Effects of HIIT Integrated in PE Classes, on Physical Condition, Physical Activity and Motivation for Exercise

November 2, 2020 updated by: André Filipe Paulino da Silva Bento, University of Évora

Effects of a High-Intensity Interval Training Program Integrated in High-School Physical Education Classes, on Physical Condition, Physical Activity and Motivation for Exercise

Levels of activity and physical condition among adolescents are low, increasing the risk of chronic diseases. The most recent literature suggests that physical activity and physical condition are correlated with improved biopsychosocial variables of the young. The School and, concretely, the Physical Education classes are privileged spaces, promoters of positive changes for the rest of the life. HIIT is an efficient alternative to the invested time compared to aerobic training, being a powerful stimulus in improving cardiorespiratory performance, muscles oxidative capacity and sensitivity to insulin. This study intends to verify the effectiveness and feasibility in the implementation of HIIT in High-School Physical Education classes. The activity levels and physical condition of the adolescents will be evaluated and identified, before and after 16 weeks of implementation of the training program, as well as their effects on the motivation for the practice.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

274

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

      • Beja, Portugal, 7800
        • Escola Secundária D. Manuel I

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

15 years to 17 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Students enrolled in years 10-12

Exclusion Criteria:

  • Students will be ineligible if they do not provide parental consent to participate

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: HIIT Group
Two HIIT sessions delivered at the beginning of Physical education classes

The program will be applied in the first 10-15 minutes of each PE class, twice a week, including a brief warm-up, ranged from 14 to 20 intervals, adopting a 2:1 work to rest ratio (ie, 30-s work, followed by 30-s rest)

A cut-point of >=90% of maximal heart rate was used as our criterion for satisfactory compliance to high-intensity exercise

In order to estimate effort, fatigue and training load, a subjective effort scale will be used throughout each session. The heart rate will be monitored throughout the session in real time through Bluetooth technology.

Actigraph accelerometers (wGT3X-BT), randomly distributed by the students in each session, will be used to characterize the intensity of the sessions.

No Intervention: Control Group
Usual programmed Physical education classes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline Cardio-respiratory fitness at 4 months
Time Frame: 4 months
Assessed by Yo-Yo Intermitent Recovery Test 1(Tanner & Gore, 2014)
4 months
Change from 4 months Cardio-respiratory fitness at 6 months
Time Frame: 6 months
Assessed by Yo-Yo Intermitent Recovery Test 1(Tanner & Gore, 2014)
6 months
Change from baseline Muscular Strength at 4 months
Time Frame: 4 months
Assessed using push-up and curl-up tests (Plowman, 2013)
4 months
Change from 4 months Muscular Strength at 6 months
Time Frame: 6 months
Assessed using push-up and curl-up tests (Plowman, 2013)
6 months
Change from baseline Body Mass Index (BMI) at 4 months
Time Frame: 4 months
Assessed by Height and Weight (Dobbelsteyn, Joffres, MacLean, & Flowerdew, 2001)
4 months
Change from 4 months Body Mass Index (BMI) at 6 months
Time Frame: 6 months
Assessed by Height and Weight (Dobbelsteyn, Joffres, MacLean, & Flowerdew, 2001)
6 months
Change from baseline Physical Activity at 4 months
Time Frame: 4 months
Assessed by International Physical Activity Questionnaire (iPAQ), and accelerometry (Actigraph - wGT3X-BT)
4 months
Change from 4 months Physical Activity at 6 months
Time Frame: 6 months
Assessed by International Physical Activity Questionnaire (iPAQ), and accelerometry (Actigraph - wGT3X-BT)
6 months
Change from baseline Motivation at 4 months
Time Frame: 4 months
Assessed by Behavioral Regulation In Exercise Questionnaire (Cid et al., 2018).
4 months
Change from 4 months Motivation at 6 months
Time Frame: 6 months
Assessed by Behavioral Regulation In Exercise Questionnaire (Cid et al., 2018).
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: André Bento, University of Évora

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 16, 2019

Primary Completion (Actual)

October 15, 2019

Study Completion (Actual)

March 13, 2020

Study Registration Dates

First Submitted

July 10, 2019

First Submitted That Met QC Criteria

July 13, 2019

First Posted (Actual)

July 17, 2019

Study Record Updates

Last Update Posted (Actual)

November 3, 2020

Last Update Submitted That Met QC Criteria

November 2, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • SFRH/BD/136869/2018

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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