare these techniques for improving symptoms related to this syndrome. Participants are divided into two groups: one group receives the NMR technique, which involves deep pressure along the muscles from origin to insertion combined with active movement and rest periods. The other group receives the PFS technique, which consists of isometric muscle contractions followed by rapid stretching and relaxation. Both groups also perform strengthening exercises for weak muscles as part of their treatment. The treatments are applied specifically to tight muscles including the levator scapulae, upper trapezius, and pectoralis major. Before treatment, baseline measurements are taken for neck range of motion (ROM), pain intensity using the Numeric Pain Rating Scale (NPRS), and neck disability index. After two weeks of treatment, these measures are repeated to assess changes. Participants undergo assessments at the start and after two weeks to compare improvements. The study monitors neck function, pain levels, and disability related to the syndrome throughout 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 between 20 and 40 years
- Both male and female 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 problems
- Previous fractures
- 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 techniques along with strengthening exercises for weak muscles to address Upper Cross Syndrome.
Baseline visit and follow-up visit after 2 weeks
Trial Site Locations
Total: 1 location
1
Foundation University College of Physical Therapy
Rawalpindi, Punjab Province, Pakistan, 46000
Actively Recruiting
Research Team
H
Hina Ayub, MS-MSKPT
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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