- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03142243
Morphological Asymmetry in Elite Female Tennis Players (AsymFemaleTP)
Morphological Asymmetry in Elite Female Tennis Players Competing in an International Tournament in Belgium: an Observational Study
Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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-
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Brussels, Belgium, 1050
- Vrije Universiteit Brussel
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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:
- Participants will have to be professional, or elite, female tennis players.
- The players will have to participate in international tournaments in Belgium.
Exclusion Criteria:
- N/A
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Demographics
Time Frame: 01/07/2017 - 31/12/2018
|
Date of birth (in day/month/year to subsequently determine age) Gender: male or female Dominant upper extremity: right or left Dominant lower extremity: right or left Playing experience (in years) Average training hours (in hours per week) These values will be determined cross-sectionally and reported as mean and standard deviation. |
01/07/2017 - 31/12/2018
|
|
Anthropometry
Time Frame: 01/07/2017 - 31/12/2018
|
Stature (cm) Weight (kg) Body Mass Index (kg/m²) Upper extremity length (cm) Lower extremity length (cm) These values will be determined cross-sectionally and reported as mean and standard deviation. |
01/07/2017 - 31/12/2018
|
|
Body Composition
Time Frame: 01/07/2017 - 31/12/2018
|
These values will be determined cross-sectionally and reported as mean and standard deviation. In addition, all these outcome measures will be determined and reported for both the dominant and non-dominant upper and lower extremity separately. |
01/07/2017 - 31/12/2018
|
|
Morphological asymmetry
Time Frame: 01/07/2017 - 31/12/2018
|
Side-to-side difference (i.e. dominant versus non-dominant upper and lower extremity) will be calculated and expressed as a percentage (extremity symmetry index (%)) for the outcome measures described above (i.e. fat mass, muscle mass, bone mass, bone mineral content and bone mineral density). Extremity symmetry index = (measure dominant extremity or side / measure non-dominant extremity of side - 1) x 100 |
01/07/2017 - 31/12/2018
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Eva D'Hondt, PhD, Vrije Universiteit Brussel
- Study Director: Peter Clarys, PhD, Vrije Universiteit Brussel
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Other Study ID Numbers
- Asym Female Elite TP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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