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Clinical Trials/NCT06652854
NCT06652854Not yet recruitingNot Applicable

Implementation of Large Language Models in Anesthesia to Answer Patients' Questions During Pre-Anesthesia Visits: A Prospective, Observational Study

Ottawa Hospital Research Institute1 site in 1 country190 target enrollmentStarted: December 9, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
190
Locations
1
Primary Endpoint
knowledge

Study Overview

Brief Summary

Patients are waiting for surgery longer than ever before. While hospitals are trying to get patients access to surgery as quickly as possible, a shortage of anesthesia doctors (called anesthesiologists) prevents this. Every surgery needs an anesthesiologist, but anesthesiologists also assess patients beforehand to ensure they can safely undergo surgery and help patients understand what to expect and the risks involved. Ensuring that patients move through surgery as safely and efficiently as possible requires that the limited number of anesthesiologists in Canada work as efficiently as possible. Technology like Artificial Intelligence (AI), in programs such as ChatGPT, might assist by answering common questions patients have, allowing anesthesiologists to focus their limited time on addressing complex and personalized issues for each patient. However, studies conducted so far on how well AI can answer questions about anesthesia and surgery have been poorly designed and have not included patients as members of the research team. This study will determine whether AI can answer patients' questions before surgery as effectively as both patients and expert anesthesiologists would expect, which could be beneficial to patients and the healthcare system.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age > 18 years
  • Elective non-cardiac surgery
  • In-person preoperative anesthesiology consultation
  • Ability to participate and provide informed consent independently.

Exclusion Criteria

  • Unable to communicate in English or French
  • Nurse consultation only
  • Inclusion Criteria:
  • Anesthesiology residents or staff providing service at the PAU at TOH
  • Exclusion Criteria:
  • Anesthesiology residents or staff unwilling to participate in the research study.

Outcomes

Primary Outcomes

knowledge

Time Frame: From the date of the pre-anesthesia consultation until 2 weeks after the consultation, assessed over a period of up to 2 weeks post-consultation

Patients will be blinded to the source of the two responses (GPT-4 and Anesthesiologist). After reading both responses, they will complete a questionnaire that includes an 11-point Likert-scale question for the primary outcome of knowledge: "To what extent does the response address the knowledge or information you hoped to gain?" (0 = not at all addressed; 10 = fully addressed)

Secondary Outcomes

  • Patient satisfaction(From the date of the pre-anesthesia consultation until 2 weeks after the consultation, assessed over a period of up to 2 weeks post-consultation)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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