Clinical Trial

Foot Intensive Rehabilitation With Perturbation Based Training in Ankle Sprain Patients

Completed
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Summary
To determine the foot-intensive rehabilitation with and without perturbation-based training on pain reduction, range of motion improvement, balance enhancement, and functional instability in patients recovering from ankle sprains NULL HYPOTHESIS There will be no significant difference in the effectiveness of foot-intensive rehabilitation with perturbation-based training compared to foot-intensive rehabilitation alone in reducing pain, improving range of motion, enhancing balance, or reducing functional instability among patients recovering from ankle sprains. ALTERNATE HYPOTHESIS There will be a significant difference in pain reduction, range of motion improvement, balance enhancement, and reduction in functional instability between patients undergoing foot- intensive rehabilitation with perturbation-based training compared to those undergoing foot-intensive rehabilitation. Study Design: It will be a Randomized Clinical Trial Study Population: Ankle Sprain Both groups will undergo the assigned interventions for the duration of 6 weeks under the supervision of trained physical therapists or healthcare professionals. The interventions will aim to address pain reduction, range of motion improvement, balance enhancement, and reduction in functional instability among participants recovering from ankle sprains.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-06-13.
Trial Details
NCT Number NCT07655973
Lead Sponsor University of Lahore
Conditions Ankle Sprain
Enrollment 36 participants
Start Date 2025-12-27
Primary Completion 2026-03-12 (estimated)
Study Completion 2026-04-27 (estimated)
Updated on ClinicalTrials.gov 2026-06-30