Comparison of Respiratory Functions and Physical Fitness Parameters of Professional Basketball Players With Sedentary Controls

January 26, 2020 updated by: Hilal GÜNGÖR, Hacettepe University
The aim of the study was to compare the professional basketball players and sedentary controls in terms of respiratory function and physical fitness parameters and to investigate the relationship between respiratory function and physical fitness parameters in basketball players.

Study Overview

Status

Completed

Detailed Description

Basketball is one of the most common team sports in the world, where aerobic and anaerobic power is used together and taking into account the rising number of participants in non-professional leagues, it is especially popular among female athletes from various countries . Basketball players' muscular strength and endurance, power, speed, agility and physical properties such as reaction time are the main factors underlying the performance. In addition to this, respiratory functions are important as well as physical properties in basketball. Because during the maximal exercise, the blood flow to the inspiratory and expiratory muscles accounts for 15% of the total oxygen cost of the exercise. Assessment of the motor skills and physical characteristics of basketball players is very important for the positioning of the player, performance analysis and monitoring the effectiveness of the training. There are many studies examining the physical fitness characteristics of basketball players.However, no study evaluating respiratory muscle strength and endurance in female basketball players was found in the literature.therefore, this study was planned.

Study Type

Observational

Enrollment (Actual)

42

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

      • Ankara, Turkey, 06230
        • Hacettepe University

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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Probability Sample

Study Population

A team playing professional basketball in Turkey in Super League Basketball Women Study (mean age, 24.24 ± 4.96 years), basketball and sedentary individuals of the same age and sex were included on a voluntary basis. Permits were obtained from the necessary institutions before the studies to be made to the athletes. A total of 42 people from 21 people were included in the study according to 5% Type1 error, two-way hypothesis test design and sample size calculation with at least 80% working power. Before the measurement protocols, the participants were informed about the study and informed consent form was obtained.

Description

Inclusion Criteria:

-

Inclusion criteria of basketball players:

  • Female athletes with at least 3 years of professional basketball experience
  • Volunteer to participate in the study
  • 18-35 years
  • Participating in training sessions regularly
  • Non-smoking
  • Do not use any supplements or medicines that affect physical performance

The inclusion criteria for healthy sedentaries were:

  • 18-35 years old women
  • Volunteering
  • Have never done sports
  • No smoking

Exclusion Criteria:

  • • Doing any sport except basketball

    • Chronic respiratory or cardiovascular disease
    • Have had respiratory tract infection at least 4 weeks before the test (potential effect on respiratory muscle strength)
    • Have had an orthopedic injury in the last 3 months
    • Abandoned tests for any reason
    • Leaving the team or transferring to another team

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

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
proffesional basketball player
sedentary control

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
respiratory muscle strenght
Time Frame: day 1
Respiratory muscle strength was assessed by an electronic mouth pressure measuring device (Micro Medical, Kent, UK) measuring MIP and MEP according to the American Thoracic Society (ATS) and European Respiratory Society (ERS) criteria . At least three measurements were taken. Between the measurements were given 1 minute rest. MIP was measured during deep inspiration after expiration up to the residual volume. Nasal respiration was prevented with the help of clips by asking the participants to evacuate all air from the nose and they were asked to breathe with maximum inspiratory effort. MEP was measured during deep expiration up to total lung capacity. After nasal breathing was prevented, the person was asked to exhale with maximum effort . Values were calculated according to age and gender variables using Black and Haytt's reference thresholds and recorded as a percentage of expected values.
day 1
respiratory muscle endurance
Time Frame: day 1
Respiratory muscle endurance was measured by the incremental load testing with Power Breathe (HaB International Ltd. Southam, UK). The test was completed when it was not tolerated in case of shortness of breath and fatigue. The duration of the person's performance in different workloads was recorded. A workload level of less than one minute is considered invalid and a lower level is recorded. The results are obtained by multiplying the maximum workload in more than one minute and time values in seconds.
day 1
Total body weight
Time Frame: day 1
Total body weight (kg) of the participants were measured using a digital scale (BC-418 MA, Tanita®, Japan) sensitive to fasting up to 0.1 kg on an empty stomach.
day 1
Body fat percentage
Time Frame: day 1
Body fat percentage (%), of the participants were measured using a digital scale (BC-418 MA, Tanita®, Japan) sensitive to fasting up to 0.1 kg on an empty stomach.
day 1
fat free mass (FFM)
Time Frame: day 1
(FFM) (kg) of the participants were measured using a digital scale (BC-418 MA, Tanita®, Japan) sensitive to fasting up to 0.1 kg on an empty stomach.
day 1
Body mass index
Time Frame: day 1
The body mass index (BMI) of the participants was calculated according to the body weight / height2 (kg / m2) formula according to WHO criteria.
day 1
VO2max
Time Frame: day 2

