Actively Recruiting
The Effect of Menstrual Cycle Phase and Oral Contraceptive Use on Muscle Protein Metabolism Post-Resistance Training
Led by University of Toronto · Updated on 2025-12-02
20
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating how menstrual cycle phases and the use of oral contraceptives affect muscle protein synthesis after resistance exercise in females aged 18 to 40 years. This study aims to improve understanding of protein metabolism influenced by female sex hormones such as estrogen and progesterone, which have often led to exclusion of females in past research due to assumed variability. The findings will help develop better training and nutrition advice tailored for females. Participants will be randomly assigned to one of four groups representing different menstrual or contraceptive phases: mid-luteal phase, early follicular phase, active pill phase, or placebo pill phase. They will consume protein beverages enriched with stable isotope tracers ([D5]phenylalanine and [13C]phenylalanine) over an 8-hour period to measure muscle and whole-body protein synthesis. The study includes resistance exercise sessions and precise timing related to menstrual or contraceptive cycles. During the trial, participants will undergo tests including muscle protein synthesis measurement over 8 hours and whole-body protein synthesis over 4 hours. Researchers will monitor progesterone levels and dietary intake and evaluate the effects of resistance training combined with protein consumption. The study includes safety checks and assessments related to hormonal status, with participation lasting throughout the assigned menstrual or contraceptive phase timing.
CONDITIONS
Brief Title
Menstrual Cycle vs. Oral Contraceptives: Effects on Muscle Protein Metabolism After Resistance Exercise
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female aged 18 to 40 years
- Body mass index between 18.5 and 29.9 kg/m2
- Recreationally active, resistance training at least twice weekly
- Using monophasic or triphasic oral contraceptives for more than 1 year (oral contraceptive users)
- Regular menstrual cycles (21-35 days) for past 3 months and no hormonal contraceptive use for at least 6 months (non-oral contraceptive users)
- Meet progesterone sufficiency test (non-oral contraceptive users)
You will not qualify if you...
- Mid-luteal progesterone levels below 16 umol
- Diagnosed chronic diseases such as cardiovascular, thyroid, or diabetes
- Current or recent remission of cancer
- Regular use of NSAIDs (non-steroidal anti-inflammatory drugs) except low-dose aspirin, or anticoagulants
- Use of prescription drugs affecting muscle protein synthesis (e.g., statins, lithium, ADHD medication)
- Use of intrauterine device (IUD), except copper IUD
- Use of emergency contraception in the last 3 months
- Severe food allergies such as soy or nuts
- Smoking or use of performance-enhancing drugs like growth hormones or testosterone
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Each intervention phase lasts several days based on menstrual or pill cycle timing
Participants will consume protein beverages enriched with stable isotope tracers during different phases of the menstrual cycle or oral contraceptive use to assess muscle protein metabolism after resistance exercise.
Several visits scheduled according to menstrual and pill cycle phases
Trial Site Locations
Total: 1 location
1
Goldring Center for High Performance Sport
Toronto, Ontario, Canada, M5S 2C9
Actively Recruiting
Research Team
D
Daniel R Moore, PhD
I
Ines Kortebi, PhD Candidate
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
4
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