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Study identifier: NCT07576127 Synced from ClinicalTrials.gov · July 29, 2026
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Effects of Gongs Mobilization and Proprioceptive Neuromuscular Facilitation in Patients With Adhesive Capsulitis

Condition: Adhesive Capsulitis  ·  Sponsor: Riphah International University

PhaseNA
Planned participants44
Who can joinFemale, 40 Years to 60 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Fatima Miraj, DPT  ·  +923045938254  ·  fatimamiraj921@gmail.com

Attiq ur Rehman, MS  ·  +92-336-1055533  ·  attiq.rehman@riphah.edu.pk

Always discuss trial participation with your own doctor first.

Locations (1)

Pakistan Railway General HospitalRawalpindi, Punjab Province, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT07576127