Image

Influence of Menstrual Cycle Phase on Adaptations to Sprint Interval Training

Influence of Menstrual Cycle Phase on Adaptations to Sprint Interval Training

Recruiting
18-35 years
Female
Phase N/A

Powered by AI

Overview

Sprint interval training improves endurance performance and induces metabolic adaptations in muscle. Most research demonstrating these responses has been conducted in males, with limited studies evaluating changes to endurance performance and skeletal muscle oxidative capacity in females. Moreover, it is currently unknown if training in specific phases of the menstrual cycle influences adaptations to training. Thus, the purpose of the present study is to compare adaptations to 2 weeks of sprint interval training performed in the follicular vs. luteal phase of the menstrual cycle in healthy, eumenorrheic women.

Description

The primary purpose of the present study is to determine if menstrual cycle phase influences adaptations to 2 weeks of sprint interval training. Participants will be randomized to perform 6 sessions of sprint interval training over 2 weeks in either the Follicular Phase or Luteal Phase of their individual menstrual cycle. Blood and urine sampling will be used to confirm menstrual cycle phases. Training will involve 4-6 x 30-second Wingate sprints with 4 minutes of rest in between (~14-28 min per session). Before and after the training intervention, investigators will measure participant's aerobic and anaerobic performance, cardiorespiratory fitness and skeletal muscle outcomes. Performance and fitness measures are performed on on a stationary bike, and muscle outcomes are measured by taking a small amount of muscle from the vastus lateralis (thigh) muscle.

This study will advance knowledge on how the menstrual cycle influences adaptations to training in females

Eligibility

Inclusion Criteria:

  • Participating in 150 min of moderate-vigorous physical activity/week
  • VO2peak of 'good' or above based on American College of Sport Medicine (ACSM) normative values(greater than 35.0ml/kg/min)
  • Body mass index (BMI) between 18-27 kg/m2
  • Performing 2-4 structured exercise sessions/week.
  • Weight stable (within ± 2kg for at least 6 months)
  • Non-smoker
  • Menstrual cycle length of 27-35 days
  • Minimal menstrual cycle length variability (less than 3 days)
  • Ovulating monthly evidenced by a positive urinary luteinizing hormone surge
  • Blood progesterone concentration greater than 16 nmol/L.

Exclusion Criteria:

  • Hormonal contraceptive use within the last 3 months
  • Polycystic ovarian syndrome (PCOS) or endometriosis
  • Failure to meet MC verification criteria.
  • Diagnosed with cardiovascular or metabolic disease, hyper- or hypogonadism, and/or PCOS
  • The use of medication for managing blood glucose or lipid metabolism
  • Current use of oral contraceptives or use within the last 3 months
  • Irregular menstrual cycles (<27 days or >35 days)
  • Pregnant or post-partum in the last 12 months, lactating or breast feeding within 3 months of the start of study, or menopausal
  • Recreational smoking tobacco
  • Inability to perform the study exercise protocols or follow the pre-trial dietary or physical activity controls
  • Taking medications affecting substrate metabolism (corticosteroids or nSAIDs)
  • Actively engaging in a low-carbohydrate diet (e.g., ketogenic, Atkins)

Study details
    Healthy

NCT06744517

University of Toronto

10 September 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.