Rest Time on Gain Aerobic and Anaerobic Performance (Performance)

December 25, 2015 updated by: Alberto Souza de Sá Filho, Universidade Federal do Rio de Janeiro

Can The Rest Interval Time Provide Superior Gains on VO2max, Aerobic and Anaerobic Performance Obtained With High Intensity Interval Training (HIIT)? a Randomized Controlled Study

Based on studies of high intensity interval training (HIIT) in the literature, higher gains in VO2max and performance are obtained in short periods of training time. However, different designs training configurations, for example, changing the time interval, could influence such gains on VO2max and aerobic performance. The aim of the study was to observe the possible influences of diferetes types of rest intervals in high intensity interval exercise protocol on VO2max, and the aerobic and anaerobic performances in 12 weeks of training.

Study Overview

Detailed Description

12-week experiment will be conducted, with a total of 30 high intensity interval training (HIIT) sessions in cycle ergometer. Both the first and the last week will serve to stabilize the basic values and also repeated after training. So, every other day will be held: 1) risk stratification for coronary artery disease, anthropometric measurements, cardiopulmonary test maximum effort; 2) stabilization of cardiopulmonary test values, determining the aerobic dependent variables: VO2max, peak power - PP, occurrence of power VO2max - PVO2Máx, maximum heart rate - HRMax, as well as familiarization with the HIIT protocol; 3) anaerobic performance test of 30 seconds determining the anaerobic dependent variables: peak lactate - LA, anaerobic power peak - PP, average power - PM. After the dependent variables have established, the subjects will be randomly distributed among three groups: two experimental and one control, and subjected to 30 sessions of HIIT (all out)with 30 seconds of stimulation in cycle ergometer, differentiated only by the recovery time (60 seconds and 120 seconds). The control group had only one continuous aerobic exercise (50-55% VO2max) with an average time similar to other training.

Study Type

Interventional

Enrollment (Anticipated)

36

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 Contact

  • Name: Sérgio E. Machado, PhD
  • Phone Number: 55 21 991567006
  • Email: secm80@gmail.com

Study Contact Backup

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 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • practitioners of aerobic activities for 6 mounths
  • negative prognosis for cardiovascular or metabolic disease

Exclusion Criteria:

  • muscle injuries
  • use ergogenic resources
  • cardiovascular disease
  • other limitations

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

  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: HIIT With 60 sec Rest
The experimental (1) group will be submitted at Six reps of 30 seconds of high intensity interval training (all out) with 60 seconds of interval rest for a total of 30 sessions of training. Dependents variables such as VO2Max and performance parameters are estimated before and after training sessions
30 sessions of High intensity interval training (all out) with 30 seconds of stimulous with 120 seconds rest on VO2Max and aerobic/ anaerobic performance
Other Names:
  • High intensity interval training with 120 seconds rest
Experimental: HIIT With 120 sec Rest
The experimental (2) group will be submitted at Six reps of 30 seconds of high intensity interval training (all out) with 120 seconds of interval rest for a total of 30 sessions of training. Dependents variables such as VO2Max and performance parameters are estimated before and after training sessions
30 sessions of High intensity interval training (all out) with 30 seconds of stimulous with 60 seconds rest on VO2Max and aerobic/ anaerobic performance
Other Names:
  • HIIT
  • High intensity interval training with 60 seconds rest
Active Comparator: Control
Continuous exercise at 50-55% of VO2max with similar total work
Continuous exercise at 50-55% VO2Max with similar total work of interval training
Other Names:
  • Control Continuous Exercise

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Oxygen Intake (VO2Max) Against of Differents Rest Time of High Intensity Interval Training
Time Frame: Change From Baseline VO2Max after 12 Weeks of High Intensity Interval Training
Change From Baseline VO2Max after 12 Weeks of High Intensity Interval Training

Secondary Outcome Measures

Outcome Measure
Time Frame
Aerobic and Anaerobic Power Peak Performance Against of Differents Rest Time of High Intensity
Time Frame: Change From Baseline in Aerobic and Anaerobic Performance after 12 Weeks of High Intensity Interval Training
Change From Baseline in Aerobic and Anaerobic Performance after 12 Weeks of High Intensity Interval Training
Lactate Concentration
Time Frame: Change From Baseline in Lactate Concentration after 12 Weeks of High Intensity Interval Training
Change From Baseline in Lactate Concentration after 12 Weeks of High Intensity Interval Training

Collaborators and Investigators

This is where you will find people and organizations involved with this 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

December 1, 2015

Primary Completion (Anticipated)

February 1, 2016

Study Completion (Anticipated)

April 1, 2016

Study Registration Dates

First Submitted

December 5, 2015

First Submitted That Met QC Criteria

December 25, 2015

First Posted (Estimate)

December 30, 2015

Study Record Updates

Last Update Posted (Estimate)

December 30, 2015

Last Update Submitted That Met QC Criteria

December 25, 2015

Last Verified

December 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • UNIVERSO-02

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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