- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04495595
Influence of the Biological Maturation on the Antrhopometric Variables and Sport Performance in Volleyball Players
July 19, 2021 updated by: Mario Albaladejo-Saura, Universidad Católica San Antonio de Murcia
The project consists of a cross-sectional study in which anthropometric variables, general and specific performance variables of volleyball will be measured, and the biological maturity stage will be calculated.
The main objective is to establish a relationship between the biological maturation state, the anthropometric characteristics and the performance in physical fitness tests in volleyball players between 12 and 15 years of age.
To do this, there will be all the clubs in the Region of Murcia that have federated teams in these categories.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
213
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Murcia, Spain
- Universidad Católica San Antonio
-
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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
12 years to 15 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The sample objetive of the present study are all the volleyball players of Región of Murcia, Spain, that meet the inclusion criteria and voluntarily decide to take part in the study.
Description
Inclusion Criteria:
- To play volleyball in a regular basis
- To have between 12 and 15 years
- To participate in volleiball competitions with the team
Exclusion Criteria:
- To be injured in the moment of the measurement session
- To have skipped most of the training sessions the last month
- To have less than a year of experience playing volleyball
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Volleyball performance
Time Frame: through study completion, an average of 1 year
|
Qualitative assessement of the individual sport performance, taking on account the team position on the league and the role of the player in the team.
The instrument used to assess this variable will be a questionnaire and the result will be expressed in points (1 to 5 points).
|
through study completion, an average of 1 year
|
Biological maturation
Time Frame: through study completion, an average of 1 year
|
Calculated with anthropometric variables.
The result obtained indicates the time left to the growth peak or the time that has passed from the growth peak
|
through study completion, an average of 1 year
|
Muscle mass
Time Frame: through study completion, an average of 1 year
|
Muscle mass will be assessed with the corresponding formulas.
The result will be expressed in kilograms
|
through study completion, an average of 1 year
|
Fat mass
Time Frame: through study completion, an average of 1 year
|
Fat mass will be assessed with the corresponding formulas.
The result will be expressed in kilograms
|
through study completion, an average of 1 year
|
Bone mass
Time Frame: through study completion, an average of 1 year
|
Bone mass will be assessed with the corresponding formulas.
The result will be expressed in kilograms.
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
January 13, 2020
Primary Completion (Actual)
March 4, 2021
Study Completion (Actual)
March 4, 2021
Study Registration Dates
First Submitted
July 23, 2020
First Submitted That Met QC Criteria
July 28, 2020
First Posted (Actual)
August 3, 2020
Study Record Updates
Last Update Posted (Actual)
July 20, 2021
Last Update Submitted That Met QC Criteria
July 19, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CE061921
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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