About this trial
The randomized controlled trail aims is to evaluate the outcome of Gongs mobilization and PNF in patients with adhesive capsulitis. The significance of this study is to compare Gong's mobilization technique with proprioceptive neuromuscular facilitation (PNF) compare their effects on pain, range of motion, and functional disability. The sample size was calculated with G-power. This study would include total 44 female participants aged 40-60 years will be recruited and randomly assigned to two groups. Group A(Gongs mobilization+ conventional therapy)and Group B(PNF+ Conventional therapy). Intervention will be provided for 4 weeks 3 session per week. Primary outcome measures are pain, ROM and functional disability via NPRS, Goniometer and U-SPADI. Outcomes will be reassessed at baseline, after 2nd week, and after 4th week.
Eligibility criteria
Qualifiers
Females in the age group between 40-60 years.
Diagnosed with Unilateral frozen shoulder.
Patients in frozen stage (progressive loss of ROM, marked stiffness with gradual pain reduction).
More than 25% painful limitation of GH ROM in two planes, more than 50% in external rotation(arm at 0 degree of abduction).
Disqualifiers
History of surgery on the affected shoulder.
Patients having any cervical or thoracic problem.
Painful, stiff shoulder after severe trauma, inflammatory diseases such as rheumatoid arthritis and malignancies.
Recent fractures in and around the shoulder.
Trial design
Treatments tested in this trial
- Gongs Mobilization
- Proprioceptive Neuromuscular Facilitation
Treatment groups
Locations
1Sponsors and collaborators
Riphah International University
Lead sponsor