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

NCT ID: NCT06327243

Last Updated: 2024-05-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

29 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-03-01

Study Completion Date

2024-05-09

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Knee Osteoarthritis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
Participants will not know if they are receiving the actual Kinesio Taping (KT) treatment or a sham taping. The KT will be applied following the correct standards for the rectus femoris muscle, including appropriate stretching. Conversely, the placebo taping will be applied horizontally across the muscle fibers without any stretching. The therapists applying the tape will know which treatment each participant is allocated to ensure that the application of either the real KT or the placebo taping aligns with the study's protocol.

Study Groups

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Kineso taping group

Group Type EXPERIMENTAL

Elastic tape ( kinesio tape)

Intervention Type OTHER

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.

Sham group

Group Type SHAM_COMPARATOR

Sham Taping

Intervention Type OTHER

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.

Interventions

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Elastic tape ( kinesio tape)

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.

Intervention Type OTHER

Sham Taping

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.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

40 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Taibah University

OTHER

Sponsor Role lead

Responsible Party

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Marwan Mahmoud Aljohani

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Marwan MA Aljohani, Phd

Role: PRINCIPAL_INVESTIGATOR

Taibah University

Locations

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Taibah University

Madinah, , Saudi Arabia

Site Status

Countries

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Saudi Arabia

Other Identifiers

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TUMRHS

Identifier Type: -

Identifier Source: org_study_id

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