Can your smartwatch help you navigate menopause?
NCT ID NCT07597915
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to learn more about the menopause journey by collecting data from wearable devices and a smartphone app. Researchers will track symptoms and daily experiences in 1,250 women aged 35-55 to help both individuals and doctors better understand perimenopause and menopause. The goal is to empower women to manage this transition by identifying what helps or worsens their symptoms.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 1,250 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Eligible participants will live in the US or Canada. Up to 250 participants will be invited to participate in the main cohort, 75 in the hormone sub-cohort, and 70 in the Vire clip sub-cohort.
- Ages
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35 to 55 years
- Sex
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Female participants only
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Are 35-55 years old * Reside in the US or Canada * Are able to speak, write, and read English * Are able to provide informed consent * Have a personally owned iPhone (iOS Version 16.4) Exclusion Criteria: * Are not willing to wear a wearable study device * Have a hormonal intrauterine device (IUD) * Are taking birth control pills * Are taking systemic estrogen or progesterone * Have been diagnosed with Polycystic ovary syndrome (PCOS) * Are taking the following medications (cancer treatment that affects the menstrual cycle, thyroid medication) * Have had the following procedures (hysterectomy \[removal of uterus\], bilateral, oophorectomy \[removal of both ovaries\], endometrial ablation \[surgery that destroys the lining of the uterus\]) * Are currently pregnant, attempting to conceive, recently pregnant and not yet cycling and currently breast feeding
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As listed by the trial registrant
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How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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