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Emergency Department Re-evaluation Software Pilot Study

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Duke University

Status

Completed

Conditions

Emergency Department Waiting Room Congestion

Treatments

Other: ED management software

Study type

Interventional

Funder types

Other

Identifiers

NCT05831046
PRO00113113

Details and patient eligibility

About

This is a research study to determine a method in improving emergency department waiting room care by using new software program.

Full description

This is a pilot study to determine the effectiveness of an emergency department re-evaluation software, to improve patient flow through an emergency department. The end goal of the study is to provide proof of the efficacy of the software and provide data such that the software can be improved upon. The study will include ED waiting room patients. The study will involve interaction with the software on a tablet for patients and software on a desktop for providers. The providers utilizing the software will not be considered part of the study, but rather focusing on the outcomes of the patients using the software. Patients will be selected by the provider as available for re-evaluation. Each patient will then be randomized into either a control group (software not used) and a "study" group (software used). Data analysis will be performed in conjunction with clinical statisticians at our institution. The risks of this study are primarily derived from patient privacy concerns, which have been addressed in the risk section.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

  • Individuals that are 18 and older who have been identified with completed lab work.
  • Their primary language must be English to follow the instructions of the study.
  • Cognitively sound

Exclusion:

  • Minors
  • Emergency Severity Index (ESI) class 1 patients
  • Individual who cannot legally give consent
  • Pregnant patients
  • Non-english speakers

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

20 participants in 2 patient groups

Study Arm
Experimental group
Description:
Patients who undergo use of the software prior to being re-evaluated by a physician
Treatment:
Other: ED management software
Healthy Control
No Intervention group
Description:
Patients undergo care without using the software

Trial contacts and locations

1

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Central trial contact

Mitchell Veverka, MD

Data sourced from clinicaltrials.gov

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