- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06142942
Effect of Sprint Interval Training Frequency on Improvements in Fitness
November 21, 2023 updated by: Tom Hazell, Wilfrid Laurier University
Effect of Sprint Interval Training Frequency on Cardiorespiratory Fitness Adaptations
The goal of this study is to learn how the number of weekly exercise sessions affects improvements in fitness in healthy university aged students.
The main question it aims to answer is how training frequency affects improvements in fitness.
Participants will complete a pre-testing sessions to assess fitness level and sprint performance.
Following this participants are assigned to one of four groups.
A group that exercises 2 days a week, a group that trains 3 days a week, a group that trains 4 days a week, or a no-exercise control group.
Participants in this group will not complete any training and allow the researchers to compare the exercise groups to a group that didn't train.
Each participant will train for 4 weeks.
During each training session participants will complete 4-6 30 second all-out sprints with 4 minutes of rest between each.
Participants will complete the same tests they did during the pre-testing session following the 4 weeks of training to see how frequency affects improvements.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
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: Tom J Hazell, PhD
- Phone Number: 5488893902
- Email: thazell@wlu.ca
Study Locations
-
-
Ontario
-
Waterloo, Ontario, Canada, N2L 3C5
- Recruiting
- Wilfrid Laurier University
-
Contact:
- Tom J Hazell, PhD
- Phone Number: 548-889-3902
- Email: thazell@wlu.ca
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Recreationally active: exercising at least 2-3 days per week and not currently involved in, or had been involved in a systematic training program for at least 3 months prior to data collection.
- Safe to become physically active based on the Canadian Society for Exercise Physiology - Get Active Questionnaire.
Exclusion Criteria:
- Smoking
- Consuming supplements known to affect metabolism (e.g., creatine, carnitine, nitric oxide, brain chain amino acids).
- Failure to meet inclusion criteria
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 2 days per week group
Participants in this group complete 2 training sessions each week (Monday and Thursday).
|
Participants will complete an exercise intervention where they will exercise 2, 3, or 4 days per week for 4 weeks.
|
|
Experimental: 3 days per week group
Participants in this group complete 3 training sessions each week (Monday, Wednesday, and Friday).
|
Participants will complete an exercise intervention where they will exercise 2, 3, or 4 days per week for 4 weeks.
|
|
Experimental: 4 days per week group
Participants in this group complete 4 training sessions each week (Monday, Tuesday, Thursday, and Friday).
|
Participants will complete an exercise intervention where they will exercise 2, 3, or 4 days per week for 4 weeks.
|
|
No Intervention: No-exercise Control group
This group does not complete any training intervention.
They are asked to maintain their regular physical activity habits.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cardiorespiratory fitness
Time Frame: This will be assessed before and after 4 weeks of training (or control).
|
Cardiorespiratory fitness will be assessed through the measurement of maximal oxygen consumption.
This will be determined using an incremental exercise test to volitional fatigue on a treadmill.
A metabolic cart will be used to assess oxygen consumption using indirect calorimetry
|
This will be assessed before and after 4 weeks of training (or control).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anaerobic performance
Time Frame: This will be assessed before and after 4 weeks of training (or control).
|
Anaerobic performance will be assessed during one 30 second "all-out" sprint completed on a self-propelled treadmill.
Participants will be instructed to run as fast and as hard as they can for the entire 30 seconds.
Speed will be recorded during this sprint and used to determine, peak, average, and minimum speed, as well as fatigue index.
|
This will be assessed before and after 4 weeks of training (or control).
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tom J Hazell, PhD, Wilfrid Laurier University
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)
November 1, 2023
Primary Completion (Estimated)
August 1, 2024
Study Completion (Estimated)
August 1, 2024
Study Registration Dates
First Submitted
November 15, 2023
First Submitted That Met QC Criteria
November 15, 2023
First Posted (Actual)
November 22, 2023
Study Record Updates
Last Update Posted (Actual)
November 27, 2023
Last Update Submitted That Met QC Criteria
November 21, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- EMRL-23-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Data will be made available to other researchers upon reasonable request.
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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