- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04245904
Comparison of Respiratory Functions and Physical Fitness Parameters of Professional Basketball Players With Sedentary Controls
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Ankara, Turkey, 06230
- Hacettepe University
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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:
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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
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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proffesional basketball player
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sedentary control
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
respiratory muscle strenght
Time Frame: day 1
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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.
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day 1
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respiratory muscle endurance
Time Frame: day 1
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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
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Total body weight
Time Frame: day 1
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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
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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.
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day 1
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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
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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.
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day 1
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VO2max
Time Frame: day 2
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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
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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).
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day 2
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20 m speed test
Time Frame: day 1
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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.
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day 1
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reaction time
Time Frame: day 2
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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 .
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day 2
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- GO 19/52
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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