Effects of Microdosed Resistance Training During Physical Education on Health-Related Fitness in Adolescents

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15-18
SponsorWroclaw University of Health and Sport Sciences

About this trial

This study will examine whether short bouts of resistance training incorporated into physical education lessons can improve health-related physical fitness in secondary school students aged 15-16 years.

A total of 264 students will participate in two successive cohorts. School classes, rather than individual students, will be randomly assigned to study groups. In the first cohort, three resistance-training programs using low, moderate, or high training loads will be compared with usual physical education. The program producing the most consistent beneficial changes will then be tested in a new group of students in the second cohort and compared with usual physical education.

Each training program will last eight weeks. Participants will be assessed before the intervention, halfway through it, immediately after it, and eight weeks after it ends. Assessments will include body composition, blood pressure, cardiorespiratory fitness, muscular fitness, jumping performance, trunk muscular endurance, and sprint performance.

The study will evaluate both average changes in each group and the proportion of students showing improvements greater than the expected measurement error of the tests.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Enrollment in the second year of a participating secondary school.

Participation in regular physical education lessons at the participating school.

No health contraindications to physical exercise.

Written informed consent from the participant and, for participants who are minors, written informed consent from a parent or legal guardian.

Disqualifiers

Acute or chronic musculoskeletal injury preventing safe participation in the exercise intervention or physical fitness assessments.

Chronic disease or other medical condition constituting a contraindication to physical exercise.

Medical recommendation limiting participation in physical activity.

Acute infection or other temporary health condition preventing safe participation in a scheduled assessment.

Trial design

Design model

Sequential

Treatments tested in this trial

  • Resistance training microdosing during physical education

    Behavioral

    Teacher-supervised resistance training incorporated into physical education over eight weeks using body weight, dumbbells, medicine balls, and resistance bands. Cohort I compares three prescriptions: low-load (2-3 sets, 12-15 repetitions, 30-40 s rest, 3-4 repetitions in reserve), medium-load (3-4 sets, 8-12 repetitions, about 60 s rest, 2-3 repetitions in reserve), and high-load (4-5 sets, 6-8 repetitions, about 90 s rest, 1-2 repetitions in reserve). Progression occurs every two weeks through changes in repetitions, rest, external resistance, or sets. Cohort II receives the program selected from Cohort I based on the frequency of improvements exceeding minimal detectable change.

Treatment groups

264 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Group A: Cohort I: Low-Load Resistance TrainingExperimental treatment 1 intervention
Group B: Cohort I: Moderate-Load Resistance TrainingExperimental treatment 1 intervention
Group C: Cohort I: High-Load Resistance TrainingExperimental treatment 1 intervention
Group D: Cohort I: Usual Physical EducationNo intervention 0 interventions
Group E: Cohort II: Selected Resistance Training ProgramExperimental treatment 1 intervention
Group F: Cohort II: Usual Physical EducationNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Change in Body Fat Percentage

Body fat percentage will be assessed using bioelectrical impedance analysis. Measurements will be obtained at baseline, week 4, week 8, and week 16. Change from baseline at each post-baseline assessment will be analyzed and expressed in percentage points.

Time frame
Baseline, week 4, week 8, and week 16
2

Change in Muscle Mass

Muscle mass will be assessed using bioelectrical impedance analysis. Measurements will be obtained at baseline, week 4, week 8, and week 16. Change from baseline at each post-baseline assessment will be analyzed.

Time frame
Baseline, week 4, week 8, and week 16
3

Change in Systolic Blood Pressure

Systolic blood pressure will be measured after five minutes of seated rest. Three measurements will be obtained at each assessment, and the mean of the three measurements will be used for analysis. Change from baseline at each post-baseline assessment will be analyzed.

Time frame
Baseline, week 4, week 8, and week 16
4

Change in Diastolic Blood Pressure

Diastolic blood pressure will be measured after five minutes of seated rest. Three measurements will be obtained at each assessment, and the mean of the three measurements will be used for analysis. Change from baseline at each post-baseline assessment will be analyzed.

Time frame
Baseline, week 4, week 8, and week 16

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Wroclaw University of Health and Sport Sciences

Lead sponsor

Ministry of Science and Higher Education, Poland

Collaborator

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