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NCT Number: NCT06744517

Influence of Menstrual Cycle Phase on Adaptations to Sprint Interval Training

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.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Goldring Centre for High Performance Sport

Toronto, Ontario, M5S 2C9, Canada

Location status: Recruiting

Location contact

Jenna Gillen

CONTACT

[email protected]

4169783244

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Sprint Interval Training

Other

6 sessions of sprint interval training over 2 weeks. Each session involves 4-6 x 30 second Wingate sprints with 4 minutes of recovery in between on a stationary bike

Primary outcomes

  1. Endurance performance

    Time frame: Before and after 2 weeks of exercise training

    Time to completion and average power output during a 250kJ time trial

Secondary outcomes

  1. Skeletal muscle mitochondrial content

    Time frame: Before and after 2 weeks of exercise training

    Measured via Western blotting

  2. Skeletal muscle mitochondrial enzyme activity

    Time frame: Before and after 2 weeks of exercise training

    Measured via enzyme activity assays

  3. Skeletal muscle capillarization

    Time frame: Before and after 2 weeks of exercise training

    Measured via immunofluorescence

  4. Skeletal muscle lipid content

    Time frame: Before and after 2 weeks of exercise training

    Measured via immunofluorescence

  5. Skeletal muscle protein synthesis

    Time frame: Before and after 2 weeks of exercise training

    Measured via the incorporation of a stable isotope tracer during the 2 weeks of training

  6. Cardiorespiratory fitness

    Time frame: Before and after 2 weeks of exercise training

    Measured via a maximal exercise test on a cycle ergometer

  7. Anaerobic exercise performance

    Time frame: Before and after 2 weeks of exercise training

    Power output during a Wingate anaerobic test

Study contacts

Contact information is provided by the study sponsor or research team.

Jenna Gillen Assistant Professor, PhD

CONTACT

[email protected]

4169783244

Sponsors and collaborators

Lead sponsor

University of Toronto

Other

Registry information

Official study title

Influence of Menstrual Cycle Phase on Metabolic and Performance Adaptations to Sprint Interval Training

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 20, 2024
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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