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Multi-Disciplinary Treatment on the Anthropomorphism of Large Language Models

Observational Cancer Respiratory Failure Heart Diseases Infections

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: GPT-4o, GPT-4o mini, MedicalGPT, Claude-3.5 Sonnet.
Who it may be relevant to
Registry conditions: Cancer, Respiratory Failure, Heart Diseases, Infections. Basic parameters: No limits · 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

Multi-Disciplinary Treatment on the Anthropomorphism of Large Language Models: A Parallel Controlled Study

Overview

This retrospective clinical trial aims to better explore the potential of large language models in medicine by comparing the effectiveness of MDT consultations conducted by human doctors with those conducted by large language models. The main questions to be addressed are: Does using large language models to conduct anthropomorphic MDT consultations yield better results than using non-anthropomorphic processes? Is there a significant performance gap between MDT consultations conducted by large language models and those conducted by humans? How much greater is the economic benefit of MDT consultations from large language models compared to those conducted by humans? Retrospectively collect MDT consultation records from the past 20 years in northern Sichuan in China, as well as anonymized patient medical records. Group 1: Different large language models are assigned to act as doctors from different departments and as MDT secretaries to summarize consultations. Group 2: The large language model directly outputs diagnostic and treatment recommendations for patients. Compare the outputs of groups 1 and 2 with human performance retrospectively, score them, and select the best model from each department for a re-evaluation through anthropomorphic MDT consultations, once again comparing them to human results.

Interventions

  • Diagnostic test GPT-4o
    Input all patient medical records, including text, examination reports, and imaging data, into GPT-4o. Use pre-tested prompts to establish department roles, enabling it to provide diagnostic and treatment recommendations pertinent to the respective department.
  • Diagnostic test GPT-4o mini
    Input all patient medical records, including text, examination reports, and imaging data, into GPT-4o mini. Use pre-tested prompts to establish department roles, enabling it to provide diagnostic and treatment recommendations pertinent to the respective department.
  • Diagnostic test MedicalGPT
    Input all patient medical records, including text, examination reports, and imaging data, into MedicalGPT. Use pre-tested prompts to establish department roles, enabling it to provide diagnostic and treatment recommendations pertinent to the respective department.
  • Diagnostic test Claude-3.5 Sonnet
    Input all patient medical records, including text, examination reports, and imaging data, into Claude-3.5 Sonnet. Use pre-tested prompts to establish department roles, enabling it to provide diagnostic and treatment recommendations pertinent to the respective department.
  • Diagnostic test Claude 3 Haiku
    Input all patient medical records, including text, examination reports, and imaging data, into Claude 3 Haiku. Use pre-tested prompts to establish department roles, enabling it to provide diagnostic and treatment recommendations pertinent to the respective department.
  • Diagnostic test Real Doctors
    Retrospectively collect the diagnostic and treatment recommendations from the corresponding departments involved in the multidisciplinary treatment of past patients, as well as the overall recommendations.

Primary outcome measures

  • Consultation Cost ($) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Consultation Time (min) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Comprehensiveness of the Multi-Disciplinary Treatment Results (Percentage Scale) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Clarity of Multi-Disciplinary Treatment Results (Percentage Scale) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Correctness of Multi-Disciplinary Treatment Results (Percentage Scale) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Cross-Professional Team Collaboration Practice Assessment (CPAT) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Rating Scale for Summarization [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
  • Flesch-Kincaid Readability Test [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]
Secondary outcome measures (1)
  • Ethical Compliance (Boolean) [Time frame: From Multi-Disciplinary Treatment Process to Multi-Disciplinary Treatment Process until all json fields are output, the time taken by human doctors to record the time using His system generally does not exceed 12 hours.]

Eligibility criteria

Inclusion criteria

  • 1\. The medical records include interdisciplinary consultation notes, with recommendations from specialists of various departments and a well-documented final summary.
  • 2\. The medical records contain data from at least one year prior to and one year following the consultation (including intact reports and imaging records).
  • 3\. The patient\'s discharge conditions improved due to the multidisciplinary treatment plan after the consultation.

Exclusion criteria

  • 1\. The medical records do not include multidisciplinary consultation notes, or the recommendations from various departmental physicians and the final summary notes are incomplete or inadequate.
  • 2\. The medical records lack data from 1 year before and after the consultation, or miss necessary reports and imaging data, resulting in incomplete documentation.
  • 3\. The patient\'s condition at discharge has not improved following the multidisciplinary treatment plan, or the condition has worsened.

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

Healthy volunteers: No

Study design

Observational model
Other

Study locations

China · 1 center
  • The Affiliated Hospital of North Sichuan Medical College — Nanchong

Publications

  • Schroder C, Medves J, Paterson M, Byrnes V, Chapman C, O'Riordan A, Pichora D, Kelly C. Development and pilot testing of the collaborative practice assessment tool. J Interprof Care. 2011 May;25(3):189-95. doi: 10.3109/13561820.2010.532620. Epub 2010 Dec 23. PMID 21182434

Identifiers

NCT: NCT06627985 · 1426887-2024-3

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