- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06322459
Effect of Sport Education on Physical Fitness and Learning Attitude Among Junior High School Students
Effect of Football's Sport Education Curriculum as Intervention on Physical Fitness and Learning Attitude Among Junior High School Students in Hebei China
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Junlong Zhang, PHD
- Phone Number: 0397698153
- Email: zhangjunlong2413@gmail.com
Study Contact Backup
- Name: Soh Kim Geok, Professor
- Phone Number: 0397698153
- Email: kims@upm.edu.my
Study Locations
-
-
Hebei
-
Qinhuangdao, Hebei, China, 066000
- Recruiting
- The 19th Middle School
-
Contact:
- Junlong Zhang, PHD
- Phone Number: 0397698153
- Email: zhangjunlong2413@gmail.com
-
Contact:
- Gege Yao, Master
-
Principal Investigator:
- Junlong Zhang
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
The experimental subjects were students from two junior high schools in Haigang District, Qinhuangdao City, Hebei province. Before enrolling subjects, researchers need to inform them of the proposed study and what they need to participate in. After the subject is informed, the subject is allowed to ask questions. The various criteria and requirements for participation in this study were explained during the meeting. The criteria for inclusion of potential participants are as follows:
- Participants must be enrolled in junior high school and mixed gender.
- Participants must be in good health and capable of engaging in regular physical education activities.
- All participants and their parents have provided written informed consent for their involvement in the study.
Exclusion Criteria:
- Participants failing to complete all tests due to attendance-related issues (25%) or illness during experimental teaching or testing will be excluded.
- Participants who have already participated in the Sport Education Model will be excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Sport Eucation Curriculum
The Teaching experiment period of the Sport Education Model was 12 weeks, 40 minutes per lesson which included warm-up (10 minutes), basic content (20 minutes), rest of basic content (5 minutes), and cool-down (5 minutes).
|
The six characteristics of The Sport Education Model include season, affiliation, formal competition, culminating event, Record-keeping, and Festivity.
The intensity of the training is increasing in the first 30 minutes, and the intensity is gradually decreasing in the next 10 minutes.
|
Active Comparator: Normal Teaching
The Teaching experiment period of Normal Teaching was 12 weeks, 40 minutes per lesson which included warm-up (10-min), basic content (20min), rest of basic content (5min), and cool-down (5min).
Normal Teaching includes Teacher-directed learning (10 minutes) and Individual practice (10 minutes).
|
The intervention content, frequency, and intensity were the same as those in the experimental group, but the type of intervention was different.
The most significant difference between the two teaching methods lies in delivering basic content.
The Sport Education Model includes Teacher-directed learning (10 minutes) and Team practice (10 minutes); Normal Teaching includes Teacher-directed learning (10 minutes) and Individual practice (10 minutes).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cardiovascular fitness test
Time Frame: Pretest: before experiment; post-test1: end of 6 weeks; post-test2: end of 12 weeks
|
Equipment: Soccer field, cones, tape measure, Yo-Yo test software.
Procedure: Warm-up, group athletes, select appropriate mode, shuttle runs between cones with increasing speed, complete each run between beeps, record last completed run, measure total distance in meters (m).
|
Pretest: before experiment; post-test1: end of 6 weeks; post-test2: end of 12 weeks
|
Flexibility test
Time Frame: Pretest: before experiment; post-test1: end of 6 weeks; post-test2: end of 12 weeks
|
Equipment: Sit and reach box.
Procedure: Participant sits, feet against box, knees extended, bends forward reaching forward with fingertips, measure maximum range without sudden force, knees remain extended, retest if technical issues, measure in centimeters (cm).
|
Pretest: before experiment; post-test1: end of 6 weeks; post-test2: end of 12 weeks
|
Speed test
Time Frame: Pretest: before experiment; post-test1: end of 6 weeks; post-test2: end of 12 weeks
|
Equipment: Soccer field, tape measure, timing gates or stopwatch, cones or poles. Procedure: Thoroughly warm up, sprint 30 meters twice, record the best time, calculated in seconds (s). |
Pretest: before experiment; post-test1: end of 6 weeks; post-test2: end of 12 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Junlong Zhang, University Putra Malaysia
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- Junlong Zhang
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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