Timing of Physician Rounds for Antepartum Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorDuke University

About this trial

This study will include patients admitted to the Antepartum service at Duke University Hospital, many of whom are managing high-risk pregnancies that require extended hospital stays and frequent physician interactions. Currently, two rounding methods are used interchangeably for patients who do not have pregnancy or delivery complications that would preclude participation in delayed daytime rounding. This randomized controlled trial will compare two rounding models: the standard model, in which patients receive two rounds (an early morning bedside encounter and a later team discussion), and the intervention model, which consolidates both rounds into a single, later-morning bedside encounter following the team's review of clinical data. The primary objective is to assess whether consolidating physician rounds into a single, later-morning encounter-referred to as discovery rounding-improves patient satisfaction with communication.

Eligibility criteria

Qualifiers

Pregnant women greater than 20 weeks gestation admitted to the antepartum list at Duke University Hospital

Disqualifiers

Stillbirth

ICU admission

Admission to off-service unit

Active magnesium sulfate administration

Trial design

Treatments tested in this trial

  • Discovery Rounding
  • Standard Rounding

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators