The Effectiveness of Kinesio® Tex Tape on Gluteus Medius Activation in Dancers

December 12, 2017 updated by: NYU Langone Health
The purpose of this research is to determine if a specific type of elasticated athletic tape (Kinesio Tex Tape) increases muscle activation among professional level dancers. Investigators will determine if changes in muscle activation with the elasticated tape differ from changes experienced with no tape and/or sham tape, and if it coincides with subjective sense of muscle activation.

Study Overview

Status

Withdrawn

Intervention / Treatment

Study Type

Interventional

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

    • New York
      • New York, New York, United States, 10016
        • New York University School of Medicine

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 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Uninjured professional level dancers

Exclusion Criteria:

  • Non-professional level of dance or non-dancer; obesity (body mass index greater than 30 kg/m²)
  • A history of major back, abdominal, or lower extremity surgery
  • A history of muscle diseases; a history of serious cardiovascular diseases (e.g., cardiac insufficiency, arrhythmia, severe hypertension, vascular insufficiency)
  • A history of serious respiratory diseases; major fractures of the lower extremities; lower extremity or trunk injury within the last year; a history of surgery within the last year, a history of stroke, acute, or chronic infections; serious metabolic diseases
  • Glaucoma
  • Structural disease or severe congenital deformities of the spine of a high degree
  • Inguinal, femoral, or umbilical hernia; or diseases related to body equilibrium.

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: K Tape Group
The airplane test requires the subject to bend forward, bringing the upper body and one leg horizontal, making a "T" position with the body with the arms out to the sides while in single-leg stance; they then bend the supporting leg, bringing the finger tips towards the floor, followed by straightening the supporting leg and bringing the arms back out to the sides. This motion is repeated five times on each leg per trial. The airplane will be performed to a metronome to standardize performance time
Active Comparator: Sham Group
The airplane test requires the subject to bend forward, bringing the upper body and one leg horizontal, making a "T" position with the body with the arms out to the sides while in single-leg stance; they then bend the supporting leg, bringing the finger tips towards the floor, followed by straightening the supporting leg and bringing the arms back out to the sides. This motion is repeated five times on each leg per trial. The airplane will be performed to a metronome to standardize performance time
Experimental: No Tape
The airplane test requires the subject to bend forward, bringing the upper body and one leg horizontal, making a "T" position with the body with the arms out to the sides while in single-leg stance; they then bend the supporting leg, bringing the finger tips towards the floor, followed by straightening the supporting leg and bringing the arms back out to the sides. This motion is repeated five times on each leg per trial. The airplane will be performed to a metronome to standardize performance time

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change in Muscle Activity measured via electromyography
Time Frame: Baseline and 1.5 hours
Baseline and 1.5 hours

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Donald Rose, MD, New York University Medical School

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)

January 1, 2017

Primary Completion (Actual)

December 1, 2017

Study Completion (Actual)

December 1, 2017

Study Registration Dates

First Submitted

April 13, 2016

First Submitted That Met QC Criteria

April 15, 2016

First Posted (Estimate)

April 18, 2016

Study Record Updates

Last Update Posted (Actual)

December 14, 2017

Last Update Submitted That Met QC Criteria

December 12, 2017

Last Verified

December 1, 2017

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 15-00705

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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.

Clinical Trials on Gluteus Medius Activation

Clinical Trials on Airplane Test

3
Subscribe