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Effects of a 6-Month Gymnastics Program on Somatotype and Motor Performance in Children Across Age Groups (Motor Progress)

2026年5月26日 更新者:Ahmet KURTOĞLU、Bandırma Onyedi Eylül University
The study adopted a controlled 6-month study design to compare the gymnastics group (n= 56) with the inactive control group (n=88). Anthropometric profiling, somatotype assessment, and motor performance tests were conducted pre- and post-intervention

研究概览

详细说明

The study design for the present investigation was prospective, controlled, and observational with a duration of 6 months. The repeated measures design approach has been used to assess the neuromuscular and morphological adaptations (Pre-test vs. Post-test) for the gymnastics and inactive groups. The intervention and observation period for the study was 2 days x 24 weeks.

To ensure high internal validity and to minimize the effects of circadian rhythm changes, all pre- and post-test assessments were conducted during the morning hours, between 09:00 and 11:30 AM, under similar environmental conditions (temperature and humidity). Prior to the pre-test, standardized pre-test procedures were clearly explained to the participants and their parents. Children were instructed to adhere to their routine sleeping habits (minimum 8 hours of sleep) and abstain from any strenuous physical activity and sports for at least 24 hours prior to the pre- and post-test assessments.

With regard to the standardized nutritional conditions, the participants were instructed to adhere to their routine diet but abstain from heavy meals for at least 2 hours prior to the pre- and post-test assessments. Participants were allowed to drink water ad libitum up to 30 minutes prior to the assessments.

On the assessment days, a logical and non-fatiguing sequence of the pre- and post-test assessments was strictly followed. Non-invasive anthropometric assessments such as stature, body mass, skinfolds, girths, and breadths were conducted for all the participants, while they were in a rested and non-sweated condition. After the anthropometric assessments, the participants were administered a standardized 10-minute dynamic warm-up procedure by a certified strength and conditioning specialist. Subsequently, the motor performance tests were conducted. To prevent the participants from fatigue, the physical tests were conducted from the least to the most fatiguing, from flexibility to muscular endurance and sprint capacity, with strict adherence to the intervening time of 3-5 minutes between the assessments

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研究类型

介入性

注册 (实际的)

144

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

      • Astana、哈萨克斯坦
        • Kazakh National University of Sports

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:

  • For Experimental Group: Active and continuous participation in a gymnastics program during the entire 6-month period.
  • Inactive control group : comprised participants who did not practice any form of sports, athletics, and physical training outside their usual physical education classes at school.

Exclusion Criteria:

  • the presence of any chronic metabolic, cardiovascular, and endocrine disorders;
  • a history of severe musculoskeletal injuries and orthopedic surgeries within the past year;
  • the use of medications known to have a significant impact on body composition and physical performance; and
  • an attendance rate of less than 85% for the gymnastics sessions (only for the intervention group).

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:治疗
  • 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:实验组
Gymnastic Training for six month
无干预:控制组

