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Clinical Trials in Czechia / NCT07462286
Starting soon Observational

Menstrual Cycle and Women's Performance

NCT07462286 · tracked via the Priya Life Science Czechia tracker
Phase
Observational
Started
2026-04-01
Last updated
2026-03-10

Condition(s) studied

Menstrual CyclePhysical PerformanceMuscle StrengthMusculoskeletal SystemHealthy Volunteers

Investigational drug(s) / intervention(s)

Menstrual Cycle TrackingPerformance and Strength TestingMusculoskeletal AssessmentBody Composition and Symptom Assessment

Menstrual Cycle Tracking: Menstrual cycle monitoring using a mobile application for approximately 2 months to schedule laboratory visits to predefined cycle phases.

Performance and Strength Testing: Repeated lower-limb performance/strength assessments during laboratory visits in different menstrual cycle phases.

Musculoskeletal Assessment: Non-invasive assessment of selected muscle and tendon mechanical properties across cycle phases.

Body Composition and Symptom Assessment: Body composition measurement and collection of self-reported menstrual-related symptoms at laboratory visits.

Study summary

This study examines how different phases of the menstrual cycle are associated with selected performance and musculoskeletal parameters in physically active women aged 18-35 years.

Participants will track their menstrual cycle using a mobile app for approximately 2 months and attend 3 laboratory visits scheduled to specific cycle phases.

At each visit, participants will complete non-invasive assessments including lower-limb strength/performance testing, musculoskeletal measurements (muscle and tendon properties), body composition assessment, and symptom-related questionnaires.

The goal is to improve understanding of physiological variability across the menstrual cycle and support evidence-based planning of training, testing, and clinical practice in women.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Female, age 18-35 years Premenopausal Occasional to recreational level of physical activity Willing and able to track menstrual cycle using a mobile application for approximately 2 months Willing and able to attend 3 laboratory visits scheduled to predefined menstrual cycle phases Able to provide written informed consent Exclusion Criteria: * Irregular menstrual cycle (outside protocol-defined regularity) Current pregnancy Use of hormonal medication for therapeutic purposes (per protocol) Current acute illness at time of testing Musculoskeletal injury of the lower limb limiting safe performance testing Contraindication to body composition assessment methods used in the study (e.g., BIA/DXA, per site protocol) Any other condition that, in the investigator's judgment, may interfere with safe participation or data quality

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Physical Education and Sport, Charles University, José Martího 269/31 Prague Prague

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07462286 on ClinicalTrials.gov ↗ ← All trials in Czechia