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Effects of Short Duration High-intensity Interval Training on Peak Oxygen Consumption

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ClinicalTrials.gov Identifier: NCT04656509
Recruitment Status : Completed
First Posted : December 7, 2020
Last Update Posted : December 9, 2020
Sponsor:
Information provided by (Responsible Party):
University of Texas at Austin

Tracking Information
First Submitted Date  ICMJE October 12, 2020
First Posted Date  ICMJE December 7, 2020
Last Update Posted Date December 9, 2020
Actual Study Start Date  ICMJE April 1, 2019
Actual Primary Completion Date March 31, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: December 7, 2020)
  • 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.
  • 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.
Original Primary Outcome Measures  ICMJE
 (submitted: November 30, 2020)
  • Cardiovascular changes [ Time Frame: Pre and post training (8 weeks) ]
    Maximal oxygen consumption (VO2max) is an indicator of health and fitness. We measured VO2max with a graded exercise using electronically braked cycling ergometer.
  • Blood volume changes [ Time Frame: Pre and post training (8 weeks) ]
    Hematological variables can effect the performance of the people. We measured total blood volume, red blood cell volume, and plasma volume before and after training.
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: December 7, 2020)
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.
Original Secondary Outcome Measures  ICMJE
 (submitted: November 30, 2020)
Performance changes [ Time Frame: Pre and post training (8 weeks) ]
Our participants trained at maximal anaerobic power for 4-s. Therefore we measured maximal anaerobic power with different testing methods.
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Effects of Short Duration High-intensity Interval Training on Peak Oxygen Consumption
Official Title  ICMJE Effects of Short Duration High-intensity Interval Training on Peak Oxygen Consumption
Brief Summary 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.
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  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Cardiovascular Fitness
Intervention  ICMJE Other: 4-s sprint inertial load training
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.
Study Arms  ICMJE 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).
Intervention: Other: 4-s sprint inertial load training
Publications * Satiroglu R, Lalande S, Hong S, Nagel MJ, Coyle EF. Four-Second Power Cycling Training Increases Maximal Anaerobic Power, Peak Oxygen Consumption, and Total Blood Volume. Med Sci Sports Exerc. 2021 Dec 1;53(12):2536-2542. doi: 10.1249/MSS.0000000000002748.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: November 30, 2020)
11
Original Actual Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE April 24, 2020
Actual Primary Completion Date March 31, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

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.

-

Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years to 49 Years   (Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT04656509
Other Study ID Numbers  ICMJE 2019-01-0132
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE Not Provided
Current Responsible Party University of Texas at Austin
Original Responsible Party Same as current
Current Study Sponsor  ICMJE University of Texas at Austin
Original Study Sponsor  ICMJE Same as current
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Study Director: Edward F Coyle, Ph.D. University of Texas at Austin
PRS Account University of Texas at Austin
Verification Date December 2020

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP