- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04656509
Effects of Short Duration High-intensity Interval Training on Peak Oxygen Consumption
December 7, 2020 updated by: University of Texas at Austin
High-intensity interval training (HIIT) is an effective tool to improve cardiovascular fitness and maximal anaerobic power.
Different methods of HIIT have been studied but the effect of a maximal effort cycling and very short exercise time (i.e., 4-s) with short recovery time (15-30 s) and a high number of repetitions (i.e., 30 bouts) is unknown.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The investigators examined the effects of training at maximal anaerobic power during cycling (PC) on maximal anaerobic power, peak oxygen consumption (VO2peak), and total blood volume in 11 young healthy individuals (age: 21.3±0.5 y) (6 men, 5 women).
Methods: Participants trained three times a week for eight weeks performing a PC program consisting of 30 bouts of 4-s at an all-out intensity (i.e., 2 minutes of exercise per session).
The cardiovascular stress progressively increased over the weeks by decreasing the recovery time between sprints (30 to 24 to 15-s) and thus session time decreased from 17 to < 10 min.
Study Type
Interventional
Enrollment (Actual)
11
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
-
-
Texas
-
Austin, Texas, United States, 78712
- Human Performance Laboratory, Department of Kinesiology and Health Education, the University of Texas at Austin
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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
18 years to 49 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Young (18-30), Healthy, Recreationally active, but untrained (not meeting ACSM's recommendations of 150 min/week of moderate-vigorous aerobic exercise) -
Exclusion Criteria:
Cardiovascular disease Smoking Subjects who were exercising regularly (>75 min/week) were excluded.
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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: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 4-s sprint inertial load training
Participants trained three times a week for eight weeks following the training program consisting of 30 bouts of 4s all-out cycling on an inertial-load ergometer with progressively decreasing recovery time (30 to 24 to 15s).
|
A program employing 30 bouts of 4s inertial load sprint training with progressively reduced recovery time (30 to 15 s) between sprints is effective for improving blood volume, VO2peak and maximal power.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cardiovascular changes
Time Frame: Pre and post training (8 weeks)
|
Maximal oxygen consumption (VO2max) is an indicator of health and fitness.
The investigators measured VO2max with a graded exercise using electronically braked cycling ergometer.
|
Pre and post training (8 weeks)
|
|
Blood volume changes
Time Frame: Pre and post training (8 weeks)
|
Hematological variables can effect the performance of the people.
The investigators measured total blood volume, red blood cell volume, and plasma volume before and after training.
|
Pre and post training (8 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Performance changes
Time Frame: Pre and post training (8 weeks)
|
Study participants trained at maximal anaerobic power for 4-s.
Therefore, the investigators measured maximal anaerobic power with different testing methods.
|
Pre and post training (8 weeks)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Edward F Coyle, Ph.D., University of Texas at Austin
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
April 1, 2019
Primary Completion (Actual)
March 31, 2020
Study Completion (Actual)
April 24, 2020
Study Registration Dates
First Submitted
October 12, 2020
First Submitted That Met QC Criteria
November 30, 2020
First Posted (Actual)
December 7, 2020
Study Record Updates
Last Update Posted (Actual)
December 9, 2020
Last Update Submitted That Met QC Criteria
December 7, 2020
Last Verified
December 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- 2019-01-0132
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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