- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07658404
Beyond Aerobic Fitness: Effects of Coordination and Aerobic Exercise on Executive Functions in School-Aged Children
Beyond Aerobic Fitness: A Randomized Controlled Trial Comparing the Effects of Coordination and Aerobic Exercise on Executive Functions in School-Aged Children
This randomized controlled trial aims to compare the effects of aerobic exercise and coordination-based exercise on executive functions in school-aged children aged 10 to 12 years. Executive functions, including working memory and selective attention, are essential cognitive skills that support learning, academic achievement, problem-solving, and daily functioning.
A total of 78 healthy children will be randomly assigned to one of three groups: an Aerobic Exercise Group, a Coordination Exercise Group, or a Control Group. Participants in the intervention groups will complete supervised exercise sessions lasting 40 minutes, three times per week, for 14 weeks. The aerobic exercise program will include activities designed to improve cardiovascular fitness, while the coordination exercise program will involve tasks requiring motor control, balance, bilateral coordination, and cognitive engagement. Participants in the control group will continue their usual school activities without additional structured exercise.
Working memory and selective attention will be assessed before and after the intervention using standardized neuropsychological tests. The findings of this study may improve understanding of how different types of physical activity influence cognitive development in children and may help educators and health professionals design more effective school-based physical activity programs that support both physical and cognitive health.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Istanbul
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Istanbul, Istanbul, Turkey (Türkiye), 34570
- Istanbul Rumeli University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children aged between 10 and 12 years.
- Typically developing children without diagnosed neurological, developmental, or physical disorders.
- Written informed consent obtained from parents or legal guardians.
- Child assent provided before participation.
Exclusion Criteria:
- Diagnosis of attention-deficit/hyperactivity disorder (ADHD).
- Presence of learning disabilities.
- Neurological, developmental, or chronic medical conditions limiting participation in physical activity.
- Attendance of less than 80% of the intervention sessions.
- Occurrence of health problems during the study period that prevented continued participation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Aerobic Exercise Group
Participants completed a supervised aerobic exercise program for 14 weeks, consisting of 40-minute sessions conducted three times per week.
The program included high-intensity interval activities, sprint running, and game-based aerobic exercises designed to improve cardiorespiratory fitness.
|
Participants completed a supervised aerobic exercise program for 14 weeks.
Exercise sessions were conducted three times per week and lasted 40 minutes each.
The intervention included high-intensity interval activities, sprint running, and game-based aerobic tasks designed to improve cardiorespiratory fitness.
Exercise intensity was monitored using heart rate monitors, and participants maintained an intensity corresponding to 65% to 85% of their age-predicted maximum heart rate.
Other Names:
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|
Experimental: Coordination Exercise Group
Participants completed a supervised coordination-based exercise program for 14 weeks, consisting of 40-minute sessions conducted three times per week.
Activities included jump-rope combinations, dynamic balance exercises, bilateral coordination tasks, and multidirectional movement tasks requiring cognitive engagement.
|
Participants completed a supervised coordination-based exercise program for 14 weeks.
Exercise sessions were conducted three times per week and lasted 40 minutes each.
The intervention included jump-rope combinations, dynamic balance exercises, bilateral coordination activities, and multidirectional movement tasks requiring cognitive engagement.
Exercise intensity was standardized using ratings of perceived exertion, targeting Borg scale scores between 13 and 16.
Other Names:
|
|
No Intervention: Control Group
Participants continued their usual school curriculum and daily activities without receiving any additional structured exercise intervention during the study period.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Working Memory
Time Frame: Baseline and Week 14
|
Working memory performance will be assessed using the Visual-Auditory Digit Span Test.
The test evaluates the ability to temporarily store, manipulate, and recall information through auditory and visual modalities.
Higher scores indicate better working memory performance.
|
Baseline and Week 14
|
|
Selective Attention
Time Frame: Baseline and Week 14
|
Selective attention will be assessed using the d2 Test of Attention.
Outcome measures include concentration performance, processing speed, and error rates.
Higher concentration scores indicate better selective attention performance.
|
Baseline and Week 14
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Motor Coordination
Time Frame: Baseline
|
Motor coordination will be evaluated using the Körperkoordinationstest für Kinder (KTK) test battery.
The assessment includes balance, jumping, and movement coordination tasks, with scores converted into an overall Motor Quotient.
|
Baseline
|
|
Cardiorespiratory Fitness
Time Frame: Baseline
|
Cardiorespiratory fitness will be assessed using the 20-meter shuttle run test.
Maximal oxygen uptake (VO₂max) will be estimated from test performance.
|
Baseline
|
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
- IRU-2026-02-08
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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