- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07304908
Effect of Perception-based Interventions on Public Acceptance of Using Large Language Models in Medicine
December 11, 2025 updated by: Liu Jue, Peking University
Perception-based Interventions Affect Public Acceptance of Using Large Language Models in Medicine: Randomized Controlled Trial
Large language models (LLMs) show promise in medicine, but concerns about their accuracy, coherence, transparency, and ethics remain.
To date, public perceptions on using LLMs in medicine and whether they play a role in the acceptability of health care applications of LLMs are not yet fully understood.
This study aims to investigate public perceptions on using LLMs in medicine and if interventions for perceptions affect the acceptability of health care applications of LLMs.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Detailed Description
Owing to rapid advances in artificial intelligence, large language models (LLMs) are increasingly being used in a variety of clinical settings such as triage, disease diagnosis, treatment planning, and self-monitoring.
Despite their potential, the use of LLMs remains restricted within healthcare settings due to lack of accuracy, coherence, and transparency and ethical concerns.
Public perceptions such as perceived usefulness and risks play a crucial role in shaping their attitudes towards artificial intelligence that can either facilitate or hinder its adoption.
Yet, to our knowledge, there is lack of awareness about perception-driven interventions in health care and no previous studies have examined whether public perceptions play a role in the acceptability of medical applications of LLMs.
Hence, this study aims to investigate public perceptions on using LLMs in medicine and if interventions for perceptions affect the acceptability of health care applications of LLMs.
Study Type
Interventional
Enrollment (Estimated)
3000
Phase
- Not Applicable
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
-
-
Beijing Municipality
-
Beijing, Beijing Municipality, China, 100191
- Jue Liu
-
-
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
Description
Inclusion Criteria:
- ≥18 years
- Capable of completing an online survey
- Agree to sign an informed consent form
Exclusion Criteria:
- Unable to answer questions or communicate
- Not willing to participate in this study
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
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
No intervention
|
|
|
Experimental: Perceived benefits of large language models in medicine
Participants were asked to read "In April 2023, Massachusetts General Hospital launched a pilot program utilizing medical LLMs to assist with emergency department triage and initial diagnosis and observed a reduction in patient wait times and an improvement in clinical efficiency."
|
Participants allocated to the intervention group received perception-based interventions.
Interventions for Groups 1-3 were perceived benefits of LLMs in medicine, perceived racial bias in LLMs in medicine, and perceived ethical conflicts in LLMs in medicine, respectively.
|
|
Experimental: Perceived racial bias in large language models in medicine
Participants were asked to read "In November 2022, a research team from the University of California, San Francisco found that cutting-edge medical LLMs exhibited racial bias when recommending treatment plans."
|
Participants allocated to the intervention group received perception-based interventions.
Interventions for Groups 1-3 were perceived benefits of LLMs in medicine, perceived racial bias in LLMs in medicine, and perceived ethical conflicts in LLMs in medicine, respectively.
|
|
Experimental: Perceived ethical conflicts in large language models in medicine
Participants were required to read "In February 2023, a major European hospital network inadvertently leaked partially anonymized but still sensitive patient data during the testing of medical LLMs due to a system configuration error.
Although no direct patient harm occurred, this increased public concerns regarding data privacy and security and compelled relevant institutions to conduct urgent reviews of their data protection measures."
|
Participants allocated to the intervention group received perception-based interventions.
Interventions for Groups 1-3 were perceived benefits of LLMs in medicine, perceived racial bias in LLMs in medicine, and perceived ethical conflicts in LLMs in medicine, respectively.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of participants who will change their attitudes towards medical applications of large language models
Time Frame: Through study completion, an average of 1 year
|
Public acceptance of applying large language models to medicine will be categorized into yes, not sure, and no, which will be collected before perception-based interventions and after interventions.
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Jue Liu, Peking University
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 (Actual)
November 25, 2025
Primary Completion (Estimated)
October 31, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
December 1, 2025
First Submitted That Met QC Criteria
December 11, 2025
First Posted (Actual)
December 26, 2025
Study Record Updates
Last Update Posted (Actual)
December 26, 2025
Last Update Submitted That Met QC Criteria
December 11, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NNSF72474005
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.
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