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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03159949
Other study ID # H17-00641
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 30, 2017
Est. completion date November 1, 2017

Study information

Verified date November 2018
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date November 1, 2017
Est. primary completion date November 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

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.
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.

Locations

Country Name City State
Canada University of British Columbia Kelowna British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Exercise Enjoyment Scale This outcome will measure the enjoyment from either PR-REHIIT or REHIIT exercise intervention 6 weeks
Other Intention Questionnaire This outcome will measure the likelihood of an individual incorporating either PR-REHIIT or REHIIT into their exercise routine. 6 weeks
Primary Change in VO2max Maximal oxygen uptake assessed using a ramp increase protocol on a cycle ergometer. Before and after the 6 week intervention
Secondary Change in 10 km Time Trial Performance Time to complete a simulated 10 km Time Trial on a Cycle ergometer Before and after the 6 week intervention
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