A Comparison of Kinesio® Taping Methods for Subjects With Patellar Tendonitis

Overview

The purpose of this study is to explore the possible effects Kinesio Tape may have on proprioception in individuals with patellar tendonitis. A supportive knee application, a facilitative hip application, and a combination of the two will be applied and compared. Within and between group comparisons will be drawn.

Participants will report for two research sessions with 24-36 hours between. Prior to arrival, they will complete a digital Victorian Institute of Sport Assessment for Patellar Tendonitis (VISA-P) and email it to the researcher. Participants must score less than 80 (out of a possible 100) to be considered for this study. If the individual meets the inclusion criteria, he/she will be scheduled for the 1st session. Upon arrival to the first session, informed consent will be obtained, the VISA-P will be reviewed, and intance of patellar tendonitis will be confirmed through palpation. Participants will then completed a Tampa Scale for Kinesiophobia (TSK) to measure fear of movement and a Visual Analog Scale (VAS) to measure overall pain. Height and weight measurments will be taken due to requirements of the Biodex Balance System (BBS), which will be used for balance measurements. Participants will take two, twenty-second practice tests, one with eyes open and one with eyes closed, followed by two minutes rest. Baseline testing will then be completed as follows: the participant will complete two tests with eyes open, and two tests with eyes closed on the injured leg, each with one minute rest between. The participant will then be taped with Kinesio Tape to either the hip, knee, or both the hip and knee according to the random group assignment. They will then rest for 15 minutes and complete a second round of balance testing with the same parameters as baseline testing. Participants will be scheduled for a second day no less that 24 hours and no more than 36 hours for re-test purposes.

On the second day of testing, participants will be given $10 for their participation on Day 1. If they want to continue with testing procedures, they will participate in the same balance testing procedures as Day 1. The integrety of the tape application will be confirmed, and second TSK and VAS scale will be administered. A final round of balance testing will be completed, and the participant will receive an additional $10 if they choose to complete both days of testing.

This research will allow us to compare results of the TSK, the VAS and the BBS testing both within subject and between group.

Full Title of Study: “A Comparison of Kinesio® Taping Methods for Subjects With Patellar Tendonitis”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: May 2020

Interventions

  • Other: Kinesio Tape
    • Kinesio Tape will be applied to treat the pain associated with patellar tendonitis, to treat the cause of the pain, and to treat both factors.

Arms, Groups and Cohorts

  • Experimental: Hip
    • Gluteus medius facilitation tape
  • Experimental: Knee
    • Patellar sling tape
  • Experimental: Hip and Knee
    • Gluteus medius facilitation and patellar sling tape

Clinical Trial Outcome Measures

Primary Measures

  • Tampa Scale for Kinesiophobia
    • Time Frame: 24 hours
    • Measures fear of movement, score range 17-68, higher score means higher degree of kinesiophobia
  • Visual Analog Scale
    • Time Frame: 24 hours
    • Measures overall pain, score range 1-10, higher score indicates more pain
  • Biodex Balance System
    • Time Frame: 24 hours
    • Measures balance

Participating in This Clinical Trial

Inclusion Criteria

  • score of less than 80 on the Victorian Institute of Sport Assessment for Patellar Tendonitis (VISA-P)
  • experienced patellar tendon pain for greater than 14 days
  • tender to palpation at the patellar tendon.

Exclusion Criteria

  • knee surgery in the last six months
  • acute injury to the knee
  • any pain in the ankles, hips or core that may compromise balance testing
  • any allergy to adhesive
  • malignancies
  • cellulitis
  • skin infection
  • diabetes
  • fragile skin

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 50 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • North Dakota State University
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Contact(s)
    • Katie Lyman, PhD, 701-231-8208, katie.lyman@ndsu.edu

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