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Interval Versus Continuous Training in Healthy Adults

Effects of a High-intensity Interval Training Program Compared to a Moderate Intensity Program in Adults 18-44 Years

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02288403
Enrollment
44
Registered
2014-11-11
Start date
2015-04-30
Completion date
2016-06-30
Last updated
2016-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Keywords

Aerobic Exercise, Oxygen Consumption, Blood Pressure

Brief summary

Aerobic exercise produces increases in cardiorespiratory fitness (CF), which constitute a protective factor for cardiovascular disease and all-cause mortality. Therefore, aerobic exercise is a key strategy to promoting cardiovascular. There is some evidence that aerobic high intensity interval training may lead to greater increases in CF compared with continuous moderate-intensity training. The main objective of this study is to examine the effects of an aerobic high intensity training program versus a continuous moderate intensity training program on CF in men 18 to 44 years.

Detailed description

Forty-four individuals will be randomly assigned to one of two aerobic training programs on a treadmill. Both groups will performed three times a week for eight-weeks (on alternate days). Half will run 40 minutes of continuous exercise at an intensity between 65-75% of maximum heart rate, and the remaining 22 will complete 21.5 minutes of interval exercise at an intensity between 90-95% of maximum heart rate, with recoveries between 50-55 % of maximum heart rate. After each session both groups will complete eight strength exercises mainly including large muscle groups for two sets and 8-12 repetitions at an intensity equivalent to 60-70% of one repetition maximum (controlled by perceived effort). Rest between sets will be kept between 60 and 90 seconds. All participants will be evaluated at the start and completion of the intervention for their maximal oxygen consumption, blood pressure, waist circumference, BMI, body composition, and steps per week.

Interventions

Sponsors

Universidad de Antioquia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

* Perform aerobic exercise maximum 3 sessions per week

Exclusion criteria

* Currently participating in an aerobic high intensity training program * Smoker * History of cardiovascular disease * History of coronary heart disease * Arrhythmias * Heart failure/insufficiency * Hypertension * Diabetes * Under medical treatment with anticoagulants, beta-blockers, calcium antagonists, bronchodilators, and/or steroids * Psychological, neuromotor and/or osteo-muscular conditions that may affect participation in an exercise program.

Design outcomes

Primary

MeasureTime frame
Change in maximal oxygen uptakeBaseline and 8-weeks

Secondary

MeasureTime frame
Change in systolic blood pressureBaseline and 8-weeks
Change in diastolic blood pressureBaseline and 8-weeks

Countries

Colombia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026