The Relationship Between Body Composition and Physical Fitness in Young Male Basketball Players

March 19, 2024 updated by: Gökhan Can TÖRPÜ, Bezmialem Vakif University

In this study, it is aimed to investigate the relationship between body composition, aerobic capacity, trunk muscle endurance and muscle strength in young male basketball players.

The study will take place at a local basketball academy. Young male athletes between the ages of 10-24 and enrolled in a basketball academy will be included in the study. Participants who have been involved in basketball for less than a year, and those who have injuries that prevent participation in the study will be excluded.

Study Overview

Status

Completed

Detailed Description

Individual development differences in young people can have an impact on physical fitness components such as aerobic capacity, trunk muscle endurance and muscle strength required for basketball. At the same time, differences in these components can have effects on each other.

There is a complex relationship between anthropometric changes during growth and physical fitness because many differences can occur during the physiological development of players. In this context, differences in growth rate and development in young basketball players are complex factors that affect game performance and player success. Characteristics such as body height, body weight, skeletal muscle ratio and body fat are among the basic anthropometric components of a basketball player, and these components are considered to be important indicators of a player's game performance.

Study Type

Observational

Enrollment (Actual)

29

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

    • Eyüp
      • Istanbul, Eyüp, Turkey, 34060
        • Eyüp Basket Akademi

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Young male basketball players enrolled in a local basketball academy

Description

Inclusion Criteria:

  • Male gender
  • Being between the ages of 10-24

Exclusion Criteria:

  • Athlete's own or family refusal to participate in the study
  • Interested in basketball for less than a year
  • Having an injury that would prevent participation in the study

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Young Male Basketball Players
Male athletes between the ages of 10-24 who are involved in a local basketball academy and have been involved in basketball for more than a year
The OMRON BF511 Body Composition Monitor is a digital scale and participants' body compositions will be evaluated with this device. The aerobic capacities of the participants will be evaluated with the Multi-Stage 20 m Shuttle Run Test and the maximum oxygen consumption levels will be calculated with the help of the formula with the data obtained from this test. The trunk extensor muscle endurance of the participants will be evaluated with the Biering-Sorensen Test and the trunk flexor endurance will be evaluated with the Kraus-Weber Test. Participants' M. Quadriceps, M. Hamstring, M. Biceps Brachii and M. Triceps Brachii muscle strengths will be evaluated with MicroFET® 2 hand dynamometer.
Other Names:
  • Multi-Stage 20 m Shuttle Run Test
  • Biering-Sorensen Test and Kraus-Weber Test
  • MicroFET® 2 hand dynamometer

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body Weight
Time Frame: One Month
Participants' body weights will be evaluated with the OMRON BF511 Body Composition Monitor and recorded in kilograms (kg).
One Month
Body Height
Time Frame: One Month
The body lengths of the participants will be evaluated with a tape measure and recorded in meters (m).
One Month
Body Mass Index
Time Frame: One Month
The body mass index of the participants will be calculated and recorded with the formula kg/m^2.
One Month
Body Fat
Time Frame: One Month
Participants' body fat will be evaluated with the OMRON BF511 Body Composition Monitor and recorded in percent (%).
One Month
Skeletal Muscle Mass
Time Frame: One Month
Participants' skeletal muscle mass will be evaluated with the OMRON BF511 Body Composition Monitor and recorded in percent (%).
One Month
Visceral Fat
Time Frame: One Month
Participants' visceral fat will be evaluated with the OMRON BF511 Body Composition Monitor and recorded in levels.
One Month
Resting Metabolic Rate
Time Frame: One Month
Participants' visceral fat will be evaluated with the OMRON BF511 Body Composition Monitor and recorded in kilocalories (kcal).
One Month
Aerobic Capacity
Time Frame: One Month
Maximum oxygen consumption (VO2max)
One Month
Trunk Muscle Endurance
Time Frame: One Month
Trunk extensor muscle endurance will be evaluated with Biering-Sorensen Test and trunk flexor muscle endurance will be evaluated with Kraus-Weber Test. The maximum time the participants can continue the test will be recorded in seconds.
One Month
Muscle Strength
Time Frame: One Month
M. Quadriceps, M. Hamstring, M. Biceps Brachii and M. Triceps Brachii muscles will be evaluated in Newtons (N) with MicroFET® 2 hand dynamometer.
One Month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Semiramis Özyılmaz, PhD, Bezmialem Vakif University
  • Principal Investigator: Gökhan C Törpü, BPT, Bezmialem Vakif University
  • Study Chair: Selva Otsay, BPT, Bezmialem Vakif University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

July 15, 2023

Primary Completion (Actual)

August 2, 2023

Study Completion (Actual)

August 2, 2023

Study Registration Dates

First Submitted

June 15, 2023

First Submitted That Met QC Criteria

June 23, 2023

First Posted (Actual)

July 3, 2023

Study Record Updates

Last Update Posted (Actual)

March 20, 2024

Last Update Submitted That Met QC Criteria

March 19, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • BezmialemVU-KFR-GCT-01

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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