Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05890274 · ClinicalTrials.gov registry record · NA

Atrial Fibrillation (AF) and Electrocardiogram (EKG) Interpretation Project ECHO

A NA study of Atrial Fibrillation, sponsored by University of North Carolina, Chapel Hill.

Active
Registry status
NA
Development phase
120
Enrollment target
3
Study locations

NCT05890274: Active NA study of Atrial Fibrillation, sponsored by University of North Carolina, Chapel Hill.

NCT05890274 is a NA study of Atrial Fibrillation that is active but no longer recruiting, run by University of North Carolina, Chapel Hill. The registered enrollment target is 120 participants, below the 2,996-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (96% lower). The trial reports 3 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05890274, a NA study of Atrial Fibrillation, is active but no longer recruiting, sponsored by University of North Carolina, Chapel Hill.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
120 participants
Enrollment target
3
Study locations

Study Summary

The goal of this study is to determine the effectiveness of a direct-to-provider virtual education program ("AF and EKG Interpretation Project ECHO") for primary care providers who manage patients with atrial fibrillation (AF). The main questions this study aims to answer are: 1. Will participants have improvement in knowledge and confidence in managing patients with atrial fibrillation after program completion? 2. Will quality and performance metrics improve at the patient level for program participants? Participants will be asked to: * Participate in 12 hours of virtual education sessions over twelve weeks via Zoom. * Complete a knowledge and confidence assessment online before the program starts and after its completion.

Primary Outcome

This outcome measures the number of patients prescribed appropriate anticoagulation medication based on risk factors for stroke including congestive heart failure (C), hypertension (H), Age \>74 (A2), Diabetes (D), prior stroke or transient ischemic attack (TIA) (S2), vascular disease (V), age 65-74 (A), female sex (Sc), commonly referred to as CHA2DS2-VASc stroke risk score for patients with atrial fibrillation. CHA2DS2-VASc score includes 7 indicators of stroke risk (age (\<65=0, 65-74=1, 75+=

Conditions Studied

Interventions

  • OTHER AF and EKG Interpretation Project ECHO

Study Locations (3)

North Carolina

  • University of North Carolina, Chapel Hill - Chapel Hill
  • Duke University - Durham
  • Wake Forest University - Winston-Salem

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2022-09-04
Est. Completion 2026-02
Phase NA

What the registry record for NCT05890274 still lists

NCT05890274 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 2,996-participant average among 202 other Atrial Fibrillation trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention - of which AF and EKG Interpretation Project ECHO is the first listed.

NCT05890274 reports a single indexed study location in North Carolina.

Frequently Asked Questions

What is clinical trial NCT05890274 about?

NCT05890274 is a clinical study titled "Atrial Fibrillation (AF) and Electrocardiogram (EKG) Interpretation Project ECHO". The goal of this study is to determine the effectiveness of a direct-to-provider virtual education program ("AF and EKG Interpretation Project ECHO") for primary care providers who manage patients with atrial fibrillation (AF). The main questions this study aims to answer are: 1. Will participants ...

What is the current status of trial NCT05890274?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2022-09-04. Estimated completion is 2026-02.

What conditions does trial NCT05890274 study?

This clinical trial studies the following conditions: Atrial Fibrillation.

What interventions are being tested in trial NCT05890274?

The interventions under investigation include: AF and EKG Interpretation Project ECHO (OTHER).

Who is sponsoring clinical trial NCT05890274?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05890274 being conducted?

This trial has 3 study locations across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Atrial Fibrillation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05890274's enrollment target sits among peer trials

120 131st of 202 higher than 69 of 202 other Atrial Fibrillation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Atrial Fibrillation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01174108 · 120 participants · Phase 2

    Allogeneic Hematopoietic Stem Cell Transplantation for Severe Aplastic Anemia and Other Bone Marrow Failure Syndromes Using G-CSF Mobilized CD34+ Selected Hematopoietic Precursor Cells Co-Infused With a Reduced Dose of Non-Mobilized Donor T-cells

  • NCT01627301 · 120 participants · NA

    Sympathetic Overactivity in Post-traumatic Stress Disorder

  • NCT02025023 · 120 participants · Phase 3

    Local 5-Fluorouracil Injection for the Treatment of Chalazia: A Prospective, Comparative Study

  • NCT02128906 · 120 participants · Phase 2

    Radiotherapy With Cisplatin vs. Docetaxel-cetuximab in HNSCC: ERCC1 Biomarker Enrichment and Interaction Design

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05890274, the US trial registry maintained by the National Library of Medicine. NCT05890274 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.