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
Circumferences (Girths) Measurements
大体时间:6 month
Girth measurements were taken to the nearest 0.1 cm using a flexible, non-stretchable anthropometric tape measure (Lufkin W606PM, Apex Tool Group). The measured girths included the head, neck, shoulder, chest, waist, hip, relaxed arm, forearm, thigh, maximum calf, and ankle circumferences. Care was taken to ensure the tape measure was at a right angle to the long axis of the body segment and did not compress the subcutaneous tissue.
6 month
Skinfold Thickness Measurements
大体时间:6 month
Skinfold thicknesses were measured to the nearest 0.1 mm using a Harpenden skinfold caliper (Baty International, West Sussex, UK). Measurements were taken in duplicate at nine standardized sites: triceps, subscapular, biceps, chest, axillary, abdominal, suprailiac, anterior thigh, and medial calf. If the difference between the first two measurements exceeded 5%, a third measurement was taken, and the median value was recorded for analysis. Furthermore, to obtain a comprehensive and robust quantification of total subcutaneous adiposity, the sum of all nine measured skinfolds (Σ9SF) was calculated. In pediatric kinanthropometry, the absolute sum of multiple skinfold sites is widely recognized as a highly reliable proxy for total body fatness, as it circumvents the inherent biological maturation errors and prediction biases associated with population-specific body density and body fat percentage equations.
6 month
Waist-to-Height Ratio
大体时间:Six Month
Calculated by dividing waist circumference (cm) by standing height (cm). This ratio serves as a highly validated, age-independent proxy for central adiposity and health risk in pediatric populations.
Six Month
Segment Lengths and Bone Breadths Measurements
大体时间:Six Month
Segment lengths (arm span, total arm, forearm, total leg, thigh, tibia, and foot lengths) were measured using a segmometer and anthropometric tape to the nearest 0.1 cm. Skeletal breadths were measured to the nearest 0.1 cm using a sliding spreading caliper. The breadth measurements included the shoulder, biacromial, biiliac, bitrochanteric, knee (biepicondylar femur), elbow (biepicondylar humerus), and wrist.
Six Month
Body Fat (BF) and Fat-Free Mass
大体时间:six month
Relative body fat percentage (BF%) was estimated using the pediatric-specific skinfold equations developed by Slaughter et al. Specifically, this calculation utilized the sum of the triceps and subscapular skinfold thicknesses, adjusted for biological sex and maturation, which is considered the gold standard for clinical field assessments in youth. Subsequently, total body fat mass was determined, and absolute Fat-Free Mass (FFM in kg) was calculated by subtracting this estimated fat mass from the total body mass.
six month
Skeletal Muscle Mass
大体时间:six month
Total skeletal muscle mass (kg) was estimated by employing validated anthropometric prediction models for children and adolescents, which account for standing height as well as corrected limb girths (i.e., thigh, calf, and arm circumferences that have been corrected for their respective overlying subcutaneous adipose tissue thicknesses).
six month
Arm Muscle Area
大体时间:six month
AMA was calculated to estimate regional upper-body muscularity and protein reserves. AMA (cm²) was derived from relaxed arm girth (cm) and triceps skinfold thickness (cm) using the standard anthropometric equation
six month
Somatotype
大体时间:six month

The anthropometric somatotype components, namely endomorphy, mesomorphy, and ectomorphy, were calculated according to the Heath-Carter method [17, 24].

Endomorphy was estimated based on the height-adjusted sum of three skinfold thicknesses: triceps, subscapular, and suprailiac.

six month
Motor Performance Tests
大体时间:six month

Flexibility (Sit and Reach Test):

Lower-Body Explosive Power:

Muscular Endurance:

Speed (20-m Sprint):

six month
Body Composition
大体时间:6 months

Endomorphy was estimated based on the height-adjusted sum of three skinfold thicknesses: triceps, subscapular, and suprailiac.

Mesomorphy was determined using humerus (elbow) breadth, femur (knee) breadth, height, and corrected limb girths. Corrected arm girth (CAG) and corrected calf girth (CCG) were adjusted for the corresponding skinfold thicknesses.

Ectomorphy was derived from the Height-Weight Ratio (HWR), which was calculated as height divided by the cube root of body mass.

6 months
Weight
大体时间:6 Month
Participants were assessed barefoot and wearing minimal clothing. Participants' body weight was measured using a Seca (Seca GmbH, Hamburg, Germany) scale with an accuracy of 0.1 kg.
6 Month
Height
大体时间:6 month
Participants' height was measured using a Seca (Seca GmbH, Hamburg, Germany) stadiometer with an accuracy of 0.1 cm.
6 month
Body Mass Index
大体时间:6 month
Participants' body mass indices (BMI) were calculated using the weight/height² formula (kg/m² ).
6 month

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)

2025年1月1日

初级完成 (实际的)

2025年6月1日

研究完成 (实际的)

2025年6月1日

研究注册日期

首次提交

2026年5月5日

首先提交符合 QC 标准的

2026年5月26日

首次发布 (实际的)

2026年5月29日

研究记录更新

最后更新发布 (实际的)

2026年5月29日

上次提交的符合 QC 标准的更新

2026年5月26日

最后验证

2025年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • BanirmaOnyediEylulU

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

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

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