Effects of Kinesio Tape on Delayed Onset Muscle Soreness

  • STATUS
    Recruiting
  • End date
    Jan 30, 2023
  • participants needed
    36
  • sponsor
    Indiana University
Updated on 22 March 2022
Accepts healthy volunteers

Summary

The purpose of this study is to determine the effect of Kinesio tape on delayed onset muscle soreness of the biceps muscle of your arm following strenuous exercise of the bicep muscle.

Description

Participants will complete 4 testing sessions that will be held on 4 separate days (Baseline, Eccentric Exercise day, 48 hours post exercise, and 72 hours post exercise). All sessions will take place in the National Institute of Fitness and Sport, where the Department of Kinesiology laboratories are located.

During the first session (Baseline), the purpose and procedures of the research will be explained by the investigator, co-investigator, or a research assistant in more detail. Participants will read and sign the informed consent form and then undergo an exclusion/inclusion criteria assessment which includes the Physical Activity Readiness Questionnaire (PAR-Q), and brief questionnaire. All study personnel/staff obtaining informed consent will be trained in the responsible conduct of research. All participants will be asked if they have a known allergy to Kinesio Tape (KT) or if they have sensitive skin. Those with sensitive skin will be administered an allergy test. After screening and enrollment, participants will complete baseline assessments of muscle pain and function, pain sensitivity, and psychological risk factors (See outcome measures).

During Session 2, strength of the non-dominant bicep will be measured first. Participants will then perform an eccentric exercise protocol designed to induce delayed onset muscle soreness (DOMS) on the non-dominant arm. Strength of the non-dominant bicep will be measured immediately post the eccentric exercise protocol. At the end of this session, subjects will be randomly assigned to one of two intervention groups (experimental KT group, placebo KT group) or a control group (i.e., no intervention performed). The experimental group will receive KT with proper technique and tension (10-20%), while the placebo group will receive KT without technique and tension.

Sessions 3 and 4 will occur approximately 48 and 72 hours post Session 2, respectively. All the outcome variables will be measured during these sessions. For participants in the KT groups, the tape will be removed at the end of session 4, as described below.

Details
Condition Delayed Onset Muscle Soreness
Treatment kinesiotape
Clinical Study IdentifierNCT04128670
SponsorIndiana University
Last Modified on22 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

to 30 years old

Exclusion Criteria

Participating in any strengthening exercises or activities of the upper extremities for the past month
Regularly (~2x per month) participating in strengthening exercises or activities that include lengthening actions of the upper extremity for the past 6 months
An answer of yes to any of the seven questions on the first page of the 2019 Physical Activity Readiness Questionnaire [PAR-Q: 16] indicating that the subject is not physically ready for exercise without a medical exam. These exclusions include the
following
If participant's doctor has ever said that he/she has a heart condition or high blood pressure
Pain in chest at rest, during daily activities of living, or when doing physical activity
If participant has ever lost balance because of dizziness or has lost consciousness in the past 12 months
If the participant currently has (or have had within the past 12 months) a bone, joint, or soft tissue (muscle, ligament, or tendon) problem that could be made worse by becoming more physically activity
If participant is currently taking prescribed medications for a chronic medical condition
If the participant's doctor has ever told them that they should only do medically supervised physical activity
Currently taking nutritional supplements or anti-inflammatory medication on a daily
Any injury or surgery to the neck or upper extremity in the past 6 months
basis
Open or scabbed wounds in the arm area to be taped
Known allergies to the tape or medical adhesive bandages
If skin irritation develops to the tape
Session exclusion criteria
● Taking over-the-counter pain medications on days of testing, prior to testing sessions
including acetaminophen (Tylenol) and nonsteroidal inflammatory drugs (NSAIDs), including
ibuprofen (Motrin, Advil) or naproxen (Aleve, Naprosyn)
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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