The Effect of Cognitive Performance on Physical Performance in Adolescent Basketball Players
Study Overview
Status
Status
Conditions
Conditions
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Naime Uluğ, PhD.
- Phone Number: +905365434409
- Email: naime.ulug@atilim.edu.tr
Study Contact Backup
- Name: Seyde Büşra Kodak, MSc.
- Phone Number: +905511607016
- Email: seyde.kodak@ahievran.edu.tr
Study Locations
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Ankara, Turkey
- Atılım University
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Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Male basketball players between the ages of 14-18,
- To be a licensed athlete for at least 5 years,
- Being active in sports and training for the last 1 year,
- Weekly training intensity is at least 5 hours per week
Exclusion Criteria:
- Having a history of visual, mental or systemic disease,
- Having a history of major injury in the medical history,
- Any complaints of acute or chronic pain/injury
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reactive Agility
Time Frame: 25 June 2023
|
For the test, the athletes were positioned in the middle of the distance of 16 feet (4.88 meters), 2 meters in front of the warning screen.
A and B funnels were introduced to the athlete.
When the test started, the warning screen started counting down from 3; at the end of the count, it gave one of the warnings A or B as a random warning.
As soon as the athlete saw the warning, he started the test in the direction of the warning that appeared on the screen.
The time elapsed between the appearance of the A or B warning on the screen and the athlete's perception and response (knee flexion) was recorded as "reaction time" by watching the Movavi Video Editor Plus 2022 program.
After starting the test, the athlete ran and touched the first funnel he turned to, then came back and touched the other funnel. .
He turned back to the funnel he touched first and passed through the photocells, completing the test.
The time from start to finish was recorded as "reactive agility score".
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25 June 2023
|
|
Lower Extremity Strength
Time Frame: 25 June 2023
|
Microgate Witty Brand vertical jump mat was used to evaluate the vertical jump height.
The device consists of 2 parts, a matte and a tablet.
For the test, the athlete was asked to jump on the mat as described.
When the athlete performed the vertical jump, the jump height was recorded by reading from the tablet screen.
Before the test, the athletes were given 2 repetitive vertical jumps for trial purposes.
|
25 June 2023
|
|
Agility
Time Frame: 25 June 2023
|
Agility T Test was used to evaluate Agility.
The T-Test was performed using a standardized version from the previous literature [65].
A 10 × 10 meter course was created for the test.
The funnels defining the boundaries of the track were numbered.
Athletes were asked to return to the cone alignments according to the order specified for the test.
|
25 June 2023
|
|
Running Speed
Time Frame: 25 June 2023
|
The 20-meter sprint test was used to evaluate the running speed.
A 20-meter track was prepared for the test.
Athletes were asked to run the 20-meter distance as fast as possible.
The fastest time to complete the track was recorded as a score in seconds.
Microgate Witty brand photocells were placed at the start and end points to measure the time [66, 67].
The device consists of 3 parts, 2 photocell doors and tablet Photocell doors were positioned on both sides of the start and finish lines.
For the test, the athlete started the photocell counter as soon as the athlete crossed the starting line.
The finish photocell stopped the counter as soon as the athlete crossed the finish line.
|
25 June 2023
|
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Balance
Time Frame: 25 June 2023
|
Y-Shaped Balance Test was used to evaluate upper extremity balance.
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25 June 2023
|
|
Right/Left Separation
Time Frame: 25 June 2023
|
Android-based Noi Recognise App application was used for the right-left separation of the athletes.
Before the test, the practice was shown to the athletes and a trial test was performed.
The test was performed with a mobile device while the athletes were in a sitting position.
20 different images of hands photographed from different angles, used as standard for the test, were shown 5 seconds apart.
The athlete was asked to mark which side extremity the picture he saw belonged to as quickly and accurately as possible on the screen of the application.
Recognition rates and response speed obtained as a result of the test were recorded as scores on the application.
|
25 June 2023
|
|
Stroop Test
Time Frame: 25 June 2023
|
The Stroop test is widely used to evaluate cognitive functions such as selective attention and resistance to interference.
There are different variations of the Stroop test.
In our study, we used the Stroop Test Anchor Form, the validity and reliability of which was made by Savaş et al.
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25 June 2023
|
|
Two-Point Discrimination
Time Frame: 25 June 2023
|
Baseline 2-point discrimination instrument was used for the two-point discrimination test.
The discrimination tool was set to 5 millimeters.
The tips of the instrument were touched to the most swollen area of the hypothenar region of the dominant hand, parallel to the long axis of the hand, and they were asked to say how many points they felt.
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25 June 2023
|
|
Pain Threshold Level
Time Frame: 25 June 2023
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Jtech Commander (JTech Medical Industries, ZEVEX Company) brand algometer device was used to evaluate the pain threshold.
The most swollen point of the thenar region of the dominant hand was used to assess the pain threshold.
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25 June 2023
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- E-59394181-604.01.02-32301
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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