The Instant Effect of Kinesiology Taping in Patients With Knee OA

August 4, 2022 updated by: Aylin Ataş, Kırıkkale University

Investigation of the Instant Effect of Kinesiology Taping on Rectus Femoris Muscle on Muscle Activation, Physical Performance and Proprioception in Knee Osteoarthritis Patients

The aim of this study is to determine instant effect of kinesiology taping applied to the rectus femoris on muscle activation, physical performance and proprioception in patients with knee osteoarthritis.

Study Overview

Status

Completed

Detailed Description

40 patients with knee OA will be included in the study. Intervention group and placebo group will be formed. Facilitation taping will be applied on the rectus femoris of the patients in the taping group. The patients in the placebo group will be placed tape on the rectus femoris without any tension. Muscle activation, physical performance and proprioception will be evaluated before taping and 30 minutes after taping.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kırıkkale, Turkey
        • Kırıkkale University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

45 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients aged 45-65 years,
  • Patients with independent ambulation,
  • Patients with Grade II-III knee osteoarthritis according to the Kellgren and Lawrence Classification,
  • Patients not using NSAIDs during the study,
  • Patients who volunteered to participate in the study

Exclusion Criteria:

  • Patients with previous surgery on the lower extremities
  • Patients with neuromuscular disease
  • Patients with vestibular pathology
  • Patients with diseases of the cardiopulmonary system,
  • Patients with communication difficulties,
  • Patients who have received physiotherapy or intra-articular injections in the last 6 months or who exercise

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: taping group
Facilitation taping will be applied to the rectus femoris of patients with knee OA in the taping group.
The tape will be fixed without any tension 10 cm below the origin of the rectus femoris muscle. Then 35-50% tension will be applied to the band and descended to the patella. After this point, the Y-shaped band will be terminated to wrap the patella medially and laterally without any tension.
PLACEBO_COMPARATOR: placebo group
The patients with knee OA in the placebo group will be placed tape on the rectus femoris without any tension.
The tape will attach to the rectus femoris without any tension.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
muscle activation
Time Frame: 5 minutes
The muscular activation of the Rectus Femoris will be measured with the EMG (Euro Track MyoPlus 4) device before and after the taping application. With the patient in the sitting position with the hip and knee flexed to 90 degrees, active electrodes will be placed on the motor point of the muscle, three measurements will be made, and the highest MVIC value will be recorded.
5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
timed up and go test
Time Frame: 5 minutes
Individuals will be asked to get up while sitting on the chair, walk three meters, return from the marked point at the end of three meters, walk towards the chair again and sit on the chair. The time taken for the individual's performances will be recorded in seconds.
5 minutes
5 times sit-to-stand test
Time Frame: 1 minutes
Patients will be asked to stand up and sit down fully upright from the chair with armrests as quickly as possible five times, and the elapsed time will be recorded.
1 minutes
proprioception
Time Frame: 5 minutes
Participants will sit on a chair with 90° knee flexion. The lower extremities of the participants will be passively and randomly moved from 90° knee flexion to each of the 15°, 30° and 45° angles. After holding the lower extremity at each target angle for 10 seconds, return to the starting position. After waiting 10 seconds in the starting position, the participants will bring their knees to the target angle on their own and stop. Accordingly, the absolute value of the participant's deviation from the target angle will be measured three times for each target angle with the help of a goniometer and the average value will be calculated.
5 minutes
WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index)
Time Frame: 5 minutes
It consists of three parts and 24 questions in which pain, stiffness and physical function are questioned. The maximum scores that can be obtained from the index are 20 for the pain subgroup, 8 for stiffness, and 68 for physical function. High scores indicate increased pain and stiffness and impaired physical function.
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Aylin ATAŞ, Kırıkkale University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

September 6, 2021

Primary Completion (ACTUAL)

June 27, 2022

Study Completion (ACTUAL)

June 27, 2022

Study Registration Dates

First Submitted

December 3, 2021

First Submitted That Met QC Criteria

December 3, 2021

First Posted (ACTUAL)

December 16, 2021

Study Record Updates

Last Update Posted (ACTUAL)

August 8, 2022

Last Update Submitted That Met QC Criteria

August 4, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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