Generating Fast and Slow for Entree Level Medical Knowledge

February 14, 2024 updated by: National Taiwan University Hospital
The generative artificial intelligence tool, ChatGPT, has garnered widespread interest since its launch. This innovative multimedia platform has the potential to enhance medical communication and health education, thereby improving medical accessibility and reducing the burden on healthcare professionals. Some studies have indicated that ChatGPT achieves higher levels of satisfaction in counseling compared to human healthcare professionals. Additionally, research has shown that ChatGPT's performance in answering objective structured clinical examination questions is comparable to that of typical medical students. However, in both scenarios, it still requires editing by professionals before being used. Moreover, a recent meta-analysis evaluating ChatGPT's ability in various types of medical exams revealed inconsistent results. Before its application and actual integration into clinical practice, the investigators need to comprehend the advantages, disadvantages, and relevant limitations of ChatGPT in the field of medical communication. This study aims to simulate virtual consultations between ChatGPT, acting as a health professional, and study participants, serving as patients. It will evaluate the participants' satisfaction with the virtual consultation questions, categorized by different levels of cognition through Bloom's Taxonomy. This study plans to recruit medical professionals, healthcare-related professionals, medical students from National Taiwan University Hospital, and the general public. Two researchers will select 20 questions from the USMLE step 3 practice tests and the second stage of the Taiwan Medical Licensing Examination. These questions will be categorized into different levels of cognition based on knowledge, comprehension, application, analysis, synthesis, or evaluation. ChatGPT 3.5 and 4.0 will answer these 20 questions without specifying the question's level of cognition. Each participant will review the answers to these 20 questions and assign a satisfaction score based on the appropriateness of each answer.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

120

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The medical professionals, healthcare-related professionals, and medical students refer to attending physician, medical radiation technologist from National Taiwan University Hospital, and medical students from National Taiwan University College of Medicine, respectively. The general public refer to volunteers from Taiwan Emergency Medical Technician Association.

Description

Inclusion Criteria:

  1. National Taiwan University Hospital

    • Medical professionals
    • Healthcare-related professionals
    • Medical students
  2. Taiwan Emergency Medical Technician Association.

    • Volunteers

Exclusion Criteria:

  • N/A.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Medical professionals
Attending physicians of National Taiwan University Hospital
Participants will assign a satisfaction score based on the appropriateness of each answer.
Healthcare-related professionals
Medical Radiation Technologist of National Taiwan University Hospital
Participants will assign a satisfaction score based on the appropriateness of each answer.
Medical students
Medical students of National Taiwan University College of Medicine who have passed the first stage of Taiwan Medical Licencing Exam.
Participants will assign a satisfaction score based on the appropriateness of each answer.
General public
Volunteers from Taiwan Emergency Medical Technician Association
Participants will assign a satisfaction score based on the appropriateness of each answer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correlation between satisfaction and Bloom's taxonomy
Time Frame: baseline (at completion of study questionnaire)
Divided by the four participant groups
baseline (at completion of study questionnaire)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correctness of answers
Time Frame: baseline (at completion of study questionnaire)
Answers from ChatGPT 3.5/4.0 and the answers provided by Medical Licencing Exam institutions
baseline (at completion of study questionnaire)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

February 1, 2024

Primary Completion (Estimated)

June 1, 2024

Study Completion (Estimated)

June 1, 2024

Study Registration Dates

First Submitted

January 29, 2024

First Submitted That Met QC Criteria

February 6, 2024

First Posted (Actual)

February 8, 2024

Study Record Updates

Last Update Posted (Actual)

February 16, 2024

Last Update Submitted That Met QC Criteria

February 14, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 202308059RINB

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Data would be shared by request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Patient Satisfaction

Clinical Trials on Answers generated by ChatGPT

3
Subscribe