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

14 de maio de 2026 atualizado por: 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).

Visão geral do estudo

Descrição detalhada

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 de estudo

Intervencional

Inscrição (Real)

268

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

      • Amman, Jordânia, 11942
        • The University of Jordan

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

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

Exclusion Criteria:

  • None

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Outro
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição cruzada
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.
Experimental: 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.
Experimental: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Emergency and Critical Care Nurses Proficiency in Computer Interpretation of the ECG
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Amer M Hasanien, PhD, The University of Jordan

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de fevereiro de 2025

Conclusão Primária (Real)

31 de dezembro de 2025

Conclusão do estudo (Real)

31 de dezembro de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

8 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de maio de 2026

Primeira postagem (Real)

19 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

14 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2289\2024\19 (Número de outro subsídio/financiamento: The University of Jordan, Deanship of Scientific Research)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

all, except identifying information. Based on reasonable request.

Prazo de Compartilhamento de IPD

time of official publication to May 8th 2029

Critérios de acesso de compartilhamento 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 de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • ANALYTIC_CODE
  • CSR

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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