Actively Recruiting
Bowen Technique Versus Dynamic Soft Tissue Mobilization on Pain, Range of Motion and Functional Disability in Patients With Adhesive Capsulitis
Led by University of Lahore · Updated on 2025-07-02
72
Participants Needed
1
Research Sites
24 weeks
Total Duration
On this page
Sponsors
U
University of Lahore
Lead Sponsor
U
University of Lahore Hospital (ULH)
Collaborating Sponsor
AI-Summary
What this Trial Is About
A randomized controlled trial included 72 patients diagnosed with adhesive capsulitis will conduct in University of Lahore Teaching Hospital. The study will complete within 9 months after the approval of synopsis. Patients who fulfilled the inclusion criteria will identified by individual physiotherapist and will enrolled for particular study. Informed written consent will be taken by the patients and will randomly allocated into two groups. The total numbers of sessions will 12 (3 sessions per week). The study will single blinded. The assessor will unaware of the treatment given to both groups. Control group received routine physical therapy with dynamic soft tissue mobilization technique. thermotherapy, trans-cutaneous electrical nerve stimulation, shoulder isometrics and stretching that includes 12 sessions and three times per week. Experimental group received routine physical therapy along with Bowen technique. This includes thermotherapy, trans-cutaneous electrical nerve stimulation, shoulder isometrics and stretching that includes 12 sessions and three times per week
CONDITIONS
Official Title
Bowen Technique Versus Dynamic Soft Tissue Mobilization on Pain, Range of Motion and Functional Disability in Patients With Adhesive Capsulitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed patients aged 50 to 80 years
- Grade 2 and 3 (frozen and thawing) adhesive capsulitis
- Patients willing to participate in the study
- Only diabetic patients
You will not qualify if you...
- Major mental health problems
- History of shoulder surgery or other shoulder diseases including rotator cuff tear, subacromial impingement syndrome, and shoulder labral tear
- Use of oral or intra-articular steroids and cortisone injections within the prior 3 months
- Rotator cuff tears or other shoulder ligament injuries, history of shoulder arthritis, malignancy
- Adhesive capsulitis secondary to fractures, dislocation, reflex sympathetic dystrophy, or neurological disorder
AI-Screening
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Trial Site Locations
Total: 1 location
1
UOL Teaching Hospital
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
D
Dr farrukh Murtaza Physical Therapist, Phd (PT)*
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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