- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05587907
Reaction Time, Cognitive Function and Physical Fitness of Children and Adolescent Soccer Players
The Effect of an Exercise Program With Visual Stimuli on Reaction Time, Cognitive Function and Physical Fitness of Children and Adolescent Soccer Players
Study Overview
Detailed Description
38 male soccer players aged 10-15 participate in the research voluntarily. A wireless reflex measurement system (FITLIGHT Trainer) is used to measure the response time, a cognitive function test (Cognitive Function Scanner Mobile) is used to assess cognitive function and an interactive virtual reality application (VR game) is used to estimate the visual field. Physical fitness is assessed using ALPHA-Fitness and the Eurofit test batteries. The screening takes place in the soccer field with portable devices. After the initial check, the participants were randomly divided into two equal groups using the program http://www.randomizer.org/.
18 soccer players follow a 6-month exercise program with visual stimuli, 5 times a week and lasting 15 minutes each time, which precedes their regular soccer training program. The special training program includes training using illuminated units / disks. Each unit is activated alternately, and it is deactivated when the trainee passes in front of it or touches it with any part of his body as well as with another object / sports accessory. The remaining players continue their regular soccer training program. After the end of the 6 months, the initial measurements will be repeated in both groups.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Thessaloniki, Greece, 57001
- Laboratory of Sport Medicine, Department of Physical Education and Sports Sciences Aristotle University of Thessaloniki
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria: male sex, age 10-15 years, soccer experience ≥ 1year
Exclusion Criteria: None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Group 1
18 soccer players follow a 6-month exercise program with visual stimuli, 5 times a week and lasting 15 minutes each time, which precedes their regular soccer training program.
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Evaluation of the reaction time before and after special training program using visual stimuli.
Other Names:
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NO_INTERVENTION: Group 2
20 soccer players follow a regular soccer training program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reaction time (sec)
Time Frame: 6 months
|
VR game, FITLIGHT Trainer
|
6 months
|
Cognitive function (sec)
Time Frame: 6 months
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Cognitive Function Scanner Mobile
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Physical fitness
Time Frame: 6 months
|
RFD (kg/sec), Hand grip test (kg), Sit & reach flexibility (cm), Repeated Sprint (sec)
|
6 months
|
Collaborators and Investigators
Investigators
- Study Chair: EVANGELIA KOUIDI, PhD, Department of Physical Education and Sports Sciences Aristotle University of Thessaloniki, Greece
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
Keywords
Other Study ID Numbers
- 68/2021
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
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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