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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02318264
Other study ID # SUMU-PT-KTAP1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2015
Est. completion date December 2016

Study information

Verified date May 2022
Source State University of New York - Upstate Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This cross over design study will be used to determine the influence of elastic kinesiology tape on the speed and amplitude of quadriceps activation (anterior thigh) during selected resisted and weight bearing exercises.


Description:

Objective: This cross over design study will be used to determine the influence of elastic kinesiology tape on the speed and amplitude of quadriceps activation (anterior thigh) during selected resisted and weight bearing exercises. Background: Compliant tape, such as KiniseoⓇ Tape (KT), is highly elastic and claimed by the manufacturer to mimic skin. It is commonly used by physical therapists and sports medicine practitioners to treat musculoskeletal conditions and to enhance physical performance. The creators of KT teach a variety of applications techniques to affect the underlying musculature. Current theory regarding elastic tape application suggests that if the tape is applied over a muscle from the proximal to distal attachments, it will facilitate the underlying muscle while applying the tape from distal to proximal will inhibit the musculature.1 While studies have investigated the effect of elastic tape on muscle activation, few studies to date have compared the direction of application on muscle activation.2-7 Methods and Measures: Healthy subjects between 18-35 years old will be recruited from the Upstate Medical University community via email and word of mouth. Potential participants will report to the Institute for Human Performance and will be asked to complete all documentation including informed consent and a health-screening questionnaire. If eligible, qualified participants will perform 2 functional jumping exercises (vertical jump and single-leg triple hop for distance) 8 and isokinetic knee flexion and extension at 60 degrees/sec and 120 degrees/sec using the Biodex System 3 Pro Dynamometer (Biodex Medical Systems, Shirley, NY). The Biodex isokinetic machine has been shown to be a reliable and valid source of measuring peak torque, position and velocity.9 Surface electromyography (EMG) recordings will be collected from the vastus medialis and vastus lateralis during isokinetic testing. Testing will occur over four sessions. In the first session, baseline measurements and measurements immediately after KT application will be collected. In the second session, the participant will be retested after wearing the KT for up to two days (48 hours). This process will be repeated one week later during sessions three and four with KT applied in the opposite direction of the initial testing condition. KT application direction and the order of activities will be randomized for each participant.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date December 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Eligible participants were between the ages of 18 to 35 and naïve to the use of kinesiology tape. Exclusion criteria included musculoskeletal injury to the lower extremities (within the previous year), past surgery to the lower extremities, or known allergy to adhesive tape. All participants were screened for physical activity and exercise testing using the Physical Activity and Readiness Questionnaire (PAR-Q)15 (British Columbia Ministry of Health, British Columbia/Canada), resting vital signs, and American College of Sports Medicine guidelines for exercise testing. The Physical Activity and Readiness Questionnaire (PAR-Q)(British Columbia Ministry of Health) will be used as a general screen of exercise safety. Additionally, researchers will ask participants to identify possible cardiovascular and/or orthopedic risks to resistance exercise, dominant leg injuries/surgeries, and regarding history or familiarity of elastic tape. Subjects who are at risk due to recent (within the last year) musculoskeletal injury to lower extremities will be excluded from the study. Additionally, we will exclude subjects who report significant respiratory-cardiovascular disease, subjects with a history of surgery on their dominant leg, or individuals who have been trained in elastic tape theory and application. Any participant with a known allergy to adhesives will also be excluded from the study. Blood pressure and heart rate will be measured at the start of each session. Per ACSM's guidelines for exercise testing, if a participant's resting systolic blood pressure is greater than >200 mm Hg or diastolic BP is >110 mm Hg then he/she will be excluded from exercise testing and the study

Study Design


Related Conditions & MeSH terms

  • Changes Based on Duration of Tape Application
  • Direction of Kinesio Tape Application
  • Healthy Subjects

Intervention

Device:
Kinesio Tape
Elastic tape placed over the skin

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
State University of New York - Upstate Medical University

References & Publications (1)

Dolphin M, Brooks G, Calancie B, Rufa A. Does the Direction of Kinesiology Tape Application Influence Muscle Activation in Asymptomatic Individuals? Int J Sports Phys Ther. 2021 Feb 1;16(1):135-144. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Vertical Jump Height Immediately Post Tape Administration Vertical Jump Height Immediately Post Tape Administration Immediate
Primary Unilateral Three Hop for Distance Immediately Post Tape Administration Unilateral three hop for distance immediately post tape administration Immediate
Secondary EMG During Isokinetic Testing at 120 Degrees/Sec Immediately Post Tape Application EMG data were collected during the isokinetic testing at 120 degrees/sec Immediately Post Tape Application Immediate
Secondary EMG During Isokinetic Testing at 60 Degrees/Sec Immediately Post Tape Application EMG during isokinetic testing at 60 degrees/second Immediately Post Tape Application Immediate
Secondary Isokinetic Torque at 120 Degrees/Sec Immediately Post Tape Administration Isokinetic Torque at 120 Degrees/Second Immediately Post Tape Administration Immediate
Secondary Isokinetic Torque at 60 Degrees/Sec Immediately Post Tape Administration Isokinetic Torque at 60 Degrees/Second Immediately Post Tape Administration Immediate
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