Skip to main content
OpenTrials
Completed

NCT Number: NCT03000140

High-Intensity Interval Training on Pre-Hypertensive Subjects

Despite exercise training decrease blood pressure in 'average' terms, there is a wide interindividual variability after exercise training, being yet unknown what mode of exercise (e.g. endurance, strength, concurrent, or high intensity interval training) produce more/less non-responder (NR) prevalence (i.e., percentage of subjects who experienced a non-change/worsened response after training in some outcome).

Completed

Looking for future studies?

Notify Me

Key information

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Cristian Alvarez

Osorno, Chile

About this study

Despite exercise training decrease blood pressure in 'average' terms, there is a wide interindividual variability after exercise training, being yet unknown what mode of exercise (e.g. endurance, strength, concurrent, or high intensity interval training) produce more/less non-responder (NR) prevalence (i.e., percentage of subjects who experienced a non-change/worsened response after training in some outcome).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written informed consent;
  • Interested in improving health and fitness;
  • Systolic blood pressure > 120 mmHg and < 140 mmHg, and/or DBP ≥ 80 and < 90 mmHg according with standard classification;
  • No drug therapy during the previous 3 months;
  • Body mass index (BMI) 25 and 35 kg/m2); (c) physically inactive (according to the International Physical Activity Questionnaire previously validated in Chilean population)
  • Normal /mild altered lipid profile (total cholesterol [TC] ~200 and ≤250 mg/dL, low-density lipids [LDL-C] ~140 mg/dL and ≤200 mg/dL, high-density lipids [HDL-C] ≥20 and ~40 mg/dL, triglycerides ~150 and ≤250 mg/dL) according with standard classification.

Exclusion criteria

  • Cardiovascular contraindications to exercise histories of stroke;
  • Asthma and chronic obstructive pulmonary disease;
  • Musculoskeletal disorder such as low back pain;
  • Smokers in the last 3 months were not included in the study.

Treatment and study plan

High Intensity Interval Training

Behavioral

High Intensity Interval Training pre-hypertensive group; Exercise will be performed at three sessions per week. All sessions will be supervised by an exercise physiologist during 16 weeks.

Control Group

Behavioral

Moderade Intensity Interval Training pre-hypertensive group; Exercise will be performed at three sessions per week. All sessions will be supervised by an exercise physiologist during 16 weeks.

Primary outcomes

  1. Change from Baseline in systolic blood pressure and diastolic blood pressure

    Time frame: Baseline and 16 weeks immediately after the interventions ends

    After this, we calculated the delta changes in both variables and classified to all subjects in responders (R) and non-responders (NR) to decrease systolic or diastolic blood pressure.

Secondary outcomes

  1. Change from Baseline in body mass

    Time frame: Baseline and 16 weeks immediately after the interventions ends

  2. Change from Baseline in body mass index

    Time frame: Baseline and 16 weeks immediately after the interventions ends

    BMI will be calculated as the body weight in kilograms divided by the square of the height in meters.

  3. Change from Baseline in waist circumference

    Time frame: Baseline and 16 weeks immediately after the interventions ends

  4. Change from Baseline in fat mass

    Time frame: Baseline and 16 weeks immediately after the interventions ends

  5. Change from Baseline in heart rate at rest

    Time frame: Baseline and 16 weeks immediately after the interventions ends

    Baseline and 16 weeks immediately after the interventions ends

  6. Change from Baseline in fasting glucose

    Time frame: Baseline and 16 weeks immediately after the interventions ends

  7. Change from Baseline in lipids

    Time frame: Baseline and 16 weeks immediately after the interventions ends

    Lipid profile (low-density cholesterol, total cholesterol, high-density cholesterol and triglycerides)

  8. Change from Baseline in one maximum repetition strength test of leg-extension exercise

    Time frame: Baseline and 16 weeks immediately after the interventions ends

Sponsors and collaborators

Lead sponsor

Universidad Santo Tomas

Other

Collaborators

  • Healthcare Center Tomas Rojas
  • Universidad Pública de Navarra
  • Universidad del Rosario
  • University of Los Ríos

Registry information

Official study title

Health Status Factors Predicting Responses to Long-Term Training: Effects of 16-Week High-Intensity Interval Training on Pre-Hypertensive Subjects

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Dec 21, 2016
Registry last updated
Oct 11, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.