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
1 other identifier
interventional
78
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 10, 2026
CompletedFirst Submitted
Initial submission to the registry
June 13, 2026
CompletedFirst Posted
Study publicly available on registry
June 22, 2026
CompletedJune 22, 2026
June 1, 2026
3 months
June 13, 2026
June 13, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Working Memory
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
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 Outcomes (2)
Motor Coordination
Baseline
Cardiorespiratory Fitness
Baseline
Study Arms (3)
Aerobic Exercise Group
EXPERIMENTALParticipants 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.
Coordination Exercise Group
EXPERIMENTALParticipants 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.
Control Group
NO INTERVENTIONParticipants continued their usual school curriculum and daily activities without receiving any additional structured exercise intervention during the study period.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Rumeli University
Istanbul, Istanbul, 34570, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
June 13, 2026
First Posted
June 22, 2026
Study Start
March 1, 2026
Primary Completion
June 10, 2026
Study Completion
June 10, 2026
Last Updated
June 22, 2026
Record last verified: 2026-06