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

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:

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.

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

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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