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Clinical Trials/NCT06741033
NCT06741033
Active, not recruiting
Not Applicable

Comparing the Effect of Toe-in Gait Modification Along With Conventional Physiotherapy in People With Medial Knee Osteoarthritis

Superior University1 site in 1 country34 target enrollmentFebruary 28, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Superior University
Enrollment
34
Locations
1
Primary Endpoint
NUMERIC PAIN RATING SCALE (NPRS)
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

Medial knee osteoarthritis (OA) remains a prevalent and debilitating condition, despite conventional physiotherapy interventions aimed at reducing pain and improving function. This study investigates the additional benefits of toe-in gait modification when combined with conventional physiotherapy in individuals with medial knee OA. Rooted in biomechanical theories suggesting that altering gait patterns can reduce medial knee load, this research employs a randomized controlled trial methodology.

Detailed Description

Participants are divided into two groups: one receiving conventional physiotherapy alone, and the other receiving a combination of conventional physiotherapy and toe-in gait modification. Outcomes are assessed over a 8-week period, focusing on pain levels and physical function. The significance of this study lies in its potential to enhance current treatment protocols, offering a more effective, non-invasive intervention to alleviate symptoms and improve the quality of life for those suffering from medial knee OA. The findings could inform clinical practices and pave the way for personalized rehabilitation strategies that incorporate gait modifications, ultimately reducing the healthcare burden associated with knee osteoarthritis.

Registry
clinicaltrials.gov
Start Date
February 28, 2024
End Date
March 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Muhammad Naveed Babur

Principal Investigator

Superior University

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of MKOA having Grade 1-3 (radiographic evidence of MKOA)
  • Knee pain on most days of previous month. (The most symptomatic side will consider the study limb for participants with bilaterally eligible knees)
  • Age \> 45
  • Ability to walk unaided for at least 25 min
  • Gender eligibility both male and female

Exclusion Criteria

  • Severe MKOA (Grade 4)
  • Lateral OA
  • Patella femoral OA
  • Previous or planned hip or knee surgery
  • Hip or ankle arthritis
  • Rheumatoid arthritis
  • Severe valgus and varus alignment requiring the use of an assistive device and the inability to walk independently
  • Neurological dysfunction

Outcomes

Primary Outcomes

NUMERIC PAIN RATING SCALE (NPRS)

Time Frame: 12 Months

The NPRS is 11-point numeric scale ranges from '0' representing "no pain" to '10' representing "pain as bad as you can imagine

WOMAC scale

Time Frame: 12 Months

The Western Ontario and McMaster Universities Arthritis Index (WOMAC) is widely used in the evaluation Knee Osteoarthritis. It is a self-administered questionnaire consisting of 24 items divided into 3 subscales (Pain, Stiffness, and Physical Function) The scores for each subscale are summed up, with a possible score range of 0-20 for Pain, 0-8 for Stiffness, and 0-68 for Physical Function. Usually a sum of the scores for all three subscales gives a total WOMAC score.

Study Sites (1)

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