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Beyond Aerobic Fitness: Effects of Coordination and Aerobic Exercise on Executive Functions in School-Aged Children

2026年6月13日 更新者:Görkem Açar、Istanbul Gelisim University

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.

研究概览

研究类型

介入性

注册 (实际的)

78

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Istanbul
      • Istanbul、Istanbul、土耳其(türkiye)、34570
        • Istanbul Rumeli University

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子

接受健康志愿者

是的

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的: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.
其他名称:
  • 有氧训练
实验性的: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.
其他名称:
  • Coordination Training
无干预:Control Group
Participants continued their usual school curriculum and daily activities without receiving any additional structured exercise intervention during the study period.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Working Memory
大体时间: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
大体时间: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

次要结果测量

结果测量
措施说明
大体时间
Motor Coordination
大体时间: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
大体时间:Baseline
Cardiorespiratory fitness will be assessed using the 20-meter shuttle run test. Maximal oxygen uptake (VO₂max) will be estimated from test performance.
Baseline

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年3月1日

初级完成 (实际的)

2026年6月10日

研究完成 (实际的)

2026年6月10日

研究注册日期

首次提交

2026年6月13日

首先提交符合 QC 标准的

2026年6月13日

首次发布 (实际的)

2026年6月22日

研究记录更新

最后更新发布 (实际的)

2026年6月22日

上次提交的符合 QC 标准的更新

2026年6月13日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • IRU-2026-02-08

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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