Retrieval augmented generation for 10 large language models and its generalizability in assessing medical fitness.
Yu He Ke, Liyuan Jin, Kabilan Elangovan...
https://pubmed.ncbi.nlm.nih.gov/40185842Actively Recruiting
Led by Singapore General Hospital · Updated on 2026-05-07
120
Participants Needed
2
Research Sites
N/A
Total Duration
Researchers are evaluating the PEAR (Patient Education of Anaesthesia Risks) chatbot, a multilingual, AI-driven tool designed to improve patient understanding of anaesthesia risks during the consent process. The trial compares this digital method to the traditional face-to-face verbal consent provided by anaesthetists. PEAR aims to enhance patient education, satisfaction, and reduce preoperative anxiety while supporting clinician workflow without altering standard care. Participants undergoing elective surgery will be randomly assigned to either the PEAR chatbot intervention or the standard verbal consent control group. Those in the intervention group interact with the chatbot prior to meeting their anaesthetist, receiving personalized, interactive education on anaesthesia risks and procedures. The control group receives usual face-to-face counselling by a licensed anaesthetist following institutional protocols. Both groups eventually meet their anaesthetist to ensure clinical oversight. During the study visit, participants complete quizzes and surveys to assess understanding, satisfaction, and anxiety levels. Clinicians record the time and workload involved in each consent method. Data is collected electronically and stored securely. The main outcome measured is patient self-reported understanding of anaesthesia risks immediately after the PEAR interaction. The trial runs until April 2026, including assessments of perceived usefulness, ease of use, cost effectiveness, and behavioral intentions regarding the chatbot.
CONDITIONS
Effectiveness of Large Language Model for Anaesthesia and Procedural Consent
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single clinic visit
Participants receive anaesthesia risk counselling either through the PEAR chatbot before their face-to-face consultation with an anaesthetist or via the standard face-to-face verbal consent process.
1 visit (in-person)
Duration - Same day as treatment
Participants complete questionnaires and assessments immediately after the consent process to evaluate understanding, satisfaction, and anxiety.
1 visit (in-person, immediately post-consent)
Total: 2 locations
1
Singapore General Hospital
Singapore, Singapore, Singapore, 249094
Actively Recruiting
2
Singapore General Hospital
Singapore, Singapore, Singapore, 751126
Not Yet Recruiting
Y
Yuhe Ke, MMED (ANES)
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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Yu He Ke, Liyuan Jin, Kabilan Elangovan...
https://pubmed.ncbi.nlm.nih.gov/40185842