- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06329427
Dragon Ambient eXperience (DAX) Copilot Evaluation (DAX)
March 27, 2024 updated by: Wake Forest University Health Sciences
Dragon Ambient eXperience (DAX) Express Pilot Evaluation
AI solutions like, Dragon Ambient eXperience (DAX) Copilot (Nuance/Microsoft), hold the potential to significantly enhance provider and patient interactions and alleviate pain points that contribute to burn out.
Atrium Health was the first healthcare system in the world to pilot Nuance's DAX Copilot intelligence (AI) enabled scribe software, which synthesizes a draft clinic note by "listening" to the conversation between a provider and patient.
After 180 days of use by primary care clinicians and advanced practice providers (APPs), along with a control group, the investigators assess provider satisfaction, patient experience, and provider efficiency through qualitative and quantitative methods.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In this non-randomized stepped-wedge trial, clinicians (including physicians and advanced practice providers [APP]) specializing in family medicine, internal medicine, and general pediatrics were recruited from outpatient clinics located in North Carolina and Georgia.
The intervention group was divided into 5 waves between June and August 2023 based on clinic locations.
Prior to the activation of accounts, clinicians underwent a one-hour training session on DAX Copilot.
Meanwhile, a comparison group comprising clinicians not utilizing DAX was recruited in five waves from locations and specialties similar to those of the intervention group.
Two types of primary outcomes, electronic health record (EHR) metrics and financial metrics, were assessed after 180 days of intervention.
EHR metrics include time in EHR (EHR8), work time outside of work (WOW8), time in documentation (Note8), completed appointment rate, same day closure rate, and note length.
Financial metrics include gross revenue per visit and work relative value units (wRVU) per visit.
Secondary outcome include provider satisfaction survey, provider interview, and patient satisfaction survey.
Study Type
Interventional
Enrollment (Actual)
238
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
-
-
Georgia
-
Macon, Georgia, United States, 31201
- Atrium Health Navicent
-
Rome, Georgia, United States, 30165
- Atrium Health Floyd
-
-
North Carolina
-
Charlotte, North Carolina, United States, 28203
- Atrium Health
-
Laurinburg, North Carolina, United States, 28352
- Scotland Health Care System
-
Winston-Salem, North Carolina, United States, 27157
- Atrium Health Wake Forest Baptist
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- clinicians specializing in family medicine, internal medicine, and general pediatrics (including physicians and advanced practice providers [APPs])
- (intervention group) showed interests in participating in Dragon Ambient eXperience (DAX) Copilot
- (control group) clinicians who opted out from Dragon Ambient eXperience (DAX) Copilot in vendor's baseline survey
- (control group) clinicians who worked in the same clinic/region as the intervention group
Exclusion Criteria:
- preceptors
- inactive DAX participants (i.e., had DAX license but never activate it)
- have the same first use and last use DAX date
- missing demographics
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: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Intervention - Dragon Ambient eXperience (DAX)
Clinicians interacted with DAX Copilot
|
The tool (DAX) listens to the conversation between a clinician and patient/caregiver during their visit, provides transcriptions between different speakers for the clinician to review, edit, and included in the final EHR notes.
Other Names:
|
|
No Intervention: No Intervention - Control group
Clinicians with standard care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total EHR time
Time Frame: Month 10
|
Total time on EHR (during and outside of clinic sessions) per 8 hour of patient scheduled time.
|
Month 10
|
|
Work outside of work
Time Frame: Month 10
|
Time on EHR outside of scheduled patient hours per 8 hour of patient scheduled time.
|
Month 10
|
|
Time on encounter note documentation
Time Frame: Month 10
|
Hours on documentation (note writing) per 8 hour of scheduled patient time
|
Month 10
|
|
Completed appointment rate
Time Frame: Month 10
|
Total completed visits over scheduled visits
|
Month 10
|
|
Same day closure rate
Time Frame: Month 10
|
Number of visits closed on the same day over total scheduled visits
|
Month 10
|
|
Note length
Time Frame: Month 10
|
Length of note in EPIC for each visit
|
Month 10
|
|
Gross revenue per visit
Time Frame: Month 10
|
Total charged amount in each day over total completed visits on the same day
|
Month 10
|
|
wRVU per visit
Time Frame: Month 10
|
Total work relative value units (wRVU) in each day over total completed visits on the same day
|
Month 10
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Provider satisfaction
Time Frame: Month 4
|
REDCap survey to clinicians in both groups (intervention and control) and assess their satisfaction of the new tool.
|
Month 4
|
|
Provider interview
Time Frame: Month 1
|
12 semi-structured interview on clinicians in the intervention group.
Each interview was facilitated using an interview guide with a semi-structured list of questions to help guide the conversation and answer the learning objectives.
|
Month 1
|
|
Patient satisfaction
Time Frame: Month 6
|
Patient satisfaction on the visit - patient satisfaction surveys are collected as part of routine care, which will be accessed through Medallia.
Scores range between 0 (worst) to 10 (best) with one decimal point.
|
Month 6
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Tsai-Ling Liu, PhD, Wake Forest University Health Sciences
- Principal Investigator: Timothy C Hetherington, MS, Wake Forest University Health Sciences
- Study Chair: Jeffrey A. Cleveland, MD, FAAP, Wake Forest University Health Sciences
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)
June 19, 2023
Primary Completion (Actual)
December 15, 2023
Study Completion (Actual)
December 15, 2023
Study Registration Dates
First Submitted
March 18, 2024
First Submitted That Met QC Criteria
March 22, 2024
First Posted (Actual)
March 26, 2024
Study Record Updates
Last Update Posted (Actual)
March 29, 2024
Last Update Submitted That Met QC Criteria
March 27, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- IRB00098063
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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