Transforming ED Throughput With AI-Driven Clinical Decision Support System (TEDAI)

July 28, 2023 updated by: National Taiwan University Hospital

Transforming ED Throughput With AI-Driven Clinical Decision Support System (TEDAI): The Impact on the Delivery of Care and Patient Experience

The aims of this study is to integrate real-time data flow infrastructure between hospital information system and AI models and to conduct a cluster randomized crossover trial to evaluate the efficacy of the AI models in improving patient flow and relieving ED crowding.

Study Overview

Study Type

Interventional

Enrollment (Actual)

4016

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan
        • National Taiwan University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • ED patients aged 20 years or older
  • Patients were treated by the recruited 16 ED attendings.

Exclusion Criteria:

  • Patients aged less than 20 years.
  • Patients were not treated by the recruited 16 ED attendings.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: AI-assisted
AI-assisted models providing diagnosis and prognostic information
AI-assisted models providing diagnosis and prognostic information in the ED, including triage, ICD coding, chest x ray alerts, critical event alerts, readmission prediction, and post-cardiac arrest prognostication.
Placebo Comparator: Usual care
usual care without AI-assisted models providing diagnosis and prognostic information
Critical treatment of the emergency room

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
ED length of stay
Time Frame: From ED arrival to 3 days after ED discharge. For hospitalized patients with cardiac arrest, the outcome ascertainment continues until hospital discharge.
From ED arrival to 3 days after ED discharge. For hospitalized patients with cardiac arrest, the outcome ascertainment continues until hospital discharge.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Dr. Huang, National Taiwan University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 30, 2022

Primary Completion (Actual)

December 31, 2022

Study Completion (Actual)

April 27, 2023

Study Registration Dates

First Submitted

February 28, 2022

First Submitted That Met QC Criteria

February 28, 2022

First Posted (Actual)

March 9, 2022

Study Record Updates

Last Update Posted (Actual)

August 1, 2023

Last Update Submitted That Met QC Criteria

July 28, 2023

Last Verified

July 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 202108090RINC

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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