To check the Consistency and Accuracy of the Balance measures using Pedalo® -Sensamove-Balance device in population with Knee osteoarthritis

Not Applicable

• Conditions: Health Condition 1: M171- Unilateral primary osteoarthritisof knee

• Registration Number: CTRI/2023/03/050709
• Lead Sponsor: Jamia Millia Islamia

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 3 April 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Diagnosis of unilateral knee osteoarthritis based on radiographic findings using Kellgren and Lawrence classification

Knee pain of more than 4 months duration

Scores from 3-6 on NPRS

Ability to walk independently

Normal or corrected to normal hearing

Normal or corrected to normal vision

Exclusion Criteria

History of lower extremity joint replacement surgery

Patients who had any other surgeries or suffered from injuries to lower extremities in the 12 months prior to the study

BMI >= 40 kg/m² (Obese class III)

Any other cardiovascular or neurological disorders which could affect balance

Vestibular or neuromuscular system impairment

Patients who had received any intra-articular injections in the last 90 days

Any medical treatment that might impair balance

Any systemic arthritic condition

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Centre of pressure (COP) range <br/ ><br>2.Centre of pressure (COP) sway <br/ ><br>3.Proprioception <br/ ><br>4.Reaction time <br/ ><br>5.Multidirectional stabilityTimepoint: For test-retest reliability, at Day 1 and after 1 week

Secondary Outcome Measures

Name	Time	Method
1. Functional Reach Test (FRT) <br/ ><br>2. One Leg Standing (OLS) <br/ ><br>3. Star Excursion Balance Test (SEBT)Timepoint: On Day 1