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Not listed No phase listed Observational

Clinical Decision Support for Atrial Fibrillation and Flutter

ClinicalTrials.gov ID: NCT05009225

Public ClinicalTrials.gov record NCT05009225. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 9:26 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Reducing Variation in Hospitalization and Processes of Care in Emergency Department Patients With Atrial Fibrillation: A Stepped Wedge Cluster Randomized Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Atrial fibrillation (AF) is a major public health problem: it impairs quality of life and independently heightens the risks of ischemic stroke, heart failure and all-cause mortality. AF is a common reason for presenting to emergency departments (ED) in Kaiser Permanente Northern California (KPNC) and is associated with frequent hospitalization. Additionally, inter-facility hospitalization rates for AF vary across KPNC. Improvements in modifiable components of ED AF care could potentially reduce low-yield hospitalizations and the associated costs, patient inconveniences, and complications that can ensue. Real-time clinical decision support systems (CDSS) can transform entrenched physician practices and improve patient outcomes. The investigators will conduct a stepped-wedge cluster randomized trial of a CDSS intervention across 13 KPNC EDs for the comprehensive management of acute AF with the following three aims: 1) To evaluate the impact of the CDSS intervention on index hospitalization rates; 2) To evaluate the impact of the CDSS intervention on ED AF rate and rhythm control process-of-care metrics; and 3) To evaluate the impact of the CDSS intervention on AF stroke prevention actions for eligible participants at the time of ED discharge. The investigators hypothesize that the CDSS intervention will safely reduce index hospitalization rates, improve rate and rhythm control process-of-care metrics, and increase stroke prevention actions for eligible participants at ED discharge and within 30 days.

Study identification

NCT ID
NCT05009225
Recruitment status
Not listed
Study type
Observational
Phase
Not listed
Lead sponsor
Kaiser Permanente
Other
Enrollment
4,000 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2021
Primary completion
Apr 29, 2023
Completion
Jun 29, 2024
Last update posted
Mar 5, 2024

2021 – 2024

United States locations

U.S. sites
16
U.S. states
1
U.S. cities
15
Facility City State ZIP Site status
Kaiser Permanente Antioch Emergency Department Antioch California 94531
Kaiser Permanente Fremont Emergency Department Fremont California 94538
Kaiser Permanente Manteca Medical Center Manteca California 95337
Kaiser Permanente Modesto Medical Center Modesto California 95356
Kaiser Permanente Oakland Emergency Department Oakland California 94611
Kaiser Permanente Richmond Emergency Department Richmond California 94801
Kaiser Permanente Roseville Emergency Department Roseville California 95661
Kaiser Permanente South Sacramento Emergency Department Sacramento California 95823
Kaiser Permanente Sacramento Emergency Department Sacramento California 95825
Kaiser Permanente San Francisco Emergency Department San Francisco California 94115
Kaiser Permanente San Jose Emergency Department San Jose California 95119
Kaiser Permanente San Leandro Emergency Department San Leandro California 94577
Kaiser Permanente San Rafael Emergency Department San Rafael California 94903
Kaiser Permanente Santa Clara Emergency Department Santa Clara California 95051
Kaiser Permanente South San Francisco Emergency Department South San Francisco California 94080
Kaiser Permanente Walnut Creek Medical Center Walnut Creek California 94596

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05009225, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 5, 2024 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05009225 live on ClinicalTrials.gov.

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