Actively Recruiting

Phase Not Applicable
Age: 21Years - 99Years
All Genders
Healthy Volunteers
ID06949462

Evaluating the Effectiveness of Large Language Models in Anaesthesia and Procedural Consent: A Comparative Analysis With Traditional Patient Consent Methods

Led by Singapore General Hospital · Updated on 2026-05-07

120

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Effectiveness of Large Language Model for Anaesthesia and Procedural Consent

Who Can Participate

Age: 21Years - 99Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (≥21 years old) undergoing elective surgery requiring anaesthesia
  • Classified as ASA Physical Status I to III
  • Able to provide informed consent
  • Able to communicate effectively in English, Chinese (Mandarin), Malay, or Tamil
  • Willing and able to complete questionnaires and interact with the PEAR chatbot (intervention arm)
Not Eligible

You will not qualify if you...

  • ASA Physical Status IV or above
  • Cognitive impairment or psychiatric conditions that may limit comprehension or communication
  • Non-literate patients or those unable to understand English, Chinese, Malay, or Tamil
  • Emergency surgery cases
  • Prior participation in the study (to prevent bias)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Follow-up

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)

Trial Site Locations

Total: 2 locations

1

Singapore General Hospital

Singapore, Singapore, Singapore, 249094

Actively Recruiting

2

Singapore General Hospital

Singapore, Singapore, Singapore, 751126

Not Yet Recruiting

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Research Team

Y

Yuhe Ke, MMED (ANES)

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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