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CompletedNCT05544370H2PEUpdated May 8, 2024

H2 Physical Education: Promoting Cardiometabolic Health by 2 High Intensity Intervallic Training Protocol, Twice a Week at Physical Education

An interventional study of Intensive high intensity intervallic training group and Extensive high-intensity intervallic training in Adolescent Behavior, sponsored by Universidad Católica San Antonio de Murcia. Completed at 1 site in Spain. Open to participants aged 12 Years to 14 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-05-08.

Sponsored by Universidad Católica San Antonio de Murcia · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Randomized
Ages
12 Years to 14 Years
Sex
All
01

Study summary

Several risk factors associated with cardiovascular disease could be prevented or treated by means of physical activity from childhood. Among the physical exercise programs for the improvement of these variables we can highlight high-intensity interval training. However, most of these studies have been carried out on overweight or obese athletes or schoolchildren and existing protocols on high intensity intervallic training are different. The main objective of the present research is to compare two high-intensity intervallic training protocols on body composition, heart rate, blood pressure, lipid profile, blood glucose, cardiovascular fitness, strength, quality of life, physical activity, enjoyment of physical activity and accident proneness in adolescents. The present investigation will be elaborated by a randomized-control trial design, with 2 experimental groups and a control group (CG). In each experimental groups a different protocol of high-intensity interval training is applied.

It is assessed cardiovascular capacity and strength. Body composition is assessed. Heart rate and blood pressure were also recorded. Lipid profile and blood glucose were obtained by blood sampling. Quality of life, sedentary and physical activity lifestyle, enjoyment of physical activity and Psychoeducational factors determining accident process are assessed.

Read the detailed description

Cardiovascular diseases are the leading cause of death today. These have been inversely correlated with physical activity and fitness in adults, children and adolescents. In this sense, certain risk factors associated with cardiovascular disease could be prevented or treated by means of physical activity from childhood. Traditionally, the benefits of physical activity on cardiovascular markers and physical fitness in children and adolescents have been described in research conducted with traditional aerobic exercise programs. Among the physical exercise programs for the improvement of these variables we can highlight high-intensity interval training. However, most of these studies have been carried out on overweight or obese athletes or schoolchildren. On the other hand, the existing protocols on high intensity intervallic training are different, there have been intensive and extensive protocols. Likewise, the investigations do not usually control the real intensity of work and it has been described that in most cases the participants do not manage to reach the described intensity, which indicates that they are not working at the level that is considered or they are working with an intensity of an extensive protocol while the duration is of an intensive protocol. In this sense, the objective of the present research is a) to know the effect of high intensity intervallic training on body composition, heart rate, blood pressure, lipid profile, glycemia, cardiovascular capacity, strength, quality of life, physical activity, enjoyment of physical activity and accident proneness in adolescents and b) to compare two high-intensity intervallic training protocols on body composition, heart rate, blood pressure, lipid profile, blood glucose, cardiovascular fitness, strength, quality of life, physical activity, enjoyment of physical activity and accident proneness in adolescents.

The present investigation will be elaborated by a randomized-control trial design, with 2 experimental groups and a control group (CG); with pre-test and post-test. Each experimental groups performance differences protocol of high-intensity interval training.

The inclusion criteria will be: a) being in Compulsory Secondary Education; b) not presenting any musculoskeletal, neurological, cardiological, metabolic, rheumatic or previous history of spinal pathologies or with previous treatment; c) be active in the sessions of Physical Education.

Primary outcome measure are cardiovascular capacity, strength of upper limbs and strength of lower limbs. These variables are tested with "Course Navette test", handgrip dynamometry and long jump test, respectively.

Secondary outcome measure are body composition and its assessed by height, weight, waist circumference, fat percentage, hydration, muscle mass, bone weight and visceral fat. The body mass index will be obtained by recording weight and height (BMI = Weight (kg) / height (cm) 2). Heart rate and blood pressure were also recorded. Lipid profile (high density lipoproteins, low density lipoproteins and triglycerides) and blood glucose were obtained by blood sampling. Quality of life are assessed through the "Kidscreen-27 questionnaire". The sedentary lifestyle as well as the level of physical activity will be evaluated through the Adolescent International Physical Activity Questionnaire (IPAQ).

The enjoyment of physical activity and a questionnaire on Psychoeducational factors determining accident proneness in adolescents were assessed.

Intensity was assessed during all sessions by means of a heart rate monitor for each adolescent.

The type of activity used to develop the training was continuous running. After the usual warm-up in physical education classes, one of the two high-intensity interval training protocols was applied. Both have the same work time but distributed in different ways and with different intensities.

