The REACTIVE Trial

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: Between 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 09 Mar 2024. Study ID: 852291

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