- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06834620
School-Based Physical Education Program and Its Effects on Motor Fitness in Malaysian Children (SPEP-FIT)
February 13, 2025 updated by: Gerasimos Grivas, Hellenic Naval Academy
Impact of a Novel Primary School-based Physical Education Program on Physical and Motor Fitness of Malaysian Children: a Randomized Controlled Trial
The objective of this randomized controlled trial was to compare the effects of a standard school physical education program (SPEP) and a rhythmic and gymnastic activities-based school physical education program (RGPEP) on the physical and motor fitness parameters of Malaysian primary school children.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This randomized controlled trial evaluates the impact of two distinct physical education programs on the physical and motor fitness of Malaysian primary school children.
The intervention group participates in a rhythmic and gymnastic activities-based physical education program (RGPEP), designed to enhance balance, coordination, flexibility, and agility through structured, progressive activities.
The control group follows the standard school physical education program (SPEP) in line with the national curriculum, which emphasizes general fitness and physical activity without specific rhythmic or gymnastic components.
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Children aged 8 years at the time of enrollment.
- Both boys and girls.
- Regular school attendance during the academic year.
- No diagnosed health conditions or chronic diseases that could interfere with physical activity.
- Not involved in extracurricular sports activities outside the school environment.
- Not engaged in extra traveling to and from school on foot or by bicycle.
- Parents or legal guardians provided written informed consent.
- The child provided verbal assent to participate in the study.
Exclusion Criteria:
- Children missing more than 20% of scheduled physical education classes.
- Overweight children with a BMI ≥ 23 kg/m².
- Underweight children with a BMI < 18.5 kg/m².
- Children involved in regular sports training or participation in extracurricular sports activities during the intervention period.
- Children with any pre-existing medical conditions or injuries that could limit participation in physical activities.
- Children with developmental or motor impairments affecting their ability to perform the required fitness activities.
- Children on any medication that could interfere with their performance or physical fitness evaluation.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Rhythmic and Gymnastics-Based Exercise Group
Participants in this arm received 80 sessions of a Rhythmic and Gymnastics-Based Physical Education Program (RGPEP) over an academic year.
The program focused on rhythmic skills, gymnastics patterns, and movement-based activities designed to enhance motor and physical fitness.
|
A structured, year-long school-based physical education program integrating rhythmic movements, gymnastics, and small equipment exercises designed to enhance motor and physical fitness.
The program included 80 sessions (two per week) focusing on rhythmic activities such as twisting, partner balance, animal walks, tumbling, and rope exercises.
The intervention aimed to improve strength, flexibility, agility, and cardiovascular endurance compared to traditional physical education classes.
|
|
Active Comparator: Control group
Participants in this arm followed the standard Malaysian school physical education curriculum, which included 60 minutes of physical education and 30 minutes of health education per week, as prescribed by the Malaysian Ministry of Education.
|
A structured, year-long school-based physical education program integrating rhythmic movements, gymnastics, and small equipment exercises designed to enhance motor and physical fitness.
The program included 80 sessions (two per week) focusing on rhythmic activities such as twisting, partner balance, animal walks, tumbling, and rope exercises.
The intervention aimed to improve strength, flexibility, agility, and cardiovascular endurance compared to traditional physical education classes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Standing Broad Jump
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
The standing broad jump test measures lower body power in centimeters.
Participants will perform a jump from a standing position, and the longest distance recorded will be used for analysis.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
20-Meter Sprint
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Sprint speed will be assessed using a 20-meter sprint test.
The time taken (in seconds) to complete the distance will be recorded.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
4 × 10-Meter Shuttle Run
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Agility and speed will be measured using a 4 × 10-meter shuttle run test.
Time to complete the test (in seconds) will be recorded.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
Push-Ups
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Upper body endurance will be assessed using the push-up test.
The number of correctly executed push-ups performed will be recorded.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
Sit and Reach Test
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Flexibility will be assessed using the sit and reach test.
The maximum reach distance (in centimeters) will be recorded.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
Multistage Shuttle Run Test
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Cardiovascular endurance will be measured using the multistage shuttle run test.
VO₂max (mL/kg/min) will be estimated based on performance.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Height
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Standing height will be measured using a stadiometer and recorded in centimeters.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
Weight
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
Body weight will be measured using a digital scale and recorded in kilograms.
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
|
Body Mass Index
Time Frame: Baseline (Month 0) and Post-Intervention (Month 12).
|
BMI will be calculated as weight (kg) divided by height squared (m²).
|
Baseline (Month 0) and Post-Intervention (Month 12).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 14, 2015
Primary Completion (Actual)
February 14, 2016
Study Completion (Actual)
February 14, 2016
Study Registration Dates
First Submitted
February 9, 2025
First Submitted That Met QC Criteria
February 13, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 13, 2025
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hellenic Naval Academy
- PNURSP2025R424 (Other Grant/Funding Number: Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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