Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
NCT06647511

Digital Solutions to Reduce Maternal Morbidity and Mortality in Pregnant Refugee Women

Led by Weill Medical College of Cornell University · Updated on 2026-04-22

75

Participants Needed

1

Research Sites

207 weeks

Total Duration

On this page

Sponsors

W

Weill Medical College of Cornell University

Lead Sponsor

N

National Academy of Medicine

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Digital Solutions to Reduce Maternal Morbidity and Mortality in Pregnant Refugee Women

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Weill Cornell Medicine

New York, New York, United States, 10065

Actively Recruiting

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Research Team

G

Gunisha Kaur, MA, MD

CONTACT

M

Michele Steinkamp, RN

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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