Sprint Snacks: The Effects of Prolonged Rest on Reduced Exertion Interval Training.

Sponsor
University of British Columbia (Other)
Overall Status
Completed
CT.gov ID
NCT03159949
Collaborator
(none)
33
1
2
5.1
6.5

Study Details

Study Description

Brief Summary

An adapted sprint interval training protocol involving 2-3 repeated 20-second sprints separated by 2-3 minutes rest (termed reduced exertion high- intensity interval training (REHIIT)) has been developed and has been shown to promote fitness benefits. This data shows how little exercise one may need to improve cardiorespiratory fitness, provided they are willing to work very hard. However, it is unknown whether the benefits of REHIIT are because of the "all-out" nature of the sprint efforts themselves or the pattern of completing sprints with relatively short (i.e., minutes) rest periods within a workout session.

We are inquiring whether performing the same number and style of sprints with prolonged rest (i.e., 1-4 hours of rest in between sprints) is equally effective for improving aerobic fitness when compared to more traditional sprint interval training with 2-3 minutes of rest between sprints. Such information may make the effectiveness of sprint training more accessible and approachable for individuals unwilling or unable to plan a purposeful REHIIT exercise session into their day. If the rest interval could be prolonged then it may be possible to perform a few sprints as "exercise snacks" throughout the day without the need for a structured interval training session.

Condition or Disease Intervention/Treatment Phase
  • Other: REHIIT
  • Other: PR-REHIIT
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Masking Description:
Participants will know what exercise group they are assigned to.
Primary Purpose:
Prevention
Official Title:
Exercise Sprint Snacks: The Effects of Prolonged Rest, Reduced Exertion High-intensity Interval Training (PR-REHIIT) Compared to Standard Reduced Exertion High-intensity Interval Training (REHIIT).
Actual Study Start Date :
May 30, 2017
Actual Primary Completion Date :
Nov 1, 2017
Actual Study Completion Date :
Nov 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: PR- REHIIT

PR-REHIIT participants ("Sprint Snacks") will participate in 3 separate training session per day on 3 days per week (i.e., 9 sessions per week). Each session lasts 3 minutes and 20 seconds and consists of a two-minute warm-up, a 20-second "all-out" sprint, and a one-minute cool-down. There will be 1-4 hours of rest in between training sessions where participants are free to leave the lab and go about their normal day.

Other: PR-REHIIT
PR-REHIIT participants will come into the lab on 3 separate occasions on the training days, which occur 3 days per week (i.e., 9 sessions per week). Each session lasts 3 minutes and 20 seconds and consists of a two-minute warm-up, a 20-second "all-out" sprint on a cycle ergometer, and a one-minute cool-down. There will be 1-4 hours of rest in between training sessions where participants are free to leave the lab and go about their normal day.

Experimental: REHIIT

REHIIT participants will come into the lab one time per training days (3 training days per week), each session lasting 10 minutes. Training sessions involve a two-minute warm-up, 3 X 20-second sprints with three minutes rest in between, and a one-minute cool-down.

Other: REHIIT
REHIIT participants will come into the lab one time per training days (3 training days per week), each session lasting 10 minutes. Training sessions involve a two-minute warm-up, 3 X 20-second cycling sprints on an exercise bike with three minutes rest in between, and a one-minute cool-down.

Outcome Measures

Primary Outcome Measures

  1. Change in VO2max [Before and after the 6 week intervention]

    Maximal oxygen uptake assessed using a ramp increase protocol on a cycle ergometer.

Secondary Outcome Measures

  1. Change in 10 km Time Trial Performance [Before and after the 6 week intervention]

    Time to complete a simulated 10 km Time Trial on a Cycle ergometer

Other Outcome Measures

  1. Exercise Enjoyment Scale [6 weeks]

    This outcome will measure the enjoyment from either PR-REHIIT or REHIIT exercise intervention

  2. Intention Questionnaire [6 weeks]

    This outcome will measure the likelihood of an individual incorporating either PR-REHIIT or REHIIT into their exercise routine.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Physically inactive (2 or less bouts of purposeful exercise per week)
Exclusion Criteria:
  • If your doctor has informed you that you have a heart condition and should only do physical activity recommended by a doctor.

  • If you feel pain in your chest when you perform any physical activity.

  • If in the past the month you have had chest pain when you were not doing any physical activity.

  • If you lose your balance or consciousness because of dizziness.

  • If you have bone or joint problem (for example, back, knee, or hip) that could be made worse by a change in your physical activity.

  • If you are currently pregnant or planning on becoming pregnant in the next 6 weeks.

  • You have previously had a heart attack or stroke

  • You are currently engaging in high-intensity interval training.

  • You are currently physically active (engaging in 3 or more bouts of purposeful exercise per week; a "bout" is defined as structured, planned exercise lasting at least 30 minutes)

  • You have severe chest pain or blood pressure over 240/140 during baseline testing.

  • You have exercise induced asthma or a history of syncope.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of British Columbia Kelowna British Columbia Canada V1V 1V7

Sponsors and Collaborators

  • University of British Columbia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jonathan Little, Assistant Professor, University of British Columbia
ClinicalTrials.gov Identifier:
NCT03159949
Other Study ID Numbers:
  • H17-00641
First Posted:
May 19, 2017
Last Update Posted:
Nov 7, 2018
Last Verified:
Nov 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jonathan Little, Assistant Professor, University of British Columbia

Study Results

No Results Posted as of Nov 7, 2018