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Study identifier: NCT07731737 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effects of Pressure Biofeedback Training Versus Bolster Foam Roll Training for Pain, Muscles Activation, and Quality of Life Among Knee Osteoarthritis Patients

Condition: Knee Osteoarthritis (Knee OA) · Knee Arthritis, Osteoarthritis  ·  Sponsor: Lahore University of Biological and Applied Sciences

PhaseNA
Planned participants48
Who can joinAll sexes, 45 Years to 65 Years
Healthy volunteersNo

About this study

The current study will be a single-blinded, two-arm parallel group randomized clinical trial involving 48 participants. The trial will compare Pressure Biofeedback training with Bolster Foam Roll training. Interventions will be delivered three times per week for eight weeks. The primary outcomes will include pain intensity, functional status, and muscle activation. Assessments will be conducted at baseline (week 0), mid-intervention (week 4), post-intervention (week 8), and follow-up (week 12). The study will be conducted at the outpatient departments of Sir Ganga Ram Hospital (SGRH) and Mayo Hospital Lahore. The hypothesis is that there is a difference between Pressure Biofeedback Training and Bolster Foam Feedback Training regarding pain reduction, muscle activation, and patient-reported quality of life compared to Bolster Foam rolling training among knee osteoarthritis patients.

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

Talk to the study team

Sahar Fatima, Sidra Principal Investigator  ·  +923271202200  ·  sahar.fatima@ubas.edu.pk

Dr. Shoaib Waqas Waqas

Always discuss trial participation with your own doctor first.

Locations (1)

Lahore University of Biological and Applied SciencesLahore, PakistanRecruiting

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Source record: clinicaltrials.gov/study/NCT07731737