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Effect of Sprint Interval Training Frequency on Improvements in Fitness

Effect of Sprint Interval Training Frequency on Cardiorespiratory Fitness Adaptations

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06142942
Enrollment
100
Registered
2023-11-22
Start date
2023-11-01
Completion date
2024-08-31
Last updated
2023-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiorespiratory Fitness

Keywords

sprint interval training, maximal oxygen consumption, training intervention

Brief 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.

Interventions

OTHERExercise Intervention

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

Sponsors

Wilfrid Laurier University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

All pre- and post-testing is completed by researchers not involved in training, and thus are blinded to which group participants are assigned to. This prevents any potential bias when researchers are completing post-testing sessions.

Intervention model description

Following pre-testing participants are assigned to one of the four groups based on their baseline cardiorespiratory fitness to ensure no differences between groups at baseline. Participants will train 2, 3, or 4 days a week, or be assigned to the control group (no training) and re-test following the 4 week intervention.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
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

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

Design outcomes

Primary

MeasureTime frameDescription
Cardiorespiratory fitnessThis 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

Secondary

MeasureTime frameDescription
Anaerobic performanceThis 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.

Countries

Canada

Contacts

Primary ContactTom J Hazell, PhD
thazell@wlu.ca5488893902

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026