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Investigation of Heart Rate Variability During the Menstrual Cycle

Investigation of Heart Rate Variability During the Menstrual Cycle

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04008277
Enrollment
12
Registered
2019-07-05
Start date
2019-07-19
Completion date
2019-12-31
Last updated
2020-02-20

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 heart rate monitor continuously 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 pilot 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 heart rate monitor continuously and collect daily early morning urine samples throughout one menstrual cycle. 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 monitor including heart rate and heart rate variability will be downloaded for comparison.

Interventions

None listed

Sponsors

SPD Development Company Limited
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 18 years and over * Regular menstrual cycles

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

Design outcomes

Primary

MeasureTime frameDescription
Heart Rate1 monthHeart rate at time points throughout the menstrual cycle
Heart Rate Variability1 monthHeart rate variability at time points throughout the menstrual cycle

Secondary

MeasureTime frameDescription
Day of ovulation1 monthDay of ovulation determined by urinary LH surge +1 day
Fertile window1 monthFertile window onset determined by E3G surge
Fertile window closure1 monthFertile window closure determined by P3G rise

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026