Build status - In Progress

The REACTIVE Trial

The REACTIVE Trial
Recruiting
16 years - 55 years
Female
Phase N/A
400 participants needed
1 Location

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: 16 years - 55 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 04 Aug 2024. Study ID: 852291

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