- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07402304
The Cultivation of College Students' Social Behavior in Public Physical Education Courses in Colleges and Universities: A Study Based on the Experiential Learning Model
February 6, 2026 updated by: Han Xu
This study adopts a quasi-experimental design and plans to recruit 94 university students from a university in Jiangsu Province, randomly divided into an experimental group and a control group.
The experimental group will receive tennis courses based on the experiential learning model, with one 90-minute class each week.
The course content will combine tennis skill training and social interaction activities that promote cooperation.
The control group will continue with conventional tennis teaching.
The study will include baseline testing, teaching intervention, and post-intervention assessment.
The main measurement indicators will include prosocial behavior and physical fitness.
Prosocial behavior will be evaluated using the PABSS Chinese version questionnaire, which includes aspects such as prosocial behavior toward teammates and opponents, antisocial behavior, and teamwork spirit.
Physical fitness will be assessed using the physical fitness test and the CAPL-2 Chinese version questionnaire.
Independent samples t-test, paired samples t-test, two-way analysis of variance (ANOVA), and analysis of covariance (ANCOVA) will be used to analyze the differences in prosocial behavior and physical fitness between the experimental and control groups.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
94
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Jiangsu
-
Yangzhou, Jiangsu, China, 225000
- Yangzhou University
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Participants are university students aged between 18 and 22 years who are capable of safely participating in physical activities and have no health risks.
- Students must be able to communicate effectively, understand, and sign the informed consent form.
- Students must be willing to participate in an 8-week intervention (once a week, 90 minutes per session) and be able to withdraw from the study at any time.
- Participants must be able to complete all the teaching activities and have no physical or psychological conditions that limit their full participation in physical activities.
- All participants are from the agreed university in Jiangsu to ensure consistency in the environment and reduce external interference.
- All participants must agree to follow the study rules and participate in the research.
Exclusion Criteria:
- Students with physical or psychological health conditions that prevent safe participation in physical activities.
- Students who are unable to communicate effectively or cannot understand the informed consent form.
- Students who are unable to attend the full 8-week intervention (once a week, 90 minutes per session).
- Students who withdraw from the study or do not complete the course during the research period.
- Students with serious illnesses or health risks will be excluded from the study.
- Factors such as family socio-economic status, academic performance, or participation in physical activities that could potentially affect the results will be used as exclusion criteria.
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group: Tennis Course Based on Experiential Learning Model
The experimental group will participate in a tennis course based on the experiential learning model.
The course will involve 90-minute weekly sessions, focusing on tennis skill development and social interaction activities designed to promote cooperation and enhance prosocial behavior among students.
This intervention aims to foster teamwork, social responsibility, and collective spirit through sports.
|
The intervention in this study consists of a tennis course based on the experiential learning model, with one 90-minute class per week.
The course includes tennis skill training and social interaction activities that promote cooperation.
Compared to conventional physical education courses, this course focuses on enhancing students' collectivism and social responsibility through cooperation and competition in sports.
|
|
Active Comparator: Control Group: Regular Tennis Course
The control group will continue with the regular tennis course, focusing solely on tennis skill development without incorporating the experiential learning model.
The course will follow the standard physical education curriculum without additional social interaction activities aimed at enhancing prosocial behavior or cooperation.
|
The control group will continue with the regular tennis course, focusing solely on tennis skill development without incorporating the experiential learning model.
The course will follow the standard physical education curriculum without additional social interaction activities aimed at enhancing prosocial behavior or cooperation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prosocial Behavior in University Students After Tennis Course Based On The Experiential Learning Model Intervention
Time Frame: The intervention will last for 8 weeks, with one 90-minute session each week, and outcomes will be measured at the baseline, at the post-intervention stage
|
The primary outcome measure is the improvement in prosocial behavior of university students who participated in the tennis course based on the experiential learning model.
This will be assessed through the PABSS Chinese version questionnaire , focusing on teamwork, cooperation, social responsibility,
|
The intervention will last for 8 weeks, with one 90-minute session each week, and outcomes will be measured at the baseline, at the post-intervention stage
|
|
Physical Literacy in University Students After Experiential Learning-Based Tennis Course"
Time Frame: The physical literacy outcomes will be measured at the baseline and post-intervention stage (week 8).
|
The primary outcome measure for physical literacy is the improvement in students' overall physical health and fitness after participating in the tennis course based on the experiential learning model.
The CAPL-2 Chinese version questionnaire will be used to assess physical literacy based on various aspects of physical health and fitness.
|
The physical literacy outcomes will be measured at the baseline and post-intervention stage (week 8).
|
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)
September 25, 2025
Primary Completion (Actual)
December 12, 2025
Study Completion (Actual)
December 12, 2025
Study Registration Dates
First Submitted
February 2, 2026
First Submitted That Met QC Criteria
February 6, 2026
First Posted (Actual)
February 11, 2026
Study Record Updates
Last Update Posted (Actual)
February 11, 2026
Last Update Submitted That Met QC Criteria
February 6, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- YXYLL -2025- 120
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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