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Clinical Trials/NCT04019366
NCT04019366
Completed
N/A

Effects of Balance Training Using Biodex Stability System in Patients With Symptomatic Knee Osteoarthritis.

Riphah International University1 site in 1 country43 target enrollmentFebruary 1, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Riphah International University
Enrollment
43
Locations
1
Primary Endpoint
Time up and Go test (TUG)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This was a randomized control Trial, conducted with two group of patients, one has received Balance and stability training on Biodex stability system along with conservative protocol of traditional exercises. the other group has received only conservative protocol of traditional exercises

Detailed Description

Patients with Symptomatic Knee Osteoarthritis have balance and stability deficits. In routine such patients are not evaluated and treated on balance and stability parameters. So this study was conducted with objectives to determine the effects of Balance training using Biodex stability system in patients with symptomatic knee osteoarthritis. Experimental group has received Balance and stability training on Biodex stability system along with conservative protocol of traditional exercises. Control group has received only conservative protocol of traditional exercises.

Registry
clinicaltrials.gov
Start Date
February 1, 2018
End Date
June 30, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Bilateral knee pain
  • Age 35-65, Both genders
  • Grade 2 or 3 on Kellgren classification for Knee Arthritis

Exclusion Criteria

  • Past history of total knee artthroplasty
  • Intra articular steroid injection
  • Rheumatoid Arthritis
  • Use of Assistive devices e.g. canes, walkers and braces
  • Knee injury

Outcomes

Primary Outcomes

Time up and Go test (TUG)

Time Frame: Post 4th Week

Patients were asked to perform test at usual walking speed. Initial testing standardized verbal instructions given to the participant regarding procedure. For performing TUG participants were instructed to walk three meter and then, walk back to sit down. Note time on stopwatch. The average of tests trail was measured as the mean of TUG.

overall stability index (OSI)

Time Frame: Post 4th Week

Measures were obtained from 20-sec trials during which participants were asked to maintain an upright standing position on their dominant limb on the unstable surface of the Biodex Stability and Balance System.Its reliability is R = .94

Anterior-posterior stability index (APSI)

Time Frame: Post 4th Week

Measures were obtained from 20-sec trials during which participants were asked to maintain an upright standing position on their dominant limb on the unstable surface of the Biodex Stability and Balance System.Its reliability is R = .95

Medial-lateral stability index (MLSI)

Time Frame: Post 4th Week

Measures were obtained from 20-sec trials during which participants were asked to maintain an upright standing position on their dominant limb on the unstable surface of the Biodex Stability and Balance System.Its reliability is R = .93

Secondary Outcomes

  • Numeric Pain Rating Scale (NPRS)(post 4th week)
  • Western Ontario and McMaster Universities Arthritis Index (WOMAC)(Post 4th week)

Study Sites (1)

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