20 meters shuttle running test: It is a multistage test, commonly used to estimate VO2max, with the first stage being warming up. In this test, individuals performed 2X20 meter shuttle runs between the start and finish lines at a starting speed of 8.5 km / h and incremental speeds of 0.5 km / h per minute. The running speed was determined by automatic warning sounds from the CD player. The test consists of 21 levels and each level lasts 1 minute. The test was terminated when the participant ran out of power or delayed reaching the finish line twice. According to the score form of the test, the level of the participants' running was recorded and the "distance koş considered as the basis for the performance. VO2max total calculated distance was calculated by substituting in the formula (66.88).

VO2max = 20.6 + Final stage completed x3 (88)

day 2
T-Drill test
Time Frame: day 2
T-Drill Test for Agility The T-Drill test was performed using the protocol specified by Semenick (89). The three funnels were placed in the same direction with 5 yards (5 yards = 4.57 m) apart. The other funnel was placed at a distance of 10 yards from the center of the funnels (in the form of the letter T). It includes 5 steps to the left (5 yards = 4.57 m), 10 steps to the right (10 yards = 9.14 m), 5 steps to the left, 10 steps backwards. At the starting point (0 meters), the person finished the test with one of the knees in front and one in the back, then stepping forward, left, right, and backward at maximum speed. Three replicates were taken for each participant. 3 minutes of rest was given between each trial. The measurement results were recorded in seconds. The best score was used for statistical analysis after three trials (90).
day 2
20 m speed test
Time Frame: day 1
The 20 meter (m) speed test was used for the speed values of the participants. Stopwatch was used for 20 m speed test. For the test, two cones at 20 m intervals and three cones in the form of a cone at 25 m were placed in the same direction. Participants were asked to continue up to 25 m so that they did not slow down without completing the test. The starting position of the participant was to place one of his feet not to exceed the exit funnel. The time until the person crossed the cone at 20 m was recorded after the person exited with the signal given while the participant was ready in the starting position. The test was taken 3 times at 2 min intervals. The values were saved in seconds. The shortest time was evaluated.
day 1
reaction time
Time Frame: day 2
The reaction time was measured by Fitlight Trainer ™ (Fitlight Traniner Corperation, Thensvej, Risskov, Denmark). Hand reaction speed test: With the Fitlight TrainerTM, six LED lights placed at certain points on the wall were lit randomly and the person was asked to turn them off as fast as possible. In the protocol, the LEDs were placed according to the physical structure of the person and the number of seconds in which the 29 LEDs were extinguished were recorded in seconds .
day 2

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 15, 2019

Primary Completion (Actual)

April 15, 2019

Study Completion (Actual)

June 8, 2019

Study Registration Dates

First Submitted

December 28, 2019

First Submitted That Met QC Criteria

January 26, 2020

First Posted (Actual)

January 29, 2020

Study Record Updates

Last Update Posted (Actual)

January 29, 2020

Last Update Submitted That Met QC Criteria

January 26, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • GO 19/52

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

product manufactured in and exported from the U.S.

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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