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Impact of GPT-4-Generated Discharge Letters on Patients' Medical Comprehension: Prospective Crossover Study

Holderried F, Sonanini A, Stegemann-Philipps C, Herrmann-Werner A, Spitzer P, Guthoff M, Heyne N, Sering K et al.

Journal of medical Internet research, 2026

48 participants · 3 citations

Abstract

Background: Patients often struggle to understand standard hospital discharge letters, increasing the risk of medication errors and misunderstandings. According to cognitive load theory (CLT), complex, information-dense texts can overload working memory and impair comprehension. Artificial intelligence tools that generate patient-centered versions could help reduce extraneous cognitive load and bridge this gap. However, evidence for their effectiveness remains limited.

Objective: This study aimed to evaluate whether GPT-4 (OpenAI)-generated patient-centered letters improve standardized patients' retention and understanding of safety-relevant medical information compared with standard hospital discharge letters, and to explore potential effects on cognitive load as described by CLT.

Methods: In this prospective, randomized, crossover study, 48 trained standardized patients received a conventional discharge letter for an assigned disease (out of 3) and its matching GPT-4-generated patient-centered letter. Participants read one version first, identified predefined safety-relevant "learning objectives," and then repeated the task with the alternate version. The primary outcome was the proportion of learning objectives fully, partially, or not reported. In a secondary analysis, results were stratified by content field (Medication, Organization, Prevention of Complications, Lifestyle/Disease Management) and Bloom taxonomy level ("Remember," "Understand").

Results: The letter type…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 48 participants or records.

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