The intensive high intensity intervallic training group performs 6 sets of 60 seconds of work and 60 seconds of rest. During the first two weeks we work at an intensity of 80-85% of the reserve heart rate during the work phase and 50-55% of the reserve heart rate during the rest time. In weeks 3 and 4 the intensity in the work phase is increased by 5%, reaching from the fifth week onwards a work intensity of 95-95% of the reserve heart rate.

The extensive high-intensity intervallic training group performs 3 sets of 120 seconds of work and 120 seconds of rest at an intensity of 70-75% of the reserve heart rate during the work phase and an intensity of 50-55% of the reserve heart rate during the rest phase. In weeks 3 and 4 the intensity in the work phase is increased by 5%, reaching from the fifth week onwards a work intensity of 80-85% of the reserve heart rate.

The program duration is 8 weeks and the frequency of intervention is 2 sessions per week.

02

Conditions studied

  • Adolescent Behavior

Keywords

  • adolescents
  • cardiovascular
  • strength
  • high intensity interval training
  • metabolic syndrome
  • physical activity
03

In context

Lead sponsor

Universidad Católica San Antonio de Murcia is the lead sponsor of 132 studies on the registry; 18 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 14 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • being in Compulsory Secondary Education
  • be active in the sessions of Physical Education

Exclusion criteria

Exclusion Criteria:

  • presenting any musculoskeletal, neurological, cardiological, metabolic, rheumatic or previous history of spinal pathologies or with previous treatment
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
85 participants (actual)

Study arms

  • Experimental
    Intensive high intensity intervallic training group

    The intensive high intensity intervallic training group performs 6 sets of 60 seconds of work and 60 seconds of rest. During the first two weeks we work at an intensity of 80-85% of the reserve heart rate during the work phase and 50-55% of the reserve heart rate during the rest time. In weeks 3 and 4 the intensity in the work phase is increased by 5%, reaching from the fifth week onwards a work intensity of 95-95% of the reserve heart rate. The program duration is 8 weeks and the frequency of intervention is 2 sessions per week.

    Behavioral: Intensive high intensity intervallic training group

  • Experimental
    Extensive high-intensity intervallic training group

    The extensive high-intensity intervallic training group performs 3 sets of 120 seconds of work and 120 seconds of rest at an intensity of 70-75% of the reserve heart rate during the work phase and an intensity of 50-55% of the reserve heart rate during the rest phase. In weeks 3 and 4 the intensity in the work phase is increased by 5%, reaching from the fifth week onwards a work intensity of 80-85% of the reserve heart rate. The program duration is 8 weeks and the frequency of intervention is 2 sessions per week.

    Behavioral: Extensive high-intensity intervallic training

  • No intervention
    Control group

    The control group will carry out their usual physical education classes which consist of games, jumping, moving, balance and different sports.

Interventions

  • BehavioralIntensive high intensity intervallic training group

    The intensive high intensity intervallic training group performs 6 sets of 60 seconds of work and 60 seconds of rest. During the first two weeks we work at an intensity of 80-85% of the reserve heart rate during the work phase and 50-55% of the reserve heart rate during the rest time. In weeks 3 and 4 the intensity in the work phase is increased by 5%, reaching from the fifth week onwards a work intensity of 95-95% of the reserve heart rate. The program duration is 8 weeks and the frequency of intervention is 2 sessions per week.

  • BehavioralExtensive high-intensity intervallic training

    The extensive high-intensity intervallic training group performs 3 sets of 120 seconds of work and 120 seconds of rest at an intensity of 70-75% of the reserve heart rate during the work phase and an intensity of 50-55% of the reserve heart rate during the rest phase. In weeks 3 and 4 the intensity in the work phase is increased by 5%, reaching from the fifth week onwards a work intensity of 80-85% of the reserve heart rate. The program duration is 8 weeks and the frequency of intervention is 2 sessions per week.

06

What researchers measure

Primary outcomes

  1. Change to baseline to 8 week of Cardiovascular capacity

    Cardiovascular capacity is evaluated by means of the Course Navete test. A high value in this test refers to a better cardiovascular capacity.

    Time frame: Two times. Baseline and 8 week later

  2. Change to baseline to 8 week of Manual clamping force

    Manual grip strength is assessed by means of dynamometry. The higher the value in this test, the greater the manual grip strength. It is recorded in kilograms.

    Time frame: Two times. Baseline and 8 week later

  3. Change to baseline to 8 week of Long jump

    The long jump is recorded by means of a mobile application. A higher value in this test reflects greater strength in the lower extremities. It is recorded in centimeters.

    Time frame: Two times. Baseline and 8 week later

Secondary outcomes

  1. Change to baseline to 8 week of Height

    The size of the subject will be measured in centimeters.

