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Cardiac point-of Care Ultrasound Training Pathway for Emergency Department Advanced Practice Providers

Cardiac Point-of-care Ultrasound Clinical Training Pathway Implementation and Impact Assessment for Advanced Practice Providers in the Emergency Department

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07159269
Enrollment
75
Registered
2025-09-08
Start date
2025-11-13
Completion date
2030-06-30
Last updated
2026-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Tamponade, Cardiovascular Disease Acute, Diagnostic Imaging, Emergency Department Patient, Heart Failure Acute, Implementation Science, Medical Training, Pericardial Effusion, Point of Care Ultrasound (POCUS), Pulmonary Embolism (Diagnosis)

Keywords

point of care ultrasound, focused cardiac ultrasound, advanced practice provider training, medical education, implementation science

Brief summary

The aim of this study is to assess emergency medicine physician and advanced practice provider (APP) knowledge and technical skill in performance of a point-of-care ultrasound simulation and just-in-time training pathway to determine the feasibility, acceptability, and usability of the ultrasound training program. By performing this study, we hope to create a standardized training model which could potentially facilitate point-of-care ultrasound (POCUS) clinical performance and thereby improve patient care.

Interventions

BEHAVIORALCardiac point-of-care ultrasound (POCUS) training and clinical pathway

Participants will complete a cardiac POCUS simulation session and a hands-on observed structured clinical skill exam (OSCE) post-training led by ultrasound-trained faculty. Then as part of standard clinical care, advanced practice providers (APPs) will perform POCUS while supervised by emergency medicine (EM) attending physicians. To assess program feasibility and acceptability, participants will complete a pre/post and 6-month post-survey and semi-structured interview, as well as a knowledge and technical skills assessment.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

prospective cohort study

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* advanced practice providers (APPs) currently working in our ED, with additional APPs as they are hired (expected to be about 75 APPs total within the next 3 years due to expanding staffing needs and coverage models).

Exclusion criteria

* non-APPs such as physicians, nurses, or other clinical staff

Design outcomes

Primary

MeasureTime frameDescription
Aim 1: Assess the feasibility of implementing a just-in-time cardiac point-of-care ultrasound (POCUS) clinical training pathway for advanced practice providers (APPs) using the Reach Effectiveness Adoption Implementation Maintenance (RE-AIM) framework.1-2 years for each study siteParticipants will complete a cardiac POCUS simulation session and a hands-on structured clinical skill exam post-training (OSCE) led by ultrasound-trained faculty. Then as part of standard clinical care, APPs will perform POCUS while supervised by EM attending physicians. The primary outcome assesses program feasibility and acceptability. Participants will complete a pre/post and 6-month post-survey and semi-structured interview. Survey questions are structured based on the Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM), and Feasibility of Intervention Measure (FIM) survey tool. This is scored on a Likert scale from 1-5.
Aim 1: Acceptability of the Intervention as measured by the Acceptability of Intervention Measure (AIM)1-2 years for each study siteThe AIM is scored on a Likert scale from 1 to 5, where a higher score indicates greater acceptability.
Aim 1: Appropriateness of the Intervention as measured by the Intervention Appropriateness Measure (IAM)1-2 years for each study siteThe IAM is scored on a Likert scale from 1 to 5, where a higher score indicates greater appropriateness.
Aim 1: Feasibility of the Intervention as measured by the Feasibility of Intervention Measure (FIM) survey tool1-2 years for each study siteThe FIM is scored on a Likert scale from 1 to 5, where a higher score indicates greater appropriateness.

Secondary

MeasureTime frameDescription
Aim 1: Feasibility of implementing a just-in-time cardiac point-of-care ultrasound (POCUS) clinical training pathway for advanced practice providers (APPs) using the Reach Effectiveness Adoption Implementation Maintenance (RE-AIM) framework.1-2 years for each study siteUsing a modified framework analysis approach, a team of 3-4 trained research assistants and the two emergency ultrasound fellows led by an implementation science expert will deductively analyze semi-structured interview content based on RE-AIM constructs with open inductive coding for data that does not fit into the framework. The investigators will perform a preliminary rapid qualitative deductive analysis based on audio recordings and meeting notes applied to the RE-AIM dimensions, to determine scope and saturation. Coding and categorization will be conducted with RE-AIM templated coding sheets and transferred to NVivo.
Aim 2: Educational impact of the training model on point-of-care ultrasound (POCUS) use and diagnostic performance1-2 years for each study siteParticipants will complete a pre-, post-, and 6-month post-training knowledge assessment and technical skill test to assess the educational impact of the cardiac POCUS program, structured using the Ultrasound Competency Assessment Tool (UCAT), which is scored on a Likert scale from 1-5, where a higher score indicates greater competency.
Aim 2: Clinical impact of the training model on point-of-care ultrasound (POCUS) use and diagnostic performance - number of clinical POCUSs performed1-2 years for each study siteTo assess the advanced practice provider (APP) training program effectiveness, the investigators will collect pre/post-health record data on the number of clinical POCUS performed in the emergency department pre/post-intervention (from the Butterfly ultrasound archiving system, units in counts/percentages).
Aim 2: Clinical impact of the training model on point-of-care ultrasound (POCUS) use and diagnostic performance - image quality1-2 years for each study siteTo assess APP training program effectiveness, the investigators will collect pre/post-health record data on image quality review scores (determine by two ultrasound experts, Likert scale 1-5, where a higher score indicates greater quality).
Aim 2: Clinical impact of the training model on point-of-care ultrasound (POCUS) use and diagnostic performance - diagnostic accuracy1-2 years for each study siteThe investigators will collect data on diagnostic accuracy as compared to radiology studies (from ultrasound expert review, True Positive, True Negative, False Positive, False Negative, or Technically-limited study)
Aim 2: Clinical impact of the training model on point-of-care ultrasound (POCUS) use and diagnostic performance - time to initial cardiology consult1-2 years for each study siteThe investigators will collect electronic health record data on pre/post-intervention time to initial cardiology consult (both from the Epic electronic health record, units in hours).
Aim 2: Clinical impact of the training model on point-of-care ultrasound (POCUS) use and diagnostic performance - emergency department length-of-stay1-2 years for each study siteThe investigators will collect electronic health record data on pre/post-intervention ED length-of-stay (from the Epic electronic health record, units in hours).
Aim 2: Impact of the training model on cost-effectiveness1-2 years for each study siteThe investigators will collect pre/post-intervention POCUS revenue data for cost-effectiveness (from hospital billing data, units in dollars).

Countries

United States

Contacts

CONTACTRebecca G Theophanous, MD, MHSc
rebecca.theophanous@duke.edu919-681-0196
CONTACTAbha Singh
abha.singh@duke.edu919-668-8700
PRINCIPAL_INVESTIGATORRebecca G Theophanous, MD, MHSc

Duke University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026