- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05789472
The Relationship Between Reaction Time and Executive Functions in Female Athletes
The Relationship Between Reaction Time and Executive Functions in Amateur Female Athletes Playing Team Sports
Study Overview
Detailed Description
Executive functions are often described as 'higher cognitive processes' that govern other basic cognitive functions. Executive functions include higher-order cognitive abilities such as planning, decision making, problem solving, strategizing, working memory, inhibition, cognitive flexibility, abstraction, and reasoning. It enables individuals to organize their thoughts and actions during goal-directed behavior, to think, to produce ideas, to respond and to control in the face of unexpected situations.
Response time is the time elapsed after the stimulus reaches the body until the first response to these stimuli. It is the time between the first reaction that occurs after the appearance of a sensory, visual or tactile stimulus. Athletes must respond quickly to a ball, the movement of another athlete, or incoming signals to compete successfully and avoid injury. The reaction time depends on the neurophysiological processes in the brain.
In our study, which was planned to evaluate the relationship between reaction time and executive functions in 66 amateur female athletes between the ages of 18-25, who are university football, basketball and volleyball team athletes; The age, body mass index (BMI), sports branch, duration of interest in sports will be recorded in the demographic information form. Hand-eye and foot-eye reaction time of the athletes will be evaluated by BlazePod Reaction Time Determination Test and executive functions will be evaluated with Forward-Backward Number Range test, Stroop test and Tracking A-B test.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Atatürk Street
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Istanbul, Atatürk Street, Turkey, 34810
- Gülay Aras Bayram
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- At least 5 years of sports
- Being an athlete on university sports teams
Exclusion Criteria:
- Athletes with health problems (eg cancer, arthritis, heart disease, lung disease, neurological or psychological illness)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Football Group
Assessment
|
Executive functions and reaction times of all participants will be measured.
|
|
Experimental: Basketball Group
Assessment
|
Executive functions and reaction times of all participants will be measured.
|
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Experimental: Volleyball Group
Assessment
|
Executive functions and reaction times of all participants will be measured.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
BlazePod Reaction Time Determination Test
Time Frame: 1 day
|
The BlazePod test, which includes "pods" equipped with touch sensors and LED lights, will be used to evaluate the reaction time. In the evaluation, the number of 15 seconds of touch (number), the reaction time (ms) for the visual response of 15 seconds of touch, and the average reaction time will be analyzed. |
1 day
|
|
Forward-Backward Number Range Test
Time Frame: 1 day
|
The test consists of two parts as forward and backward range.
In the forward number range, the numbers are read at one-second intervals and the patient is asked to repeat the numbers read randomly in the same order.
In the back number range, it is requested to repeat the numbers read from the end to the beginning.
As you succeed, it continues by increasing one step.
If the patient fails twice in a row for both sections, the test is discontinued.
Generally, the difference between the forward and backward number range is expected to be two digits.
The highest score that can be obtained for the forward range is 8 points, and 7 for the backward range, for a total of 15 points.
|
1 day
|
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Stroop Test
Time Frame: 1 day
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The test consisting of 6 lines of random blue, green, red colors and including three basic tasks; In the first task, the individual is asked to name the colors in the box.
In case of successful completion, the second task, the words written with the same colors, is asked to be read and the time is kept.
In the third task, the words are asked to inhibit reading and to say in which color they are written.
The time to finish the test, the number of errors, and the number of spontaneous corrections are noted.
|
1 day
|
|
Tracking Test
Time Frame: 1 day
|
The trail riding test consists of two parts, A and B. In part A, the participants are asked to combine the circles with the numbers in the correct order and following each other (1-2-3-4-5...).
In section B, there are letters and numbers placed in circles.
Participants are asked to combine letters and numbers in the correct sequence (1-A-2-B-3-C-4-D...).
The times of both sections are recorded.
The trailing test requires visuospatial processing and motor skills.
Particularly, part B is widely used in the measurement of complex attention, planning, set-changing, and reaction inhibition among executive functions.
|
1 day
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gülay Aras Bayram, PhD, Medipol University
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
- 119 (hhh)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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