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Cardiovascular Effects of High-Intensity Interval Training (HIIT)

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University of Delaware

Status

Completed

Conditions

Healthy Sedentary Adults With BP <140/90

Treatments

Behavioral: High-Intensity Interval Training
Behavioral: Moderate-Intensity Continuous Training

Study type

Interventional

Funder types

Other

Identifiers

NCT03602170
1009103-6

Details and patient eligibility

About

The purpose of this study is to determine the effect of high-intensity interval training (HIIT) in comparison to moderate-intensity continuous training (MCT) on blood pressure, blood vessel function, and blood pressure reactivity.

Full description

It is estimated that one-third of the adult population in the United States has blood pressure values that are classified as prehypertension. This slight elevation in blood pressure has been shown to result in an increased risk for developing hypertension and cardiovascular disease. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC7) recommends lifestyle modifications for individuals classified as prehypertensive. One lifestyle modification suggested by JNC7 is regular physical activity. Aerobic exercise, like moderate-intensity continuous training (MCT), has been shown to improve blood pressure, blood vessel function, and arterial stiffness in those with prehypertension. However, a major barrier to exercise adherence is the time commitment required. High-Intensity Interval Training (HIIT), which requires individuals to work at higher intensities for shorter durations, may offer an alternative training design that would reduce the time commitment. Previous studies have shown HIIT to be equal to or better at improving cardiorespiratory fitness and blood vessel function in multiple populations. Limited information is present on HIIT training in those with prehypertension. In this study, participants will be randomized into one of the two training program designs mentioned above (MCT or HIIT). Both programs will be completed over an 8-week period (3 sessions per week) and each training session will be supervised. Participants will complete testing visits before and after the training program to collect measures of cardiovascular health (exercise capacity, blood pressure, blood vessel function, and blood pressure reactivity). The goal is to compare the effects of the training programs on these measures of cardiovascular health.

Enrollment

20 patients

Sex

All

Ages

20 to 44 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Blood Pressure less than 140/90 mmHg
  • Sedentary

Exclusion criteria

  • Known or major signs/symptoms of cardiovascular, pulmonary, renal, or metabolic disease
  • Cancer
  • Use of antihypertensive medication
  • Current tobacco use
  • BMI (body mass index) less than 30 kg/m2
  • Postmenopausal
  • Current pregnancy
  • Current hormone replacement therapy
  • Participating in regular aerobic exercise at least three times a week for 30 minutes at a moderate intensity for the past 3 months or more
  • Not able to regularly exercise for any reason

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

High-Intensity Interval Training
Experimental group
Description:
8 weeks of high-intensity interval training. Three sessions per week will be performed (24 total sessions).
Treatment:
Behavioral: High-Intensity Interval Training
Moderate-Intensity Continuous Training
Active Comparator group
Description:
8 weeks of moderate-intensity continuous training. Three sessions per week will be performed (24 total sessions).
Treatment:
Behavioral: Moderate-Intensity Continuous Training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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