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NCT06142097 Clinical Trial

Sensor Technology Assessments of Reproductive Target Study

Menstrual Cycle Clinical Trial

— START  

Official title:
Sensor Technology Assessments of Reproductive Target Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06142097
Other study ID # OS22WH01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 15, 2022
Est. completion date April 2024

Study information
Verified date November 2023
Source Ouraring Inc.
Contact Clinical Study Coordinator
Phone 415-244-0913
Email startoura@ucsf.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this study was to better understand female reproductive health in the context of using wearable technology. Participants were provided and wore an Oura Ring, tracked their menstrual cycles, provided at-home ovulation test results, and had their cycles monitored via trans-vaginal ultrasounds. The study aimed to collect data from females with regular menstrual cycles.

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date April 2024
Est. primary completion date April 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 42 Years
Eligibility Inclusion Criteria: - Healthy women age 18-42 years - Regular menstrual cycles every 25-32 days - Own an iPhone or Android mobile device - Agree to follow study protocol such as wearing the Oura Ring for the duration of the study, at-home ovulation testing, present for frequent ultrasounds Exclusion Criteria: - Non-English speaking - Current use of hormonally active medications - History of infertility - History of recurrent pregnancy loss - Current circadian disruptions

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States UCSF Center for Reproductive Health San Francisco California

Sponsors (2)
Lead Sponsor Collaborator
Ouraring Inc. UCSF Center for Reproductive Health

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Retrospective ovulation day 6 months
Primary Prospective ovulation day 6 months
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