Heart Rate Variability During the Menstrual Cycle

Further Investigations of Heart Rate Variability During the Menstrual Cycle

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04382001

Enrollment

Registered

2020-05-11

Start date

2020-06-01

Completion date

2021-05-06

Last updated

2021-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovulation

Brief 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.

Detailed 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.

Interventions

None listed

Study design

Observational model

OTHER

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Inclusion criteria

* Aged 18 years of age and over * Regular menstrual cycles (23-35 days in length)-

Exclusion criteria

* Taking any hormonal medications * Taking any medications that may affect heart rate * Known heart condition or use of a pacemaker * Skin condition where there is sensitivity to wearing a skin monitor * Currently suffering with anxiety or panic attacks * Pregnant or breastfeeding * Undertaking any frequent travel or long-haul flights during the course of the study * Does not have access to an Apple iPhone or iPad with Bluetooth 4.0 (or later) and iOS 10.0 (or later)

Design outcomes

Primary

Measure	Time frame	Description
Heart rate	1 month	Heart rate at time points throughout the menstrual cycle
Heart Rate	1 month	Heart rate variability at time points throughout the menstrual cycle
Day of Ovulation	1 month	Day of ovulation determined by urinary LH surge +1 day
Fertile Window	1 month	Fertile window onset determined by E3G surge
Fertile window	1 month	Fertile window closure determined by P3G rise

Secondary

Measure	Time frame	Description
Comparisons between wrist and chest band monitors	1 month	Agreement between wrist band and chest band heart rate data

Countries

United Kingdom

Outcome results