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Clinical Trials/NCT05351996
NCT05351996
Completed
Not Applicable

Does Kinesiotaping Effective for Knee Osteoarthritis? Randomized Controlled Trial

Bozyaka Training and Research Hospital1 site in 1 country57 target enrollmentNovember 20, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis, Knee
Sponsor
Bozyaka Training and Research Hospital
Enrollment
57
Locations
1
Primary Endpoint
Change from Baseline Pain intensity-rest at 1st hour, 3rd week, and 7th week
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Kinesiotape is one of the treatment choices for the patients with knee osteoarthritis. Unlike the brace, it seems to be an important advantage in kinesiotape application in that it permits the movement of the joint. However, kinesiotape is conditionally recommended for knee osteoarthritis in the 2019 American College of Rheumatology treatment recommendations due to limiting the quality of evidence, using various application methods, and the lack of blindness concerning its use is not possible.

The aim of the study is to determine the effects of kinesiotaping on pain, physical performance, knee range of motion, and postural stability in knee osteoarthritis.

Detailed Description

Non-pharmacological treatments are recommended as first-line management in knee osteoarthritis. Kinesiotape was regarded as a supplementary intervention for patients with knee osteoarthritis. Although the results are conflicting, regarding knee osteoarthritis, recently published studies indicate beneficial effects of kinesiotape on knee-related health status, pain, quadriceps muscle strength, and range of motion. On the other hand, the measurements were performed immediately following taping or within a short-term period. The inconsistency of the study data still indicates that the efficacy of kinesiotape in knee osteoarthritis should be evaluated in randomized controlled trials. Therefore a study that investigates both short and long-term follow-up results are warranted. This study aimed to determine the immediate and long-term effects of the single and repetitive application of kinesiotape on pain, knee joint range of motion, postural stability, and physical performance in participants with knee osteoarthritis. The results of this study will support evidence-based reports based on the effectiveness of kinesiotape in knee osteoarthritis and recommendations for future studies.

Registry
clinicaltrials.gov
Start Date
November 20, 2019
End Date
October 26, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Bozyaka Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Şeniz Akçay

University of Health Sciences Bozyaka Training and Research Hospital Physical Medicine and Rehabilitation Department, Assoc. Prof.

Bozyaka Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Pain for a minimum of 3 months
  • Pain intensity within the last week minimum of 3 according to the visual analogue scale (VAS) at the symptomatic knee
  • Grade 2-3 knee OA according to the Kellgren and Lawrence Scale
  • Ability to perform the tests

Exclusion Criteria

  • Fragile, very sensitive skin, or lesions in the area
  • Inflammatory arthritis
  • Inability to perform functional tests
  • Pregnancy
  • Use of drugs associated with a psychiatric disorder
  • Previous joint replacement surgery for knee/hip joints
  • Diagnosis with balance disorder
  • Disorders that may cause loss of muscle strength in the lower extremities
  • Previous experience with the Kinesiotaping method

Outcomes

Primary Outcomes

Change from Baseline Pain intensity-rest at 1st hour, 3rd week, and 7th week

Time Frame: Baseline (week 0), 1st hour, 3rd week, 7th week

Pain intensity was assessed by using the Visual Analogue Scale (VAS). Each patient was asked to indicate pain intensity during rest at each assessment point (on a 0-10 points numerical pain rating scale; higher scores indicate severe pain).

Change from Baseline Pain intensity-activity at 1st hour, 3rd week, and 7th week

Time Frame: Baseline (week 0), 1st hour, 3rd week , 7th week

Pain intensity was assessed by using the Visual Analogue Scale (VAS). Each patient was asked to indicate pain intensity during 50-meter walking test at each assessment point (on a 0-10 points numerical pain rating scale; higher scores indicate severe pain).

Secondary Outcomes

  • Change from Baseline Knee-Related Health Status at 1st hour, 3rd week, and 7th week(Baseline (week 0), 1st hour, 3rd week , 7th week)
  • Change from Baseline Pain-free Knee Range of Motion at 1st hour, 3rd week, and 7th week(Baseline (week 0), 1st hour, 3rd week , 7th week)
  • Change from Baseline Physical Function at 1st hour, 3rd week, and 7th week(Baseline (week 0), 1st hour, 3rd week , 7th week)
  • Change from Baseline Static Postural Stability at 1st hour, 3rd week, and 7th week(Baseline (week 0), 1st hour, 3rd week , 7th week)
  • Change from Baseline Dynamic Postural Stability at 1st hour, 3rd week, and 7th week(Baseline (week 0), 1st hour, 3rd week , 7th week)

Study Sites (1)

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