Trials / Not Yet Recruiting
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
| Type | Name | Description |
|---|---|---|
| OTHER | Menstrual Cycle Tracking | Menstrual cycle monitoring using a mobile application for approximately 2 months to schedule laboratory visits to predefined cycle phases. |
| OTHER | Performance and Strength Testing | Repeated lower-limb performance/strength assessments during laboratory visits in different menstrual cycle phases. |
| OTHER | Musculoskeletal Assessment | Non-invasive assessment of selected muscle and tendon mechanical properties across cycle phases. |
| OTHER | Body Composition and Symptom Assessment | Body 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.