About this trial
The investigators will obtain urine hormone results and validated menstrual bleeding score from people experiencing abnormal uterine bleeding. The investigators will evaluate satisfaction and ease of use of Mira monitor. The investigators will measure recruitment rate, attrition and cycle collection completeness of data. The investigators will evaluate menstrual health literacy at baseline and at the conclusion of the study.
Eligibility criteria
Qualifiers
35 years and older
Have experienced AUB
Disqualifiers
Currently pregnant or become pregnant during their participation
Previous surgeries impairing the menstrual cycle (e.g. hysterectomy, bilateral oophorectomy)
Currently or in the previous 3 months on medications that are known to impair or stimulate ovulation (e.g. oral contraceptives, ovulation stimulants, hormone replacement, etc.)
Trial design
Treatments tested in this trial
- Not listed