- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04078945
Risk Factors of Shoulder Injuries in Youth Volleyball Players
Risk Factors of Shoulder Injuries in Youth Volleyball Players : Prospective Study
Study Overview
Status
Conditions
Detailed Description
About 100 youth volleyball players (13-20 years), playing at least 8 hours volleyball in a week will be included in the study.
At the beginning of the 2019-2020 season, they will have to take part at the following evaluations :
Clinical evaluation :
- Scapular dyskinesis assessment (normal, subtle abnormality and obvious abnormality)
- Scapular upward rotation at 0°, 45°,90° and 120° with an inclinometer.
- Rounded shoulder posture
- Posterior shoulder stiffness
- Internal/external rotation range of motion (at 90° of abduction)
Medicine ball throw :
From a cocking position, players have to throw a 800g medicine ball as far as possible (3 trials). Only the best result will be retained for analysis. Volunteers have 2 minutes of rest between trials.
Upper Quarter Y Balance Test :
In a facial drop position, the purpose of this test is to bring the plastic board as far as possible in the 3 directions (supero-lateral, infero-lateral, medial). 3 trials are performed by each subject and only the best test is kept for analysis. A rest period of one minute is provided between tests to avoid fatigue.
Strength assessment (isokinetic test) :
Internal and external rotators strength (concentric 60°/s, eccentric 60°/s and concentric 240°/s) are measured with an isokinetic device (Cybex Norm) at 90° of abduction.
- Psychosocial factors assessment :
Players will have to fill in POMS questionnaire (65 questions), that give information about stress and well-being.
After that, players will be followed during all the 2019-2020 season and will have to fill in a form each month about the potential injuries they had during the previous month.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Liege, Belgium
- Belgium, Wallonia
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- age between 13 and 20
- to play volleyball at least 8 hours in a week
Exclusion Criteria:
There are no exclusion criteria
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Shoulder internal/external rotation range of motion
Time Frame: 1 month
|
Range of motion will be measured in degrees
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1 month
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Scapular dyskinesis
Time Frame: 1 month
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"yes/no" method
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1 month
|
Internal/external rotators strength
Time Frame: 1 month
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Strength of internal and external rotators will be assessed in concentric (60°/s and 240°/s) and in eccentric (60°/s) modes with an isokinetic device (Cybex Norm).
|
1 month
|
Upper Quarter Y Balance test
Time Frame: 1 month
|
The score obtained will be measured in cm and normalized by upperlimb length
|
1 month
|
Medicine ball throw
Time Frame: 1 month
|
A 800g medicine throw will have to be thrown as far as possible and the score will be measured in meters
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1 month
|
Psychosocial factors
Time Frame: up to 8 months
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Questionnaire POMS will have to be filled in by the participants each month
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up to 8 months
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Shoulder injuries
Time Frame: up to 8 months
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Participants will have to mention each month the injuries or pain they had during the previous month at shoulder location
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up to 8 months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Risk factors volleyball
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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