Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
190 participants
OBSERVATIONAL
2024-12-09
2025-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patient scheduled for a pre-surgery consultation with a physician anesthesiologist
After obtaining consent, patients will be asked to respond to the following query: "What is the most important question you had hoped to ask your anesthesiologist today about your anesthesia care, pain management or the time immediately around surgery?'.
No interventions assigned to this group
Specialty-trained anesthesiologists in independent practice within the pre-admission
anesthesiologists will be designated as either "response generators" or "response raters." Response generators will craft answers to patient queries, while response raters-anesthesiologists with over five years of clinical experience-will evaluate the quality of these responses.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* 1\. Age \> 18 years 2. Elective non-cardiac surgery 3. In-person preoperative anesthesiology consultation 4. Ability to participate and provide informed consent independently.
Anesthesiology residents or staff providing service at the PAU at TOH
Exclusion Criteria
Physicians
Anesthesiology residents or staff unwilling to participate in the research study.
18 Years
ALL
Yes
Sponsors
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Ottawa Hospital Research Institute
OTHER
Responsible Party
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Locations
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Ottawa Hospital Research Institute
Ottawa, Ontario, Canada
Countries
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Central Contacts
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Facility Contacts
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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20240526-01H
Identifier Type: -
Identifier Source: org_study_id
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