Effects of Elastic Therapeutic Tapes on Performance With Healthy Subjects

September 13, 2019 updated by: Mirsad ALKAN, Bahçeşehir University

Effects of Elastic Therapeutic Tapes on Performance With Healthy Subjects: a Randomized Placebo Controlled Trial

There has been an increasing interest in Kinesiology Tape(KT) and Biomechanical Tape(BT) in clinics and athletic competitions. Recently; the performance increasing effect of taping methods on healthy subjects in sports is being investigated.

Study Overview

Detailed Description

Kinesio Taping (KT) is a technique utilizing a two way elastic tape originally created by Kenzo Kase in the 1970s. KT is a complementary method which is used as an adjunct to major therapy approaches in various musculoskeletal and neurological diseases.4 KT is employed in sports injuries and various health problems; but there is limited scientific evidence evaluating KT effectiveness and the results are inconsistent.5 One of the KT potential benefits is that of raising the range of motion through increasing blood circulation or through stimulation of cutaneous mechanoreceptors and this way it affects fascial tissue.6-8 Biomechanical Taping (BT) is a technique utilizing a four way elastic tape originally created by Ryan Kendrick in the 2010s. BT is a complementary method for supplementing load absorption, force contribution and modifying movement. BT affects tissues and movement in a mechanical way and it is almost a completely different method from KT. Kase's hypothesis is that KT affects fascial tissues and mechanoreseptors, but Kendrick's hypothesis is that BT ,which is applied in shortened position and cross joint segments, will gain potential energy in case of an extremity realized movement with antagonist activity. Then the weak agonist muscle gets activated for repositioning the extremity; this potential energy turns to kinetic energy like a released bow. As a result of kinetic energy, it may support the movement with using passive mechanical strength.9 In this study, the investigators aim to illustrate immediate effects of various taping methods on the performances of healthy subjects. In that way the investigators test hypothesis that different taping methods affect healthy subjects to improve performance. The investigators; investigate strength, active range of motion and vertical jump height as a parameters of performance with No Tape(NT), Sham Tape(ST), KT and BT.

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beşiktaş
      • İstanbul, Beşiktaş, Turkey, 34353
        • Bahçeşehir University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 24 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 18-24 BMI
  • Physically active according to International Physical Activity Questionnarie (IPAQ)

Exclusion Criteria:

  • Any known systemic diseases or medical condition
  • Sensitive or fragile skin,
  • Allergic diseases
  • Pregnancy or pregnancy suspicion
  • Using of sedative, psychosomatic or analgesic drugs

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Tests were applied with any taping.
Sham Comparator: Sham Taping
In ST stage; medical purpose, hypoallergenic OctaCare® Rigid Transparent Plaster was applied as a rigid tape. This tape is also used under rigid tapes for protecting the skin. In this study investigators didn't prefer extra rigid tape on the plaster because that was very light and less sensitive material to our knowledge so it suited our aim of placebo control.
Non-Elastic Tape
Experimental: Kinesiology Taping
In KT stage; the original Kinesio Tex® Tape Classic was applied as a kinesiology tape. In this study, investigators applied the tape with muscle activation technique and paper of tension (it was declared %10) according to Kenzo Kase's Kinesio Taping concept. It was implemented on both bileral Rectus Femoris and Calf muscles with same technique.
Tape can be elongate only one direction
Experimental: Biomechanical Taping
In BT stage; Dynamic Tape® was applied as a biomechanical tape. In this study, investigators applied the tape with offload technique and paper of tension according to Ryan Kendrick's Biomechanical Taping concept. It was implemented on both bileral Rectus Femoris and Calf muscles with same technique.
Tape can be elongate only two direction

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Vertical Jump With Each Taping Application
Time Frame: baseline, and immediate effect in a 15 minutes
A fotoelectrical sensor base "Micro Gate Opto Jump Next®, software version 1.10, BFS Vertical Jump protocol with three jumps" was used for quantitative analysis of Counter Movement Vertical Jump (CMVJ). Minimum, maximum and average values of jumping height for all jumps (10) were recorded as canti-meter (cm).
baseline, and immediate effect in a 15 minutes
Change From Muscle Strength With Each Taping Application
Time Frame: baseline, and immediate effect in a 15 minutes
A hand held electronic dynamometer "MicroFet® 2" was used to evaluate isometric bilateral knee extension and ankle dorsal flexion strength.11 Measurements were repeated three times and maximum value of strength was recorded as Kilogram-Force (Kg-F).
baseline, and immediate effect in a 15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change From Active Range Of Motion With Each Taping Application
Time Frame: baseline, and immediate effect in a 15 minutes
A wide angle webcam "logitech® c920 full hd pro web cam" that was integrated with opto jump software was used for assessment of active range of motion in front of jumping on image based assessment tool of opto jump software. Acromion, Trochantor major of femur, lateral epicondyle of femur, Lateral Condyle of Tibia and medial malleolus of tibia were marked for the indicator before the jumps. Videos, recorded at the same time with jump and synchronous with jumping values, were used for resolving knee and hip flexion degrees before jump with maximum height and they were assessed with indicators on computer surface on optojump software. Values recorded as degrees (º).
baseline, and immediate effect in a 15 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Habibe Serap İnal, Bahçeşehir University
  • Principal Investigator: Şebnem Nur Alkan, Bahçeşehir University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 3, 2016

Primary Completion (Actual)

January 12, 2017

Study Completion (Actual)

January 12, 2017

Study Registration Dates

First Submitted

August 29, 2019

First Submitted That Met QC Criteria

September 13, 2019

First Posted (Actual)

September 16, 2019

Study Record Updates

Last Update Posted (Actual)

September 16, 2019

Last Update Submitted That Met QC Criteria

September 13, 2019

Last Verified

September 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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