Clinical Trial

Timing of Physician Rounds for Antepartum Patients

Recruiting
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Summary
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.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-10-09; most recent amendment 2026-01-28.
Status change: Not Yet Recruiting → Recruiting 2025-11-03
Trial Details
NCT Number NCT07215507
Lead Sponsor Duke University
Conditions Physician Rounds, Communication
Enrollment 200 participants
Start Date 2025-11-04
Primary Completion 2027-01-30 (estimated)
Study Completion 2027-02-20 (estimated)
Updated on ClinicalTrials.gov 2026-01-29