- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05039294
The Effect Of A School-Based Physical Activity Educational Program
The Effect Of A School-Based Physical Activity Educational Program On Adolescents' Physical Activity-related Knowledge, Performance, And Self-Efficacy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Regular physical activity of different intensity has many significant benefits on the health of all ages, particularly adolescents. School-based educational programs about physical activity were found to increase the level of physical activity among adolescents positively. However, among adolescents in Jordan, few studies measured the impact of school-based educational programs on students' level of physical activity and knowledge, and there is no single study that measured the students' physical activity self-efficacy.
Aim: To assess the effectiveness of a school-based physical activity program on adolescents' knowledge of physical activity, physical performance, and physical self-efficacy.
Methods: A Randomized Control trial (RCT) design was used among 210 8th grade school students (boys and girls) from four governmental schools in North of Jordan during December and January. Physical Activity Questionnaire for older children (PAQ-C) scales, Physical self-efficacy scale, and Knowledge of Physical Activity scale were used to collect students' data. The duration of the educational program was four weeks, with a total of 7 hours. Ethical approval was approached from the Committee on Human Subjects Research at Jordan University of Science and Technology and the Ministry of Education before the data collection.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Irbid, Jordan, 22110
- Nahla M. Al Ali
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- all students boys and girls in 8th grade from selected schools affiliated with eight educational directorates of the Irbid governorate,
- who are ready to participate in the educational program and meet the inclusion criteria.
Exclusion Criteria:
- Students who have any medical problems (asthma, diabetes, cardiac problems) and physical disabilities were excluded.
Study Plan
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 |
|---|---|
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Experimental: intervention
provided the educational programs with all contents, and follow up after one month
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The structure of the educational sessions includes physical education lectures, group discussions, videos, training sessions, physical activities diaries, short quizzes, and feedback after each session.
The educational programs were conducted among students with intervention groups at two-level individually and in school.
The individual-level includes classroom lectures that mainly emphasized the health benefits of physical activity and provided necessary information about physical activity fitness for 60 minutes and were given weekly for four weeks.
In coordination with the school sports teacher, training sessions included moderate to vigorous physical activities for 45 minutes twice weekly for four weeks
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No Intervention: control
received no intervention, but assessed pre-post
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Knowledge
Time Frame: baseline pre-intervention, and immediately after the intervention
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Adolescents' Physical Activity-Related Knowledge: This section was developed by the researcher based on previous literature.
The questionnaire contained eighteen questions to assess student knowledge about the definition of physical activity, exercise, health, and physical fitness.
Types of physical activity, physical activity benefits, and negative consequences of physical inactivity on health, and recommendation.
Each of the eighteen items has three alternatives: true, false, and do not know.
The total knowledge score was used based on the percentages of the correctly answered questions.
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baseline pre-intervention, and immediately after the intervention
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physical activity level
Time Frame: baseline pre-intervention, and immediately after the intervention
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Physical activity performance: Physical Activity Questionnaires for older children (PAQ-C) is used to assess moderate to vigorous physical activity levels over the past 7 days (Crocker et al.,1997).
It includes eight questions, each one scored on 5 point scale.
Item 1 (Spare time activity) takes the mean of all activities ("no" activity being a 1, "7 times or more" being a 5) on the activity checklist to form a composite score for item 1. Items 2 to 8 (PE, recess, lunch, right after school, evening, weekends, and describes you best), the answers reflect the level of physical activity for each item from lowest activity response to the highest activity response.
Then used the reported value is determined for each item (the lowest activity response being a 1 and the highest activity response being a 5).
Item 9 reflects the mean of physical activity during the week ("none" being a 1, "very often" being a 5) to form a composite score for item 9
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baseline pre-intervention, and immediately after the intervention
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self-efficacy
Time Frame: baseline pre-intervention, and immediately after the intervention
|
physical activity self-efficacy":The final validated modified version of the physical activity self-efficacy scale adolescent's protocol questionnaire (Motl et al., 2000) consists of 8 items used in this study to measure physical activity self-efficacy.
The scale contains two sections: self-management and social support.
Self-management of the physical activity section consists of 6 items related to cognitive and behavioral factors that may increase or decrease physical activity participation.
Social support was measured by two items which are support from family and friends.
The students were asked to choose from 5 items on a Likert scale.
The scoring ranged from 1 (disagree a lot) to 5 (agree a lot).
The total score of both sections ranged from 8- 40, higher scores indicate higher self-efficacy.
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baseline pre-intervention, and immediately after the intervention
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Collaborators and Investigators
Investigators
- Principal Investigator: Nahla M. Al Ali, Jordan University of Science and Technology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- 20200023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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