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Not yet recruiting NCT06980467

Evaluation of AI-Generated Clinical Advice by Physicians

No phase Interventional Artificial Intelligence (AI)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Large Language Model.
Who it may be relevant to
Registry conditions: Artificial Intelligence (AI). Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Study on the Evaluation of Artificial Intelligence-Generated Clinical Advisory Outputs in Medical Professional Contexts

Overview

This study examines how artificial intelligence systems interact with medical professionals. Researchers will compare physician responses to different AI-generated outputs in simulative medical scenarios.

Interventions

  • Other Large Language Model
    An artificial intelligence system generating clinical recommendations using prompts, designed to simulate clinical advisory outputs. The protocol focuses on structured medical language generation.

Primary outcome measures

  • Physician Response to AI-Generated Medical Content [Time frame: Through study completion, an average of 1 week]
Secondary outcome measures (1)
  • Physician Perception of Communication Quality in AI-Generated Content [Time frame: Through study completion, an average of 1 week]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years old;
  • Licensed physician or medical professional qualified to perform clinical evaluations;
  • Willing to sign informed consent and commit time to participate in the study.

Exclusion criteria

  • Unable to dedicate sufficient time to complete the study tasks;
  • Unable or unwilling to understand and follow study instructions.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Crossover
Masking
Single blind
Primary purpose
Other

Study locations

China · 2 centers
  • Tsinghua University — Beijing
  • Shanghai Health and Medical Center — Wuxi

Identifiers

NCT: NCT06980467 · 2025-07

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