- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05744323
Effects of Functional Training on Fundamental Motor Skills Among Children
Effects of Functional Training on Fundamental Motor Skills Among Chinese Children Aged 6-7 Years Old in Tai Yuan
The goal of this clinical trial is to examine the effects that functional training may have on the development of fundamental motor skills and to create a systematic functional training program suitable for healthy children aged 6-7 years.
The main question[s] it aims to answer are:
- [To examine the effects of functional training on FMS among children aged 6-7 years.]
- [To compare the effects of functional training on FMS between boys and girls]
This study will include an experimental group and a control group. The experimental group will engage in functional training, while the control group will follow the state-mandated physical education curriculum. Through experiments, we will investigate the effect of functional training on children's fundamental motor skills and assess whether the experimental group's intervention effect is superior to the control group. The samples in this study were normal Chinese children aged 6-7 years. There were 40 people in both the experimental and control groups, including 20 boys and 20 girls
Study Overview
Detailed Description
Training intervention information This study will include an experimental group and a control group. The experimental group will engage in functional training, while the control group will follow the state-mandated physical education curriculum. Through experiments, we will investigate the effect of functional training on children's fundamental motor skills and assess whether the experimental group's intervention effect is superior to the control group. The samples in this study were normal Chinese children aged 6-7 years. There were 66 people in both the experimental group and control groups, including 35 boys and 35 girls.
Training Intervention Protocol for experiment group The selection of training items and content and the design of the training plan are based on the training content and principals involved in books such as the physical and motor function training for children, edited by Zhang Xiuli et al. (2018), the physical function training manual for adolescents and children edited by Wang Xiong (2019), and the functional training edited by Santana (2016). Furthermore, based on the literature review, the training frequency for the experiment was two (2) times a week, each lasting 45 minutes, including a 5-minute warm-up phase, a 35-minute main training phase, and a 5-minute relaxation phase, for a total training time of 12 weeks. The content was changed every two (2) weeks, and the intensity of the main phase of training ranged from 60% to 70%.
Training Intervention Protocol for control group The training content of the control group will be selected by the Compulsory Education Physical Education and Health Curriculum Standard in the year 2022. This standard follows the school's physical education teaching plan; the students in the control group will participate in the school's standard physical education curriculum. The specific content will be based on the actual physical education curriculum of the school. The training frequency for the control group was two times (2) a week, each lasting 45 minutes, and for a total training time of 12 weeks.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: ZHAN DONG, PHD
- Phone Number: (86)15034142244
- Email: brandondong001@gmail.com
Study Contact Backup
- Name: Kim Geok soh, Dr.
- Phone Number: (603)-9769 8153
- Email: kims@upm.edu.my
Study Locations
-
-
Shanxi
-
Taiyuan, Shanxi, China, 030012
- Wuyi Road Primary School, Taiyuan City, Shanxi Province, China
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Chinese Children in Taiyuan
- Primary school children are aged 6-7
- Including both gender boys and girls
Exclusion Criteria:
- Children cannot normally participate in regular physical education courses.
- The children have movement disorders.
- The children have physical or mental diseases.
- During the training period, the children have to do other sports training.
The procedure for selecting samples will make use of stratified sampling in addition to a random number table.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental group
The experimental group will engage in functional training
|
Physical and motor function training for children,may use BOSU balls, medicine balls, balance mats, fitness steps, and other training equipment to improve gradually
|
No Intervention: Control group
the control group will follow the state-mandated physical education curriculum.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Use the TGMD-2 scale to test locomotor skills
Time Frame: baseline, pre-intervention/Change from baseline locomotor skills at 12 weeks.
|
6 patterns tested within locomotor subtests.
The scoring is based on points listed for each pattern.
The total score is 24 points.
The athletic performance will be criterion-based scores compared with norm-referenced standards.
|
baseline, pre-intervention/Change from baseline locomotor skills at 12 weeks.
|
Use the TGMD-2 scale to test object control skills
Time Frame: baseline, pre-intervention/Change from baseline object control skills at 12 weeks.
|
6 patterns tested within object control subtests.
The scoring is based on points listed for each pattern.
The total score is 24 points.
The athletic performance will be criterion-based scores compared with norm-referenced standards.
|
baseline, pre-intervention/Change from baseline object control skills at 12 weeks.
|
Use the Y-test to test balance skill
Time Frame: baseline, pre-intervention/Change from baseline object balance skills at 12 weeks.
|
YBT requires children to balance on one leg whilst simultaneously reaching as far as possible with the other leg in three separate directions: anterior, posterolateral, and posteromedial.
The YBT composite score is calculated by summing the 3 reach directions and normalizing the results to the lower limb length.
All measurement scores were taken from scales on standing boards to the nearest 0.5 cm.
Distances can be read from the test equipment.
Each test was repeated three times, and the maximum range in each direction was recorded.
|
baseline, pre-intervention/Change from baseline object balance skills at 12 weeks.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Kim Geok soh, Universiti Putra Malaysia
Publications and helpful links
General Publications
- Baron J, Bieniec A, Swinarew AS, Gabrys T, Stanula A. Effect of 12-Week Functional Training Intervention on the Speed of Young Footballers. Int J Environ Res Public Health. 2019 Dec 24;17(1):160. doi: 10.3390/ijerph17010160.
- James, C. R. (2007). Functional Training for Athletes At All Levels.
- Boyle, M. (2004). Functional training for sports. Human Kinetics Publishers.
- Liebenson, C. (2014). Functional training handbook. Lippincott Williams & Wilkins.
- Heggond, M. S., Suresh, M. M., & Sundar, K. (2020). Impact of functional training on selected motor fitness components of sprinters. Journal of Xi'an University of Architecture & Technology, 12, 649-654.
- Kovac D, Krkeljas Z, Venter R. Effect of six-week traditional resistance and functional training on functional performance in female netball players. BMC Sports Sci Med Rehabil. 2022 Jan 15;14(1):10. doi: 10.1186/s13102-022-00402-8.
- Radcliffe, J. C. (2007). Functional training for athletes at all levels: workouts for agility, speed and power. Simon and Schuster.
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
Keywords
Other Study ID Numbers
- CN20230101
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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