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RECRUITING
NCT06647511

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

Sponsor: Weill Medical College of Cornell University

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

75

Start Date

2024-09-12

Completion Date

2026-09

Last Updated

2025-05-18

Healthy Volunteers

Yes

Interventions

DEVICE

Nokia-Withings BPM Connect Blood Pressure Monitor

At-home blood pressure (BP) measurements will be weekly via a blood pressure cuff (e.g., Nokia-Withings BPM (Beats per Minute) Connect), with measurements being manually entered into the study specific smartphone app.

DEVICE

Smartwatch Devices

Passive continuous collection of digital data (e.g., daily heart rate trends, activity levels, sleep measurements) for exploratory outcomes will occur via Apple Watches and Fitbit Versa 3s, which are synced to a smartphone application.

Locations (1)

Weill Cornell Medicine

New York, New York, United States