About this trial
The goal of this observational study is to use digital health tracking to improve how high blood pressure and other health issues are detected in pregnant refugee women. The main questions this study aims to answer are are:
* Can a digital monitoring system that checks for high blood pressure in these women be tested and refined, using clinical training and validation? * Can this digital monitoring system accurately track any related pregnancy health issues and be used to refer participants to care providers? * Can this system be used to accurately identify risks associated with the contraction of pregnancy-related conditions, such as preeclampsia and high blood pressure?
Participants will:
* Complete baseline and follow-up in-person appointments; * Complete surveys at these appointment that track their health, stress levels, and comorbidities/risks associated with pregnancy; * Be given a smartwatch fitness tracker and electronic blood pressure cuffs for at-home measurements.
Eligibility criteria
Qualifiers
Pregnant
Refugee, asylum seeking, or asylee as designated by the U.S. Government
Greater than or equal to 18 years of age
Has a personal smartphone
Disqualifiers
Unable to provide informed consent
Determined by the PI to be in an extremely vulnerable position and therefore not suited for research participation
Planned move from the New York City (NYC) area within the next 24 months
Trial design
Treatments tested in this trial
- Nokia-Withings BPM Connect Blood Pressure Monitor
- Smartwatch Devices
Treatment groups
Sponsors and collaborators
Weill Medical College of Cornell University
Lead sponsor
National Academy of Medicine
Collaborator
Cornell University
Collaborator
Apple Inc.
Collaborator