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Completed
NCT07655973
Foot Intensive Rehabilitation With Perturbation Based Training in Ankle Sprain Patients
Conditions: Ankle Sprain
Sex: All
Ages: 18 Years – 35 Years
Healthy volunteers: No
Phase: NA
Enrollment: 36
Sponsor: University of Lahore
Location: Pakistan Sports Board Lahore Punjab Province
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.
Eligibility Criteria
Inclusion Criteria:
* • Gender: male /female
* Participants aged 18 to 35 years old.
* Diagnosis of an ankle sprain (within 4 weeks of injury).
* No prior history of severe ankle fractures or surgeries(Hoch et al., 2023)
Exclusion Criteria:
* Presence of severe or complex ankle fractures requiring surgical intervention.
* Conditions other than ankle sprain like neuropathy that affect balance or cutaneous sensation.
* Neurological disorders impacting balance or proprioception.
* Pregnancy or planning to become pregnant during the study period(Hoch et al., 2023)
Source: ClinicalTrials.gov (NCT07655973). StuddyBuddy aggregates publicly available trial information.