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Menstrual Cycle Phase and Oral Contraceptive Pill (OCP) Use on Muscle Protein Synthesis

Influence of Menstrual Cycle Phase and Oral Contraceptive Pill (OCP) Use on the Muscle Protein Synthetic Response to Exercise in Young, Healthy Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05347667
Enrollment
24
Registered
2022-04-26
Start date
2022-05-01
Completion date
2024-04-30
Last updated
2025-01-01

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

Conditions

Menstrual Cycle, Muscle Protein Synthesis, OCP, Resistance Exercise

Brief summary

Skeletal muscle size and function is regulated by various factors, including hormones. While we understand the role of male sex hormones (testosterone), we aren't sure how female sex hormones (estrogen and progesterone) influence muscle mass and strength. Female physiology is unique in that hormones fluctuate throughout the menstrual cycle. In the first phase (follicular phase) following menstruation, estrogen levels are high while progesterone levels are low. In the second phase (luteal phase), progesterone levels are high. Females are often excluded from studies because researchers are concerned that the menstrual cycle might affect the results. The purpose of this study is to investigate the response to resistance exercise in each phase of the menstrual cycle.

Interventions

One leg will perform unilateral resistance exercise

OTHERControl Leg

One leg will serve as a non-exercise control

Sponsors

Natural Science and Engineering Research Council of Canada (NSERC)
CollaboratorUNKNOWN
McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

In a randomized fashion, participants will have one leg undergo unilateral resistance exercise training to assess the muscle protein synthetic response in each menstrual cycle phase OR each pill phase (active vs. placebo)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy females, between the ages of 18 and 30 y with a regular menstrual cycle * Body Mass Index between 18.5 and 30.0 kg/m2 * Able and willing to provide informed consent

Exclusion criteria

* A history of neuromuscular disorders or muscle/bone wasting diseases * Any acute or chronic illness, cardiac, pulmonary, liver, or kidney abnormalities, uncontrolled hypertension, insulin-dependent or insulin-independent diabetes, or the presence of any other metabolic disease - all of which will be determined via a medical history screening questionnaire * The use of any medications known to affect protein metabolism (glucocorticoids, non-steroidal anti-inflammatory medication, or prescription strength acne medication, etc.) * A (family) history of thrombosis * The use of anticoagulant medications * Consumption of tobacco-containing products * Excessive alcohol consumption (\>21 units/wk) * History of bleeding diathesis, platelet or coagulation disorders * Currently pregnant * Irregular menstrual cycle as defined in the study protocol

Design outcomes

Primary

MeasureTime frameDescription
Change in Rates of Muscle Protein Synthesis6 daysThe investigators will use deuterated water and skeletal muscle biopsies to calculate the synthesis of skeletal muscle proteins.

Secondary

MeasureTime frameDescription
Whole-body proteolysis6 daysThe investigators will use 3-methylhistidine in urine to calculate the rate of whole-body myofibrillar protelysis

Countries

Canada

Outcome results

None listed

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