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Clinical Trials/NCT06140680
NCT06140680
Recruiting
Not Applicable

The Effectiveness of the LifelongU Intervention in Habit, Automatic Affective Evaluations and Physical Activity Among University Students With Physical Inactivity

Universiti Sains Malaysia1 site in 1 country58 target enrollmentFebruary 12, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physical Inactivity
Sponsor
Universiti Sains Malaysia
Enrollment
58
Locations
1
Primary Endpoint
Habit
Status
Recruiting
Last Updated
2 years ago

Overview

Brief 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.

Detailed Description

A range of behavior change techniques derived from habit formation and self-regulation domain strategies will be used. These include behavioral rehearsal/practice, prompts/cues, and self-monitoring. The overall aim was to help students increase perceptions of physical competence and confidence, build positive affective attitude of physical activity, and develop autonomous association between physical activity and cues of time or events. Moreover, this intervention used student-centered learning strategies, game-centered approach in terms of mode of learning, and flexible in choice of timing, frequency, duration, and intensity of physical activity.

Registry
clinicaltrials.gov
Start Date
February 12, 2024
End Date
June 14, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dandan Huang

Phd Candidate

Universiti Sains Malaysia

Eligibility Criteria

Inclusion Criteria

  • aged 18-25 years
  • failure meeting the recommended physical activity guidelines (\< 150 minutes MVPA or \< 70 minutes VIPA in total a week) at the time of recruitment, screened via the Global Physical Activity Questionnaire

Exclusion Criteria

  • student athletes
  • the presence of health conditions that prevented safe engagement in physical activity, screened via the PAR-Q+.

Outcomes

Primary Outcomes

Habit

Time Frame: Assessments will be conducted at baseline (after the screening), 6th week after the baseline, 12th week, and 16th week.

Using questionnaire \[Physical activity self-report habit index\]: This is a 12-item questionnaire answered on a 7-point Likert scale ranging from 1 (Strongly disagree) to 7 (Strongly agree), with higher scores indicating stronger habit strength.

Physical Activity

Time Frame: Assessments will be conducted at baseline (after the screening), 6th week after the baseline, 12th week, and 16th week.

Using \[Global Physical Activity Questionnaire\]: the minimum time are 0 minutes per a day and maximum time are 1440 minutes per a day, and higher scores mean a better physical activity level.

Association Affective Evaluation

Time Frame: Assessments will be conducted at baseline (after the screening), 6th week after the baseline, 12th week, and 16th week.

Using \[Single-Category Implicit Association Test\]: the minimum value is 0 and maximum values is 5, and higher scores mean a positive affective attitude.

Study Sites (1)

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