The REACTIVE Trial
Not Recruiting
18 years - 50 years
Female
Phase
N/A
400 participants needed
2 Locations
Brief description of study
The goal of this clinical trial is to determine the effectiveness of remote nonstress test (NST) compared to in-clinic NSTs in improving fetal testing completion rates. Participants will be randomized to either in-clinic NSTs or use of an FDA-approved remote monitoring belt for their pregnancy monitoring.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Pregnant,Fetal monitoring,Nonstress test
-
Age: 18 years - 50 years
-
Gender: Female
Inclusion Criteria:
- Singleton pregnancy
- Gestational age between 30 weeks 0 days and 35 weeks 6 days
- Pregnant patients who have clinical indication for fetal surveillance with NSTs (based on UPHS Health System clinical guidelines for antenatal monitoring)
- Able to provide written consent
- English speaking
Updated on
27 May 2025.
Study ID: 22-1331
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