- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01764620
Effects of Muscle Fatigue and a Taping Technique on Shoulder Motion of Athletes
March 30, 2013 updated by: Gisele Garcia Zanca, Universidade Federal de Sao Carlos
Effects of Muscle Fatigue and Scapular Taping on Shoulder Kinematics of Overhead Athletes
The purpose of this study is to investigate the effects of muscle fatigue in the scapular kinematics of overhead athletes with and without using a kinesio taping technique for facilitating lower trapezius function.
The hypothesis is that the taping technique could compensate for the negative effects caused by muscle fatigue in the scapular kinematics of healthy overhead athletes.
Study Overview
Status
Unknown
Conditions
Detailed Description
Muscle fatigue is a potential cause of shoulder injuries in overhead athletes.
Considering the important role of lower trapezius for functional scapular stability, it is suggested that a kinesio taping technique for facilitating its function could compensate for the negative effects of muscle fatigue on scapular kinematics.
This is a randomized crossover study and all included athletes will be evaluated in three sessions, with a period of seven days between them: Control (fatigue protocol, without taping), Kinesio Taping (fatigue protocol with elastic taping applied with tension) and Sham (fatigue protocol with taping applied without tension).
During each session, tridimensional kinematics of scapula and humerus and electromyography of serratus anterior and trapezius (upper and lower portions) muscles of dominant shoulder will be evaluated, during scaption and throwing movements, immediately before and immediately after the fatigue protocol.The changes in scapular movements (before versus after the fatigue protocol) will be compared among the sessions.
Study Type
Interventional
Enrollment (Anticipated)
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 Contact
- Name: Gisele G Zanca, MSc
- Phone Number: 55 16 33519579
- Email: gisele_gz@yahoo.com.br
Study Locations
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São Paulo
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São Carlos, São Paulo, Brazil, 13.565-905
- Recruiting
- Universidade Federal de Sao Carlos
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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 30 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Overhead athletes regularly training;
- No report of shoulder pain in the last 6 months.
Exclusion criteria:
- Previous shoulder or neck surgery;
- Previous shoulder dislocation.
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: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Control
In this session, the athletes will be evaluated before and after the fatigue protocol, without any taping application.
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Experimental: Kinesio taping
A kinesio taping technique for facilitating lower trapezius muscle function will be applied just before fatigue protocol and removed after in the end of the evaluation session.
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Sham Comparator: Sham
A similar technique, using the same tape, will be applied but without any tension (tension is considered to be the therapeutic effect).
The tape will be applied just before the fatigue protocol and removed in the end of the session.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in scapular internal/external rotations, upward/downward rotations and anterior/posterior tilt movements
Time Frame: An average of 3 minutes before and an average of 3 minutes after the fatigue protocol, in each of the 3 evaluation sessions.
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Scapular 3D kinematics will be measured during arm elevation and throwing movements, in two moments (an average of 3 minutes before and an average of 3 minutes after the fatigue protocol) in each one of the 3 sessions.
The evaluation session will have and interval of 7 days between them, and in each one the athletes will perform the fatigue protocol using either a kinesio taping application, or a sham application or without using any taping, in random order.
The changes in each session (before and after fatigue) will be compared among the sessions (without taping, with kinesio taping application and sham application).
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An average of 3 minutes before and an average of 3 minutes after the fatigue protocol, in each of the 3 evaluation sessions.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Changes in the median frequency of electromyographic signal from upper and lower trapezius and serratus anterior muscles.
Time Frame: An average of 3 minutes before and an average of 3 minutes after the fatigue protocol, in each of the 3 evaluation sessions.
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Electromyographic median frequency will be measured from upper and lower trapezius and serratus anterior muscles in order to determine muscle fatigue development and if the changes depending on the intervention used.
These assessments will be performed in two moments (an average of 3 minutes before and an average of 3 minutes after the fatigue protocol) in each one of the 3 sessions(with an interval of 7 days between them).
In each session the athletes will perform the fatigue protocol using either a kinesio taping application, or a sham application or without using any taping, in random order.The changes in each session (before and after fatigue) will be compared among the sessions (without taping, with kinesio taping application and sham).
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An average of 3 minutes before and an average of 3 minutes after the fatigue protocol, in each of the 3 evaluation sessions.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Gisele G Zanca, MSc, Universidade Federal de Sao Carlos
- Study Director: Stela M Mattiello, PhD, Universidade Federal de Sao Carlos
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
May 1, 2012
Primary Completion (Anticipated)
December 1, 2013
Study Completion (Anticipated)
July 1, 2014
Study Registration Dates
First Submitted
December 18, 2012
First Submitted That Met QC Criteria
January 7, 2013
First Posted (Estimate)
January 9, 2013
Study Record Updates
Last Update Posted (Estimate)
April 2, 2013
Last Update Submitted That Met QC Criteria
March 30, 2013
Last Verified
March 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 040/2011
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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