Determining the Consistency Between Nurses and Artificial Intelligence (ChatGPT-5) in Delivering Scenario-Based Discharge Education to Coronary Artery Bypass Graft Patients: A Methodological Study

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHasan Kalyoncu University

About this trial

This methodological study aims to determine the level of agreement between nurses and an artificial intelligence system (ChatGPT-4.0) in providing scenario-based discharge education for patients who have undergone coronary artery bypass graft (CABG) surgery. Thirty standardized patient scenarios representing different demographic, clinical, and psychosocial characteristics will be used. For each scenario, both expert nurses and ChatGPT-4.0 will prepare discharge education content based on six main domains and twenty-four subtopics identified from the literature and clinical guidelines. The educational materials will be independently evaluated by two blinded reviewers in terms of content accuracy, completeness, scientific consistency, and clarity of language. Agreement between nurses and AI-generated content will be analyzed using Cohen's Kappa coefficient and Fisher's Exact Test. The findings are expected to provide evidence for the reliability and applicability of AI-assisted discharge education systems in cardiac surgery nursing practice.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patient scenarios representing individuals who have undergone coronary artery bypass graft (CABG) surgery.

Scenarios that include demographic, socioeconomic, clinical, and psychosocial information consistent with current literature and clinical guidelines.

Scenarios describing patients who underwent median sternotomy and on-pump CABG procedure.

Scenarios that include relevant postoperative complications (e.g., delirium, bleeding, wound infection, arrhythmia) and comorbidities (e.g., diabetes, hypertension, COPD).

Disqualifiers

Patient scenarios not related to coronary artery bypass graft (CABG) surgery.

Scenarios lacking sufficient demographic, clinical, or psychosocial information to prepare individualized discharge education.

Scenarios that do not follow the standardized structure of six main domains and twenty-four subtopics.

Scenarios with inconsistent or contradictory medical data (e.g., incompatible diagnosis and treatment details).

Trial population

Çalışma evreni, koroner arter bypass grefti (CABG) ameliyatı geçirmiş bireyleri temsil eden 30 standart hasta senaryosundan oluşmaktadır. Her bir senaryo, CABG sonrası hastalarda yaygın olarak gözlemlenen demografik, klinik ve psikososyal özelliklerin özgün bir kombinasyonunu yansıtmaktadır. Senaryolar, klinik gerçekliği ve içerik geçerliliğini sağlamak amacıyla kalp damar cerrahisi hemşireleri, akademik hemşirelik uzmanları ve kardiyovasküler cerrahların yer aldığı multidisipliner bir ekip tarafından geliştirilmiş ve doğrulanmıştır. Bu simüle edilmiş vakalar, hem hemşireler hem de ChatGPT-5 tarafından hazırlanan taburculuk eğitimi materyalleri arasındaki uyumu değerlendirmek için gözlem birimleri olarak kullanılacaktır.

Trial design

Design model

Other

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

30 Participants
are grouped into 2 trial groups
Group A: Nurse-Provided Discharge Education
Group B: ChatGPT-5-Generated Discharge Education

Trial outcomes

Primary outcomes

1

Agreement Between Nurse- and ChatGPT-5-Generated Discharge Education Content

The level of agreement between discharge education materials prepared by cardiovascular surgery nurses and those generated by ChatGPT-5 for standardized post-CABG patient scenarios.

Time frame
During data collection (expected within 8 months after study start).
2

Agreement Between Nurse- and ChatGPT-5-Generated Discharge Education Content

The level of agreement between discharge education materials prepared by cardiovascular surgery nurses and those generated by ChatGPT-5 for standardized post-CABG patient scenarios.

Time frame
During data collection (expected within 12 months after study start).

Secondary outcomes

Other outcomes

Sponsors and contacts

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