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Not Yet RecruitingNCT07462286

Menstrual Cycle and Women's Performance

The Relationship Between the Menstrual Cycle and Physical Performance in Women

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
32 (estimated)
Sponsor
Charles University, Czech Republic · Academic / Other
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Accepted

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.

Detailed description

Background and rationale: Female physiology changes across menstrual cycle phases, which may influence neuromuscular performance, perceived symptoms, and selected tissue/mechanical properties. Current evidence is heterogeneous, partly due to methodological differences in cycle-phase identification and measurement protocols. This study aims to provide standardized data from repeated within-subject assessments across the menstrual cycle. Objectives: Primary objective is to evaluate associations between menstrual cycle phase and selected performance-related outcomes in physically active women. Secondary objectives are to explore phase-related differences in musculoskeletal parameters, body composition outputs, and self-reported symptoms. Study design: Prospective, repeated-measures observational study. Each participant is measured repeatedly across predefined menstrual cycle phases. Participants: Women from the general population, 18-35 years, with occasional to recreational physical activity level. Procedures: Screening and eligibility confirmation according to protocol criteria. Menstrual cycle tracking via mobile application for approximately 2 months. Three laboratory visits timed to predefined cycle phases. At each visit, non-invasive assessments are performed, including: lower-limb strength/performance testing, assessment of muscle and tendon mechanical properties, body composition measurement, recording of subjectively perceived menstrual-related symptoms. Outcomes: Main outcomes include phase-specific differences/associations in selected performance and musculoskeletal variables; additional outcomes include symptom profiles and selected body-composition variables. Duration and setting: Individual participation lasts approximately 2 months including cycle tracking and 3 lab visits (approximately 60-90 minutes per visit). Study procedures are conducted at FTVS UK (Prague). Ethics and data protection: Participation is voluntary, and participants may withdraw at any time without giving a reason. Data are processed in compliance with applicable data-protection regulations (including GDPR), pseudonymized for analysis, and reported in aggregate/anonymized form. The study is conducted according to institutional ethics approval and the Declaration of Helsinki.

Conditions

Interventions

TypeNameDescription
OTHERMenstrual Cycle TrackingMenstrual cycle monitoring using a mobile application for approximately 2 months to schedule laboratory visits to predefined cycle phases.
OTHERPerformance and Strength TestingRepeated lower-limb performance/strength assessments during laboratory visits in different menstrual cycle phases.
OTHERMusculoskeletal AssessmentNon-invasive assessment of selected muscle and tendon mechanical properties across cycle phases.
OTHERBody Composition and Symptom AssessmentBody composition measurement and collection of self-reported menstrual-related symptoms at laboratory visits.

Timeline

Start date
2026-04-01
Primary completion
2026-09-30
Completion
2027-03-30
First posted
2026-03-10
Last updated
2026-03-10

Locations

1 site across 1 country: Czechia

Source: ClinicalTrials.gov record NCT07462286. Inclusion in this directory is not an endorsement.