Risk Factors of Shoulder Injuries in Youth Volleyball Players
NCT ID: NCT04078945
Last Updated: 2022-08-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
230 participants
OBSERVATIONAL
2019-09-01
2022-07-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prevention in Volleyball Players
NCT04892121
Movement Patterns in Young Volleyball Athletes
NCT03285009
Effect of an Injury Prevention Program on the Lower Limb Stability in Young Volleyball Players
NCT04230798
Injury Risk Factors in Volleyball Players
NCT06996990
Risk Factors for Lower Extremity Overuse Injuries in Jump-landing Athletes
NCT05161273
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
At the beginning of the 2019-2020 season, they will have to take part at the following evaluations :
1. 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)
2. 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.
3. 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.
4. 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.
5. 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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* to play volleyball at least 8 hours in a week
13 Years
20 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Liege
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Camille Tooth
Physiotherapist
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Camille Tooth
Role: PRINCIPAL_INVESTIGATOR
University of Liege
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Belgium, Wallonia
Liège, , Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Risk factors volleyball
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.