Heart Rate Variability During the Menstrual Cycle

Status Completed

Clinical Trial 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.

Clinical Trial Description

This study is a prospective observational study of women's heart rate and heart rate variability throughout one complete menstrual cycle. A minimum of 10 volunteers aged 18 years of age or over will be recruited via a variety of methods according to the criteria detailed in section 9. They will be required to wear a chest heart rate monitor and wrist heart rate monitor for 1 hour each day, and throughout the night for one menstrual cycle. In addition, a daily early morning urine sample will be collected throughout the study. Urine samples will be returned to SPD on a regular basis for measurement of urinary hormones related to pregnancy and fertility. Data collected via the monitors including heart rate and heart rate variability will be downloaded for comparison. ;

Study Design

Related Conditions & MeSH terms

Ovulation

Clinical Trial Details

NCT number	NCT04382001
Study type	Observational
Source	SPD Development Company Limited
Contact
Status	Completed
Phase
Start date	June 1, 2020
Completion date	May 6, 2021

View Details

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