Actively Recruiting
Remote Fetal Monitoring in High Risk Pregnancies
Led by Beth Israel Deaconess Medical Center · Updated on 2026-03-09
50
Participants Needed
1
Research Sites
87 weeks
Total Duration
On this page
Sponsors
B
Beth Israel Deaconess Medical Center
Lead Sponsor
B
Biorithm Pte Ltd
Collaborating Sponsor
AI-Summary
What this Trial Is About
Antenatal nonstress tests (NSTs) are performed to assess fetal health and are used as a cost-effective test that can be widely administered. However, an NST is operator-dependent due to the nature of Doppler ultrasound and is primarily performed in a clinic and hospital setting. The ability to conduct a clinically valuable test at home would address access to care issues faced by numerous women in the United States and reduce the workload on healthcare clinicians facing a shortage of human resources. This pilot study aims to assess the feasibility and acceptability of home NST monitoring in order to determine whether femomTM could be utilized as an adjunct to routine prenatal care. Patients with high risk pregnancies who are recommended to undergo at least once weekly at 32 weeks testing by the obstetrician will be recruited for participation in this study. Participants will be asked to perform three 30 minute monitoring sessions weekly starting at 32 weeks for 6 weeks.
CONDITIONS
Official Title
Remote Fetal Monitoring in High Risk Pregnancies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Intrauterine pregnancy greater than 32 weeks gestation
- Recommended for at least once weekly antenatal fetal testing by their obstetrician
- English-speaking
You will not qualify if you...
- Under age 18 years of old
- Non-english speaking
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02115
Actively Recruiting
Research Team
E
Ethan Litman, MD, MS
CONTACT
C
Chloe Zera, MD, MPH
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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