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Intervention in Habit, Automatic Affective Evaluations and Physical Activity Among University Students

NCT06140680 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2023-11-20

No results posted yet for this study

Summary

The goal of this clinical trial is to test the effectiveness of the LifelongU intervention in habit, automatic affective evaluation and physical activity among university students. The main questions aim to answer are:

* What is the difference in habit, automatic affective evaluation and physical activity between the intervention and control groups?
* What is the difference in habit, automatic affective evaluation and physical activity between the before and after intervention?

Participants will attend 12 sessions of four modules that performed face-to-face physical education lessons. Lesson content included 10-min health-related fitness knowledge, 30-min fitness test and training, 50-min motor skill training with behavior change techniques (90 min per a lesson, once a week).

Researchers will compare control group to see if any effect difference.

Conditions

  • Physical Inactivity
  • Sedentary Behavior

Interventions

BEHAVIORAL

LifelongU

The LifelongU intervention is an abbreviation name from LifelongU: Cultivating Physical Literacy for University \& Beyond. "LifelongU" is a unique and coined term that symbolizes the program's commitment to promoting physical literacy as a lifelong journey. It combines the words "Lifelong" and "University" to represent an intervention that focuses on physical literacy development not only during the university years but also throughout a person's entire life. The name is designed to convey the idea that physical literacy is an asset that will benefit individuals in all aspects of life, even after they leave the university.

BEHAVIORAL

Physical education

The control group received 12-week traditional physical education lesson as usual.

Sponsors & Collaborators

  • Universiti Sains Malaysia

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-02-12
Primary Completion
2024-05-17
Completion
2024-06-14

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06140680 on ClinicalTrials.gov