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Heart Rate Variability During the Menstrual Cycle

NCT04382001 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 28

Last updated 2021-08-06

No results posted yet for this study

Summary

In this study, women will be required to wear a chest heart rate monitor and wrist heart rate monitor daily and collect daily early morning urine samples for the duration of one complete menstrual cycle. This will enable comparisons between data collected from the heart rate monitor and hormone analysis in urine samples to be made.

Conditions

  • Ovulation

Sponsors & Collaborators

  • SPD Development Company Limited

    lead INDUSTRY

Principal Investigators

  • Sarah Johnson · SPD Development Company

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-01
Primary Completion
2021-05-06
Completion
2021-05-06

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04382001 on ClinicalTrials.gov