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Quantum Natural Family Planning Pilot

Comparison of Two Hormonal Fertility Monitors for Use in Natural Family Planning

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03908697
Acronym
QNFP
Enrollment
26
Registered
2019-04-09
Start date
2020-05-29
Completion date
2021-04-22
Last updated
2025-03-24

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

Conditions

Fertility Disorders

Brief summary

•The Pilot study will involve current Marquette Method users who own and use a ClearBlue Fertility monitor and who will be asked to simultaneously use the Mira monitor for the sake of comparing the two devices to monitor the menstrual cycle.

Detailed description

* The Mira fertility monitoring system (www.miracare.com) is a new home-use hormone tracking device with the ability to quantitatively measure reproductive hormones in the urine but is also synced to a smart phone App that provides a graphic representation of the hormonal levels throughout a menstrual cycle. * The Mira monitor will be compared to the ClearBlue Fertility Monitor for its ease of use, satisfaction, and accuracy. * The Mira hormonal monitor and App system has not been tested for its use in Natural Family Planning (NFP). * The Pilot study will involve current Marquette Method users who own and use a ClearBlue Fertility monitor and who will be asked to simultaneously use the Mira monitor for the sake of comparing the two devices. * Female participants invited to participate will need to meet the following criteria: * Age 18 to 42 years * Menstrual cycle ranging between 21-42 days * At least 3 cycles after cessation of breastfeeding * Not currently on medications that affect ovulation and 3 months prior * Not currently pregnant or breastfeeding * No known fertility problems * Not planning on achieving pregnancy during the 3 menstrual cycles of the study

Interventions

DEVICEMira monitor comparison to ClearBlue monitor

Testing first morning urine with hormone test sticks at home

Sponsors

Quanovate Tech Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Masking description

Anonymized demographic data

Intervention model description

Prospective cohort analysis of three menstrual cycles of hormone data, comparing two fertility monitors that analyze urine hormones. Satisfaction and ease of use will be assessed using surveys. Individual data will be anonymized.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 42 Years
Healthy volunteers
Yes

Inclusion criteria

* • Menstrual cycle ranging between 21-42 days * At least 3 cycles after cessation of breastfeeding

Exclusion criteria

* • Not currently on medications that affect ovulation and 3 months prior * Not currently pregnant or breastfeeding * No known fertility problems * Not planning on achieving pregnancy during the 3 menstrual cycles of the study

Design outcomes

Primary

MeasureTime frameDescription
Day of the estimated beginning of the fertile phase of the menstrual cycle:3 monthsFirst day of the estimated fertile phase as measured by Clearblue Fertility Monitor First day of the estimated fertile phase as measured by the MIRA Fertility Monitor
Day of the estimated peak of the fertile phase of the menstrual cycle:3 monthsPeak day of the estimated fertile phase as measured by the Clearblue Fertility Monitor Peak day of the estimated fertile phase as measured by the MIRA Fertility Monitor
Day of the estimated end of the fertile phase of the menstrual cycle:3 monthsLast day of the estimated fertile phase as measured by the Clearblue Fertility Monitor Last day of the estimated fertile phase as measured by the MIRA Fertility Monitor

Secondary

MeasureTime frameDescription
Satisfaction and Ease of Use of a Electronic Fertility Monitor:3 monthsMeasured by the modified 8 item Severy Satisfaction Scale Total score rages from 8 - 24 with 24 being the highest satisfaction

Countries

Canada

Outcome results

None listed

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