- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06289218
Kinesio Taping Versus Interferential Current Therapy in Treating Knee Osteoarthritis
Kinesio Taping Versus Interferential Current Therapy in Treating Knee Osteoarthritis: a Comparative Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Knee osteoarthritis (KOA) is the most common form of degenerative joint disease affecting 15%-40% of people over 40 years of age. In 2020, the global incidence of KOA was 86.7 million individuals. KOA is responsible for substantial health and economic costs. KOA is the most common cause of pain and disability among older persons. The key symptoms of KOA are pain, functional disability, and decreased patient quality of life through its negative effects on mobility, mood, and sleep. Other symptoms are swelling, stiffness, joint deformity, and muscular atrophy.
The Treatment goals for KOA are to decrease pain and improve physical function. Physical therapy decreased pain and functional disability in patients with KOA. The therapeutic techniques include therapeutic exercises, electrotherapy, and manual therapy. Several meta-analysis and systematic reviews have evidence of various types of exercises including aerobic and resistance exercises which is effective in reducing pain and functional disabilities in a patient with KOA especially quadriceps muscle strengthening with open and closed chain training. Specific recommendations including physical activity, reducing body weight, reducing sedentary time, and managing diabetes disease can improve function and symptoms of KOA. To improve the individual's function, and reduce pain and disability, several interventions had been investigated to promote physical activity.
Kinesio taping (KT) is a conservative therapeutic technique used for the treatment of several musculoskeletal disorders which has increased attention from physicians and physiotherapists in recent years. KT, first introduced in 1979 in Japan, is used for the treatment and prevention of several sports injuries and several clinical conditions. In 2011, KT is recommended by the American College of Rheumatology (ACR) for the treatment of patients with knee OA, and it is commonly used to treat knee OA.
Kinesio taping (KT) is an alternative taping technique which is an elastic woven cotton strip with heat-sensitive acrylic adhesive, a high-stretch elastic adhesive material, it is applied directly to the skin and can be left on the skin for several days due to its strong adherence. The application of KT for four weeks can reduce the pain so the patient can reduce the use pain killers. Kinesio taping (KT) is a low-cost, safe, noninvasive, non-pharmacological method, that has minimal side effects and can be a convenient option for the treatment of musculoskeletal disorders such as knee OA.
Interferential current (IFC) is a simple, non-invasive, non-pharmacological, more comfortable treatment used to relieve pain. IFC known as kilohertz-frequency alternating current, which is a pair of signal generators with one fixed frequency of 4000 Hz and the other varying in frequency between 4000 and 4250 Hz. IFC can reduce skin impedance, reach deeper tissue, and can be utilized as an alternative medication or supplement to drugs in treating pain. IFC is the most effective pain relief treatment for the management of KOA.
Exercises play a major role in treating patients with KOA; it can improve both pain and function. Therefore What about comparing the application of kinesio taping combined with exercises versus the IFC therapy combined with exercises in treating patients with KOA?
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Nourhan Elsaid Ahmed Elsaid
- Phone Number: 966540792567
- Email: nourhanelsaid1993@gmail.com
Study Contact Backup
- Name: Marihan Zakaria Aziz Makary, Dr
- Phone Number: 01201227971
- Email: marihan_aziz@cu.edu.eg
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Forty-eight Male and female patients aged between 40 and 65 years old were diagnosed clinically and radiologically as knee osteoarthritis grade mild and moderate chronic knee osteoarthritis.
- BMI ranges between 20 and 32 kg/m2.
- Knee OA grades 1 and 2 are based on Kellgren and Lawrence's grades. Narrowing of joint space, definite osteophytes.
- Unilateral knee osteoarthritis.
Knee pain for most days of the prior month, in addition to at least 3 of the following:
- Crepitus on active joint motion
- Morning stiffness less than 30 minutes duration
- Age older than 50 years
- Bony enlargement of the knee on examination
- Bony tenderness of the knee on examination
- No palpable warmth.
Exclusion Criteria:
Patients having the following conditions will be excluded from the study:
- Comorbidities such as (rheumatoid arthritis, cancer, osteoporosis, and joint infection).
- Previous surgery for knee OA.
- BMI more than 33 kg/m2.
- Suffering from polyarticular disease.
- Severe mechanical deformity (diaphyseal Varus deformity of 4° and valgus of 16°).
- Previous arthroscopy within the last year.
- Systemic autoimmune rheumatoid disease (connective tissue disease and systemic necrotizing vasculitis).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Control group
|
exercise only
|
Experimental: interferential current plus exercise
interferential current plus exercise group
|
IFC plus exercise
Other Names:
|
Experimental: kinesio taping plus exercise
kinesio taping plus exercise group
|
KT plus exercise
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
knee flexion range of motion
Time Frame: pre-intervention and after 4 weeks of treatment
|
to measure Knee joint active range of motion (flexion) by universal goniometer
|
pre-intervention and after 4 weeks of treatment
|
knee extension range of motion
Time Frame: pre-intervention and after 4 weeks of treatment
|
to measure Knee joint active range of motion (extension) by universal goniometer
|
pre-intervention and after 4 weeks of treatment
|
quadriceps muscle strength
Time Frame: pre-intervention and after 4 weeks of treatment
|
to test the isometric quadriceps muscle strength by hand-held dynamometer
|
pre-intervention and after 4 weeks of treatment
|
The Western Ontario and McMaster Universities Osteoarthritis Index
Time Frame: pre-intervention and after 4 weeks of treatment
|
to measure knee function and knee pain degree
|
pre-intervention and after 4 weeks of treatment
|
Timed up and go test
Time Frame: pre-intervention and after 4 weeks of treatment
|
to measure knee function mobility by the Timed up and go test
|
pre-intervention and after 4 weeks of treatment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Salwa Fadl Abd Elmageed, Prof.Dr, Professor at Department of Physical Therapy for Musculoskeletal Disorders and Its Surgery
Publications and helpful links
General Publications
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- Katz JN, Arant KR, Loeser RF. Diagnosis and Treatment of Hip and Knee Osteoarthritis: A Review. JAMA. 2021 Feb 9;325(6):568-578. doi: 10.1001/jama.2020.22171.
- Lu Z, Li X, Chen R, Guo C. Kinesio taping improves pain and function in patients with knee osteoarthritis: A meta-analysis of randomized controlled trials. Int J Surg. 2018 Nov;59:27-35. doi: 10.1016/j.ijsu.2018.09.015. Epub 2018 Sep 28.
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Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Treating knee osteoarthritis
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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