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Our Transitions: Improving the Path to Menopause With Personal Digital Health Technologies

Our Transitions: Improving the Path to Menopause With Personal Digital Health Technologies

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07597915
Enrollment
1250
Registered
2026-05-20
Start date
2026-05-01
Completion date
2027-08-31
Last updated
2026-05-20

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

Conditions

Menopause, Perimenopause

Keywords

Perimenopause, Menopause, Menopause Transition, Wearables, Oura, Fitbit

Brief summary

The goal of this observational study is to build knowledge about the path to menopause using subjective, self-reported and objectively measured information from multiple wearable study devices and a smartphone app. This study is being done in female individuals who are 35-55 years of age. The eventual aim of this work is two-fold; 1) to increase knowledge, awareness and education for individuals and clinicians about the lived experience of perimenopause and menopause through objectively measured data from digital study devices, and 2) to develop approaches to empower female individuals to manage this transition by learning what improves or worsens their symptoms.

Detailed description

The ultimate objective of this research is to determine the feasibility of using multiple wearable study devices and smartphone apps to detect, track and learn how to share insights about symptoms during the path to menopause. The investigators anticipate that up to 250 participants will participate for 6 to 9 months. Participants will complete surveys and active tasks in a study app that takes on average 5 minutes a day, be provided with an Oura Ring Gen 4 and a Fitbit Sense 2 and will be expected to wear them daily. Participants will be expected to check in with a research coordinator every two weeks to go over participations and provide feedback on the wearable devices and smartphone apps. A subset of participants will be invited to participate in an at-home daily urine hormone collection for 3 menstrual cycles, measuring hormones including Luteinizing Hormone (LH), Estrone-3-glucuronide (E3G), and Pregnanediol Glucuronide (PdG). A different subset will be invited to participate in a vasomotor detection cohort using the new Vire Clip that captures core body temperature through heat flow, the dynamics of respiratory effort, and skin conductance measures at multiple layers of the skin. There will be a 'Bring Your Own Device' cohort after the main cohort enrollment is complete, where those with a personal wearable device will be invited to participate in the use of the study app for 6 to 9 months. Investigators will collect self-reported subjective symptoms and objectively measured physiological information to understand what participants learn about the use of these tools in tracking peri/menopausal symptoms. This study is done in collaboration between 4YouandMe, Women Living Better, Vector Institute, and is funded by the Steven and Alexandra Cohen Foundation.

Interventions

None listed

Sponsors

4YouandMe
Lead SponsorOTHER
Steven & Alexandra Cohen Foundation
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 55 Years

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

Design outcomes

Primary

MeasureTime frameDescription
Feasibility: RetentionFrom enrollment to the end of participation at 12 monthsProportion of participants retained according to study protocol
Feasibility: AdherenceFrom enrollment to the end of participation at 12 monthsMean adherence to completing in-app daily study measures

Contacts

CONTACTSarah Goodday, PhD
sarah@4youandme.org902-237-4235

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 21, 2026