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RecruitingNCT06142942Updated Nov 27, 2023

Effect of Sprint Interval Training Frequency on Improvements in Fitness

An interventional study of Exercise Intervention in Cardiorespiratory Fitness, sponsored by Wilfrid Laurier University. Recruiting at 1 site in Canada. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-11-27.

Sponsored by Wilfrid Laurier University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Aug 2024, 2 years 2 months ago, but the record still lists the study as recruiting.
  • Started Nov 2023; still recruiting 2 years 11 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Non-randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Cardiorespiratory Fitness

Keywords

  • sprint interval training
  • maximal oxygen consumption
  • training intervention
03

In context

Lead sponsor

Wilfrid Laurier University is the lead sponsor of 15 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

Exclusion Criteria:

  • Smoking
  • Consuming supplements known to affect metabolism (e.g., creatine, carnitine, nitric oxide, brain chain amino acids).
  • Failure to meet inclusion criteria
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    2 days per week group

    Participants in this group complete 2 training sessions each week (Monday and Thursday).

    Other: Exercise Intervention

  • Experimental
    3 days per week group

    Participants in this group complete 3 training sessions each week (Monday, Wednesday, and Friday).

    Other: Exercise Intervention

  • Experimental
    4 days per week group

    Participants in this group complete 4 training sessions each week (Monday, Tuesday, Thursday, and Friday).

    Other: Exercise Intervention

  • No intervention
    No-exercise Control group

    This group does not complete any training intervention. They are asked to maintain their regular physical activity habits.

Interventions

  • OtherExercise Intervention

    Participants will complete an exercise intervention where they will exercise 2, 3, or 4 days per week for 4 weeks.

06

What researchers measure

Primary outcomes

  1. Cardiorespiratory fitness

    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

    Time frame: This will be assessed before and after 4 weeks of training (or control).

Secondary outcomes

  1. Anaerobic performance

    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.

    Time frame: This will be assessed before and after 4 weeks of training (or control).

07

Study locations

1 of 1 sites recruiting
  • Wilfrid Laurier University
    Waterloo, Ontario N2L 3C5, Canada
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — Data will be made available to other researchers upon reasonable request.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 27, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06142942
Lead sponsor
Wilfrid Laurier University
Responsible party
Tom Hazell (Principal Investigator, Wilfrid Laurier University) — Principal investigator
First posted
Nov 22, 2023
Start date
Nov 1, 2023
Primary completion
Aug 2024 (estimated)
Completion
Aug 2024 (estimated)
Last update
Nov 27, 2023

Study contacts

Tom J Hazell, PhD
Contact
thazell@wlu.ca
5488893902
Tom J Hazell, PhD
principal investigator · Wilfrid Laurier University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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