NCT07658404

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
78

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 10, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 10, 2026

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

June 13, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 22, 2026

Completed
Last Updated

June 22, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

June 13, 2026

Last Update Submit

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

EXPERIMENTAL

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.

Behavioral: Aerobic Exercise Program

Coordination Exercise Group

EXPERIMENTAL

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.

Behavioral: Coordination Exercise Program

Control Group

NO INTERVENTION

Participants 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.

Also known as: Aerobic Training
Aerobic Exercise Group

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.

Also known as: Coordination Training
Coordination Exercise Group

Eligibility Criteria

Age10 Years - 12 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

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)

Location

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

Locations