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Clinical Trials/NCT04194853
NCT04194853
Completed
Not Applicable

Effects of Electromyographic Biofeedback on Performance of Vastus Medialis Oblique Muscle in Knee Osteoarthritis

Riphah International University1 site in 1 country30 target enrollmentAugust 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Riphah International University
Enrollment
30
Locations
1
Primary Endpoint
Vastus medialis Oblique(VMO) Thickness
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This study intends to determine the Effects of Electromyographic biofeedback on performance of vastus medialis oblique muscle in knee osteoarthritis.

Detailed Description

This is a single blinded randomized controlled trial, will be conducted at Railway General Hospital.Rawalpindi. (EMG) biofeedback as an adjunct therapy to standard exercise regime for increasing muscle strength ,this study is planned to determine the effects of electromyographic biofeedback on performance and thickness of vastus medialis oblique muscle, knee pain and on lower extremity function in patients with Knee Osteoarthritis. The sample size was calculated to be n=34 through Open Epi tool version 3, with 95 % confidence interval (CI), and power 80%. After the completion of therapeutic protocols, the participants will be assessed with the help of Numeric Pain Rating Scale (NPRS), WOMAC, Lequesne questionnaire , 1 Repetition maximum( RM) and with MSK ultrasound

Registry
clinicaltrials.gov
Start Date
August 1, 2019
End Date
January 8, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age : In between 45 - 65years
  • Both Genders
  • Subjects with a definite diagnosis of knee OA according to the guidelines of the American College of Rheumatology with at least 6 months of knee pain.
  • Grade 1 or 2 joint cartilage degradation based on the Kellgren-Lawrence classification
  • Body mass index (BMI) of \<35 kg/m2

Exclusion Criteria

  • Subjects who had undergone physical therapy or intraarticular injection in the past 3 months
  • Patients who had taken oral corticosteroids in the past 4 weeks
  • Patients with a history of surgical interventions on their knees
  • Subjects with a history of radiculopathy, or those with a history of systemic diseases, such as rheumatoid arthritis

Outcomes

Primary Outcomes

Vastus medialis Oblique(VMO) Thickness

Time Frame: Post 6th week

Changes from the Baseline, Musculoskeletal ultrasound will be used to measure maximum thickness of VMO muscle. Assessment will be done by a Consultant radiologist using a 7-12 MHz probe

Numeric Pain Rating Scale (NPRS)

Time Frame: Post 6 Weeks

Changes from the baseline, Numeric Pain Rating Scale (NPRS) is used to assess pain. It scores ranges from 0-10, 0 means No pain and 10 means Severe pain. Patient will be asked to verbally report the pain score.

1 Repetition Maximum

Time Frame: Post 6th week

Changes from the baseline, 1 RM Is used to assess maximum muscle strength. Patient is asked to extend knee against maximum resistance once.

Secondary Outcomes

  • Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(Post 6 weeks)

Study Sites (1)

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