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Clinical Trials in China / NCT07647536
Active, not recruiting Not applicable

LLMs Improve Patient Understanding of Ultrasound Reports

NCT07647536 · tracked via the Priya Life Science China tracker
Sponsor
Lu Wang
Phase
Not applicable
Started
2026-06-01
Last updated
2026-06-15

Condition(s) studied

Patient Understanding of Ultrasound Reports

Investigational drug(s) / intervention(s)

Standard ultrasound report presentationExpert-reviewed AI-simplified ultrasound report presentation

Standard ultrasound report presentation: Presentation of the completed routine ultrasound report to the participant or legal guardian

Expert-reviewed AI-simplified ultrasound report presentation: Presentation of a patient-facing plain-language ultrasound report generated by an AI workflow and reviewed by ultrasound physicians before participant or guardian exposure. The intervention did not alter ultrasound acquisition, diagnostic interpretation, treatment decisions, follow-up, or clinical management

Study summary

This multicenter, patient-blinded, controlled evaluation assessed whether expert-reviewed artificial intelligence (AI)-simplified ultrasound reports improved patient- or guardian-reported understanding and reading experience compared with standard ultrasound reports. Routine ultrasound reports were completed through existing clinical processes. After completion of the routine report, participants were assigned to view either the standard report or an expert-reviewed plain-language version generated with a large language model workflow.

The simplified report was intended only as a patient-facing communication aid. It did not replace the standard clinical report and did not alter ultrasound acquisition, diagnostic interpretation, treatment decisions, follow-up, or subsequent clinical management. Patient- or guardian-reported outcomes included cognitive workload, comprehension, report perception, and reading time. Expert review assessed whether AI-generated simplified reports preserved source meaning and identified factual errors, omissions, or unsupported additions before patient presentation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Patients receiving an ultrasound report at a participating center. Adult participants able to provide written informed consent. For participants younger than 18 years, a legal guardian able to provide written informed consent, read the assigned report, and complete the questionnaire. Participants or legal guardians able to read one assigned report presentation format and complete the study questionnaire immediately after reading. Exclusion Criteria: * Refusal or inability to provide written informed consent by the adult participant or legal guardian. Inability of the participant or legal guardian to read the assigned report presentation format or complete the questionnaire. Incomplete evaluation, including missing responses to any of the nine rating items or the reading-time item. Missing key study information required for analysis, including participating center or assigned report presentation format.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sichuan cancer hospital Chengdu Sichuan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07647536 on ClinicalTrials.gov ↗ ← All trials in China