    Time frame: Two times. Baseline and 8 week later

  2. Change to baseline to 8 week of Weight

    The Weight of the subject will be measured in kilograms.

    Time frame: Two times. Baseline and 8 week later

  3. Change to baseline to 8 week of Waist circumference

    The waist circumference of the subject will be measured in centimeters.

    Time frame: Two times. Baseline and 8 week later

  4. Change to baseline to 8 week of Fat percentage

    The percentage of fat was assessed by bioimpedance.

    Time frame: Two times. Baseline and 8 week later

  5. Change to baseline to 8 week of Hydration percentage

    The hydratation was assessed by bioimpedance.

    Time frame: Two times. Baseline and 8 week later

  6. Change to baseline to 8 week of Muscle mass

    The muscle mass was assessed by bioimpedance. It was register in kilograms.

    Time frame: Two times. Baseline and 8 week later

  7. Change to baseline to 8 week of Bone weight

    The bone weight was assessed by bioimpedance. It was register in kilograms.

    Time frame: Two times. Baseline and 8 week later

  8. Change to baseline to 8 week of Visceral fat

    The visceral fat was assessed by bioimpedance. It was register in kilograms.

    Time frame: Two times. Baseline and 8 week later

  9. Change to baseline to 8 week of Heart rate

    The heart rate is taken under a blood pressure and heart rate device and the value is given in number of beats per minute.

    Time frame: Two times. Baseline and 8 week later

  10. Change to baseline to 8 week of systolic and diastolic Blood pressure

    Blood pressure (systolic and diastolic) is taken under a blood pressure and heart rate measuring device and the value is given in number of millimeters of mercury.

    Time frame: Two times. Baseline and 8 week later

  11. Change to baseline to 8 week of Blood glucose

    Blood glucose lipoproteins is analyzed by blood extraction.

    Time frame: Two times. Baseline and 8 week later

  12. Change to baseline to 8 week of High density lipoproteins

    High-density lipoproteins is analyzed by blood extraction.

    Time frame: Two times. Baseline and 8 week later

  13. Change to baseline to 8 week of Low density lipoproteins

    Low-density lipoproteins is analyzed by blood extraction.

    Time frame: Two times. Baseline and 8 week later

  14. Change to baseline to 8 week of Triglycerides

    Triglycerides is analyzed by blood extraction.

    Time frame: Two times. Baseline and 8 week later

  15. Change to baseline to 8 week of Quality of life level

    Quality of life was assessed through the "Kidscreen-27 questionnaire" (assess health and subjective well-being in children and adolescents). This questionnaire report a score on a scale, with 5 option (never, a little, often, very often and always). The minimum value is 0 up to 100. A higher score on this test reflects a higher quality of life level. Higher score mean a better outcome.

    Time frame: Two times. Baseline and 8 week later

  16. Change to baseline to 8 week of Sedentary and physical activity lifestyle

    The sedentary lifestyle as well as the level of physical activity will be evaluated through the Adolescent International Physical Activity Questionnaire (IPAQ).

    Time frame: Two times. Baseline and 8 week later

  17. Change to baseline to 8 week of Enjoyment of physical activity

    The enjoyment of physical activity was measure by a questionaire. This questionnaire report a score on a scale, with 5 option (strongly disagree, somewhat disagree, neutral, somewhat agree and strongly agree). The minimum value is 0 up to 100. A higher score on this test reflects a higher enjoyment. Higher score mean a better outcome.

    Time frame: Two times. Baseline and 8 week later

  18. Risk of Accident level

    Psychoeducational factors determining accident proneness in adolescents were assessed by questionaire. A higher score on this test reflects a higher risk of an adolescent accident. The questionnaire is composed of 4 factors. Factor 1. Perceived competence (from 8 to 48 points); Factor 2. Factor 3. Competitiveness (from 4 to 24 points), Factor 4. Risk-taking (from 4 to 24 points); and Factor 5. A higher score mean a high point in the factor.

    Time frame: 8 week

07

Study locations

1 site
  • Noelia G González-Gálvez, PhD.
    Murcia, 30010, Spain
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05544370
Lead sponsor
Universidad Católica San Antonio de Murcia
Responsible party
Noelia González-Gálvez (Principal investigator, Universidad Católica San Antonio de Murcia) — Principal investigator
First posted
Sep 16, 2022
Start date
Sep 12, 2022
Primary completion
Oct 30, 2022
Completion
Dec 30, 2022
Last update
May 8, 2024

Study contacts

NOELIA GONZALEZ GALVEZ, PhD
principal investigator · UCAM

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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