The Effects of Kinesio Taping on Pain, Range of Motion, and Functional Performance in People With Knee Osteoarthritis

May 25, 2024 updated by: Marwan Mahmoud Aljohani, Taibah University

The Effects of Kinesio Taping on Knee Pain, Range of Motion, and Functional Performance in People With Knee Osteoarthritis

The goal of this clinical trial is to evaluate the effectiveness of Kinesio Taping in individuals with knee osteoarthritis (KOA). KOA is a common condition that can lead to pain, stiffness, and decreased mobility. The main questions it aims to answer are:

  • Does Kinesio Taping reduce pain in individuals with KOA?
  • Can Kinesio Taping improve the range of motion and functional performance in those suffering from KOA?

Participants will be asked to:

Attend assessment sessions at the outpatient Physical Therapy clinic at Taibah University.

Undergo Kinesio Taping three times over 12 days. Complete specific physical tests and questionnaires before and after the intervention period to measure their pain and mobility.

Researchers will compare the group that receives Kinesio Taping with the group that receives sham (placebo) taping to see if there are significant differences in pain reduction and improvements in movement and daily function.

Study Overview

Status

Completed

Conditions

Detailed Description

Study Overview

This clinical trial explores Kinesio Taping's (KT) effect on knee osteoarthritis (KOA) in adults. It delves into whether KT can alleviate pain and improve joint movement and daily functioning. The research, hosted at Taibah University's Physical Therapy clinic, focuses on practical benefits for patients with KOA, a condition that leads to significant discomfort and mobility issues, especially prevalent in Saudi Arabia.

Study Design

In a randomized and single-blinded approach, participants are divided into two groups. One group receives actual Kinesio taping, while the other undergoes a sham procedure, with neither group aware of their specific treatment type to ensure unbiased results.

Intervention Procedures

Participants undergo three Kinesio taping sessions spread over 12 days. The taping technique is performed according to prescribed methods that target the quadriceps femoris muscle, believed to influence pain perception and joint function positively.

The study employs a before-and-after intervention assessment model. Initial data collection includes patients' demographic details and baseline characteristics related to their health status and disease severity. Following the intervention, the same measures are reassessed to evaluate any changes attributed to the KT.

Study Type

Interventional

Enrollment (Actual)

29

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

      • Medina, Saudi Arabia, 42353
        • Taibah 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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients clinically and radiologically diagnosed with unilateral or bilateral knee OA.
  • Independent gait
  • Any grade on the Kellgren-Lawrence scale

Exclusion Criteria:

  • Previous fractures of the femur and/or tibia.
  • Comorbidities such as neurological diseases, malnutrition, and other inflammatory and/or infectious diseases.
  • Radicular pain in the lower limbs or diabetic neuritis.
  • Prior physiotherapy in the past month.

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 Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Sham Comparator: Sham group
Sham taping will be applied horizontally across the muscle fibers without any stretching. the tape here will be applied transverse to the quadriceps femoris muscle. The patients will be in a supine position with their hips flexed at 30 degrees and their knees flexed at 60 degrees.
Experimental: Kineso taping group
This group will receive the tape on their quadriceps femoris muscle. First, the tape will be cut in a Y-shaped Kinesio type and then applied over the quadriceps femoris muscle. The tape will be applied at a point of 5 cm inferior to the anterior superior iliac spine to the patella (origin to insertion), with the patient in a supine position with 25% tension on the tape. Then, each patient will flex his or her knee, and the Y-shaped tape (the end of the tape) will be circled around the patella, ending at its inferior side with no tension.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain (Visual analog scale)
Time Frame: At baseline (pre-intervention), and then repeated immediately after the intervention
a tool that measures pain intensity. It consists of a straight line, typically 10 cm long, with "no pain" on one end and "severe pain" on the other. Participants mark a point on the line that represents their current level of pain, providing a quantitative measure of pain intensity.
At baseline (pre-intervention), and then repeated immediately after the intervention
Knee range of motion
Time Frame: At baseline (pre-intervention), and then repeated immediately after the intervention
the knee range of motion measured by goniometer
At baseline (pre-intervention), and then repeated immediately after the intervention
Timed up and go test
Time Frame: At baseline (pre-intervention), and then repeated immediately after the intervention
measures mobility by timing how long it takes a person to stand up from a chair, walk 3 meters, turn around, walk back, and sit down. Longer times suggest decreased mobility and a higher fall risk.
At baseline (pre-intervention), and then repeated immediately after the intervention
The 50-foot Walk
Time Frame: At baseline (pre-intervention), and then repeated immediately after the intervention
measures walking speed over a short distance. Participants walk 50 feet as quickly and safely as possible, and the time taken is recorded. This test assesses functional mobility and endurance.
At baseline (pre-intervention), and then repeated immediately after the intervention
Knee Osteoarthritis Outcome Score (KOOS)
Time Frame: At baseline (pre-intervention), and then repeated immediately after the intervention
is a patient-reported questionnaire developed to assess the patient's opinion about their knee and associated problems. It consists of five subscales: Pain, Other Symptoms, Function in daily living (ADL), Function in Sport and Recreation (Sport/Rec), and knee-related Quality of Life (QOL). The scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems. It is widely used in the assessment of the short-term and long-term consequences of knee osteoarthritis.
At baseline (pre-intervention), and then repeated immediately after the intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Marwan MA Aljohani, Phd, Taibah University

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)

March 1, 2024

Primary Completion (Actual)

April 30, 2024

Study Completion (Actual)

May 9, 2024

Study Registration Dates

First Submitted

March 12, 2024

First Submitted That Met QC Criteria

March 20, 2024

First Posted (Actual)

March 25, 2024

Study Record Updates

Last Update Posted (Actual)

May 29, 2024

Last Update Submitted That Met QC Criteria

May 25, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • TUMRHS

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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