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Scientific Validity Assessment and Optimization of AI-Generated A3/A4 Type Questions for the Chinese Medical Licensing Examination

Scientific Validity Assessment and Optimization of AI-Generated A3/A4 Type Questions for the Chinese Medical Licensing Examination: An Empirical Analysis Based on the "Answering-Generating" Closed Loop and Transformation of Competency Assessment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07505862
Enrollment
20
Registered
2026-04-01
Start date
2025-10-01
Completion date
2026-03-30
Last updated
2026-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AI (Artificial Intelligence)

Brief summary

This is a cross-sectional study that primarily employs quantitative analysis, supplemented by qualitative assessment. The research is conducted in two stages: Phase I consists of a model performance comparison experiment, and Phase II involves an item quality evaluation experiment. The entire study adheres to the principles of single-blinding, randomization, and standardization to ensure scientific rigor and reproducibility. The single-blind design is implemented during the "standardized testing" phase, where the system intersperses AI-generated items with those authored by human experts. Participants remain blinded to the source of each item (AI-generated vs. human-authored) throughout the testing and scoring processes, thereby ensuring the objectivity of the evaluation results.

Interventions

None listed

Sponsors

Guangdong Provincial People's Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* 1.Professional Status: Medical students currently enrolled in a Standardized Residency Training (SRT) program. 2.Educational Background: Holders of a Bachelor of Medicine degree or higher, with foundational clinical knowledge. 3.Informed Consent: Voluntarily participate in the study and provide written informed consent. 4.Technical Competency: Proficient in using digital platforms to complete assessments and scoring.

Exclusion criteria

* 1.Conflict of Interest: Individuals involved in the AI model training, prompt engineering, or the creation of the human-authored question bank for this study. 2.Inability to Complete: Presence of visual/auditory impairments or severe illness that precludes completion of the assessment within the specified time. 3.Investigator's Discretion: Any other condition that, in the opinion of the investigator, renders the participant unsuitable for the study.

Design outcomes

Primary

MeasureTime frameDescription
Comparative Analysis of Item AccuracyBaselineThe investigators will evaluate the average accuracy rates coefficients of AI-generated items compared to human-generated items

Countries

China

Contacts

CONTACTZhuoyi Chen MD
18737552662@163.com+86 18737552662

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026