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Study identifier: NCT06647511 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Gestational Hypertension  ·  Sponsor: Weill Medical College of Cornell University

PhaseN/A
Planned participants75
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Gunisha Kaur, MA, MD  ·  (212) 746-2461  ·  gus2004@med.cornell.edu

Michele Steinkamp, RN  ·  2127462953  ·  mls9004@med.cornell.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Weill Cornell MedicineNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06647511