Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
ID06647511

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

N/A

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

This research aims to improve the detection of high blood pressure and related pregnancy health issues in pregnant refugee women using digital health tracking. The study focuses on testing and refining a digital monitoring system to identify gestational hypertension and associated risks like preeclampsia. The goal is to enhance diagnosis accuracy compared to clinical standards, ultimately supporting targeted treatment for this population. Participants will use digital devices such as smartwatches and electronic blood pressure monitors to collect health data at home over 24 months. They will record weekly blood pressure readings with devices like the Nokia-Withings BPM Connect, entering data into a smartphone app. Continuous tracking via Apple Watches and Fitbit Versa 3 will monitor heart rate, activity, and sleep. The study includes baseline and follow-up in-person visits with surveys to assess health, stress, and related risks. Throughout the study, participants will complete questionnaires, regular blood pressure checks, pain and trauma assessments, and clinical monitoring. Researchers will evaluate the digital system's ability to detect gestational hypertension with high sensitivity and track comorbid conditions. They will also assess referrals to healthcare providers and retention of participant contact. The main outcome is the system's digital sensitivity in detecting hypertension, monitored over a maximum 13-month enrollment period.

CONDITIONS

Brief 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
  • 18 years of age or older
  • Has a personal smartphone
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Considered in an extremely vulnerable position by the principal investigator and not suited for research participation
  • Plans to move from the New York City 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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 13 months

Participants are monitored through digital health tracking with devices to collect cardiovascular and health data, as well as complete questionnaires and assessments.

Weekly visits for blood pressure measurements and ongoing passive data collection via smartwatches

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

M

Michele Steinkamp, RN

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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