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Computer Interpretation of the ECG Raising Awareness CIERA Trial (CIERA)

14 maggio 2026 aggiornato da: Amer Ali Hasanien, University of Jordan

The Effect of Three Educational Interventions on Emergency and Critical Nurses Proficiency in Computer Interpretation of the ECG: Results of the CIERA Trial

Background: Practice guidelines require emergency and critical care nurses (ECC) to be skillful in ECG and cardiac monitoring. Evidence suggests that nurses' proficiency is still inadequate with this regard. Computer interpretation of the ECG (CIE) is accurate and improves clinicians' accuracy in ECG interpretation. Unfortunately, nurses are not taught or trained to use this technology. Through this study the investigators aim to evaluate the effectiveness of three educational interventions to improve ECC nurses' proficiency in CIE.

Methods. The investigators applied a randomized mixed, crossover and parallel, design. Linear mixed model analysis was used to examine differences in CIE test score among groups and across time. There were three interventional groups (G0, no intervention then flyer; G1, face-to-face then online; and G2, online then face-to-face) with three points of time measurement (T0, baselines; T1, after first intervention, and T2 after second intervention).

Panoramica dello studio

Descrizione dettagliata

Nurses working in the emergency department and critical care units spend a great deal of their time reading or recording ECGs. Practice guidelines require nurses working in units where cardiac monitoring is essential to be skillful in electrocardiography and cardiac monitoring. However, evidence suggests that nurses are still far from achieving this goal. In a study conducted in 65 cardiac care units from three different countries, nurses' (n, 3013) mean total score on an online ECG test was below 50%. However, nurses' mean total score significantly improved after receiving an online ECG monitoring education program. In another study published recently, emergency department and critical care nurses' (n, 210) mean total score in an ECG proficiency test was 18.1 out of 34 with only 61.9% of nurses scoring equal to or higher than 50% of the maximum score. Inadequate nurses' performance on ECG interpretation and cardiac monitoring skills can delay or even prevent lifesaving treatment.

One way of improving emergency and critical care nurses' (ECC) ECG interpretation accuracy is through the utilization of the computer interpretation of the ECG (CIE). This tool is incredibly accurate for certain interpretation algorithms to an extent comparable to a cardiologist, which is considered the gold standard for ECG interpretation. The CIE overall accuracy is estimated to be 90 to 93%. CIE combined with an "over-read" by a well-trained interpreter represents the most accurate form currently available for ECG interpretation. Existing evidence supports CIE ability to improve health care professionals' interpretation accuracy. In a recent study, CIE improved nurses' interpretation accuracy by 16.2%, improved cardiology fellows accuracy by 10.9% , resident physicians by 14.4%, and medical students by 19.9%. In the same study, CIE increased interpretation confidence by 0.06 on a scale from 0 to 1 for all study participants.

In addition to accuracy and improving clinicians' interpretation, especially for less experienced readers, CIE has several other advantages. CIE is especially useful when access to an interpretation expert is not possible; it minimizes expenses; does not fatigue; does not become distracted by outside pressure; objective; not affected by intra or inter-observer variability; decreases interpretation time, on average, by 52 seconds and by 24-28% for the experience reader; makes interpretation easier because it requires no deep knowledge; can take into account age, gender, race, and medication therapy; capable of doing automated serial ECG comparisons; capable of applying multiple and complex criteria, for example in diagnosing left ventricular hypertrophy, that would be difficult or impossible to apply otherwise; leads to faster diagnoses and earlier treatment; can unify diagnostic statements terminology through the following of the terminology adopted by practice guidelines. Such unification of terminology in electrocardiography would facilitate better patient care and unify teaching curriculum all over the world. CIE also continues to improve over time especially with AI evolving technology.

CIE has also several limitations. CIE is generally inaccurate in diagnosing arrhythmia, conduction disturbances, and pace maker rhythms. It is also inaccurate in diagnosing ischemia and myocardial infarction. It is inaccurate in measuring the QT interval, diagnosing long QT interval, and measuring QRS duration. It is inaccurate in diagnosing atrial fibrillation. It misdiagnoses atrial fibrillation and atrial flutter. It does not identify left and right arm lead reversal. The wide variability among different interpretation software with regard to accuracy and employed measurement criteria is another major limitation. However, even with these limitations, the CIE is still considered overall to be accurate.

Nevertheless, despite its great usefulness and potential to advance nursing practice and patient's care, unfortunately nurses are not taught or trained to use this technology. Formal undergraduate, graduate, and clinical education and textbooks do not talk about CIE. Even in research studies evaluating nurses' knowledge and proficiency in electrocardiography, researchers do not include testing items concerning CIE. As far as the investigators know, there is no previous study that has ever specifically evaluated nurses' knowledge in CIE.

The investigators aim from this project which we call "Computer Interpretation of the ECG Raising Awareness CIERA" to raise awareness among nurse practitioners, educators, and managers about the utilization of this technology. Specifically, the investigators aim to introduce three educational interventions (face-to-face, online, and flyer) and assess their effectiveness in improving ECC nurses' proficiency in computer interpretation of the ECG.

The investigators followed the "CONSORT 2010 statement: extension to randomized crossover trials" guidelines in reporting the findings of this trial.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

268

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Amman, Giordania, 11942
        • The University of Jordan

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Every nurse working in the emergency department and critical care units of the participating hospitals

Exclusion Criteria:

  • None

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Altro
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: no intervention then a flyer
the flyer was a small, palm-sized, crafted from fine-quality material, thoughtfully designed to be colorful, visually inviting, and easy going, featuring carefully selected introductory images, ample whitespace, and minimal text to ensure clarity, quick engagement, and polished first impression.
the flyer was a small, palm-sized, crafted from fine-quality material, thoughtfully designed to be colorful, visually inviting, and easy going, featuring carefully selected introductory images, ample whitespace, and minimal text to ensure clarity, quick engagement, and polished first impression.
Sperimentale: Face-to-face then online lectures
the face-to-face content included audiovisual aids, case scenarios, and immediate feedback discussions. The online content included artificial intelligence enhanced audiovisual aids (videos and images), integrated interactive feedback mechanisms (e.g., requiring the participant to scan a QR code and respond to real-time MCQ questions). The face-to-face lecture time was totally 45 minutes. The online total lecture time was 25 minutes.
the face-to-face content included audiovisual aids, case scenarios, and immediate feedback discussions. The face-to-face lecture time was totally 45 minutes
The online content included artificial intelligence enhanced audiovisual aids (videos and images), integrated interactive feedback mechanisms (e.g., requiring the participant to scan a QR code and respond to real-time MCQ questions). The online total lecture time was 25 minutes.
Sperimentale: Online then face-to-face lectures
the face-to-face content included audiovisual aids, case scenarios, and immediate feedback discussions. The online content included artificial intelligence enhanced audiovisual aids (videos and images), integrated interactive feedback mechanisms (e.g., requiring the participant to scan a QR code and respond to real-time MCQ questions). The face-to-face lecture time was totally 45 minutes. The online total lecture time was 25 minutes.
the face-to-face content included audiovisual aids, case scenarios, and immediate feedback discussions. The face-to-face lecture time was totally 45 minutes
The online content included artificial intelligence enhanced audiovisual aids (videos and images), integrated interactive feedback mechanisms (e.g., requiring the participant to scan a QR code and respond to real-time MCQ questions). The online total lecture time was 25 minutes.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Emergency and Critical Care Nurses Proficiency in Computer Interpretation of the ECG
Lasso di tempo: From enrollment to the end of treatment at 5 months
Emergency and Critical Care Nurses scores on the "Computer Interpretation of the ECG" test score. The test is scored out of 28 (range 0 to 28), with higher scores indicating greater proficiency. The test scale name is "Computer Interpretation of the ECG" test scale
From enrollment to the end of treatment at 5 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Amer M Hasanien, PhD, The University of Jordan

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 febbraio 2025

Completamento primario (Effettivo)

31 dicembre 2025

Completamento dello studio (Effettivo)

31 dicembre 2025

Date di iscrizione allo studio

Primo inviato

8 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 maggio 2026

Primo Inserito (Effettivo)

19 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

19 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2289\2024\19 (Altro numero di sovvenzione/finanziamento: The University of Jordan, Deanship of Scientific Research)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

Descrizione del piano IPD

all, except identifying information. Based on reasonable request.

Periodo di condivisione IPD

time of official publication to May 8th 2029

Criteri di accesso alla condivisione IPD

from any researcher from any country. They will be able to access all but identifying information. access is through contacting the corresponding author.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • ICF
  • CODICE_ANALITICO
  • RSI

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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