Pre-Anesthesia Visit: Analysis of Coverage Rate of Visit Content and Surgical Patients' Understanding of Information (Pre-Anesthesia)

December 11, 2024 updated by: Anshi Wu

Pre-Anesthesia Visit: Analysis of Coverage Rate of Pre-Anesthesia Visit Content by Anesthesiology Residents, and Surgical Patients' Understanding of Pre-Anesthesia Visit Information

The aim of this study was to systematically assess the coverage of anesthesiology residents' explanations of the content of the visit during the preoperative anesthesia visit and the patients' understanding of the content of the anesthesia approach through the physician's explanations.

Study Overview

Detailed Description

Physician Component:

In order to minimize the change of the interview content due to third-party supervision, the collected data were analyzed in the form of a questionnaire about the content of the visit after the preoperative visit by anesthesiology residents, including the main content of the visit, the duration of the visit, and the presumed level of patient's understanding of the anesthesia informed consent form.

Patient section:

To investigate the degree of patients' understanding of the contents of the anesthesia visit after listening to the visit. A questionnaire was used to collect the data, which included the content of the visit that the patients could recall, their level of understanding of the content explained by the physician, their concerns, and suggestions for improvement that could be taken to promote patient understanding.

Study Type

Observational

Enrollment (Estimated)

110

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Beijing
      • Beijing, Beijing, China, 100020
        • Recruiting
        • Beijing Chao-Yang Hospital
        • Contact:

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

No

Sampling Method

Non-Probability Sample

Study Population

  1. Age stratification of enrolled subjects, 18-80 years [young adults (18-35 years), middle-aged adults (36-60 years), older adults (61-80 years)];
  2. Stratification of subjects' educational attainment as elementary, middle school, high school, college

Description

Inclusion Criteria:

  • ASA I-II
  • Patients who have not previously undergone surgery under general anesthesia
  • Patients undergoing laparoscopic cholecystectomy or laparoscopic appendectomy

Exclusion Criteria:

  • Subjects who do not wish to participate in this study
  • Patients with visual or auditory impairment
  • Patients who are completely unable to understand the content of the communication or have communication difficulties

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

Cohorts and Interventions

Group / Cohort
Observation Group

To investigate patients' understanding of the content of the anesthesia visit after listening to the visit. A questionnaire was used to collect data.

The questionnaire included the contents of the visit that the patients could recall, their understanding of the physician's explanation, their concerns, and their suggestions for improving the preoperative visit.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patients' understanding of the content related to anesthesia visit after the preoperative visit with anesthesiology residents
Time Frame: Postoperative visit (one day after surgery)
Overall patient understanding of the anesthesia visit content was assessed by a patient self-measurement scale in the form of a rank variable, with 1 being no understanding at all and 5 being full understanding
Postoperative visit (one day after surgery)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient recall of what anesthesiology residents mentioned during the preoperative visit vs. what anesthesiology residents mentioned during the preoperative visit
Time Frame: resident-side:Pre-operative visit-one day before surgery;patient-side:Post-operative visit-one day after surgery
Differences in the content of the preoperative visit as recalled by the patient and the content of the modality as mentioned by the resident through resident-side and patient-side question and answer scales
resident-side:Pre-operative visit-one day before surgery;patient-side:Post-operative visit-one day after surgery
Stratified analysis of subjects according to different age/education levels to explore the relevance in understanding the content of the preoperative visit for anesthesia
Time Frame: Postoperative visit (one day after surgery)
  1. Age stratification as young adults (18-35 years), middle-aged adults (36-60 years), older adults (61-80 years);
  2. Stratification of subjects' educational attainment as elementary, middle school, high school, college.
Postoperative visit (one day after surgery)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patient concerns in the content of the preoperative approach
Time Frame: Postoperative visit (one day after surgery)
Understanding what worries patients most about anesthesia-related content during the preoperative visit
Postoperative visit (one day after surgery)
Patients' suggestions for improving the efficiency of preoperative anesthesia visits
Time Frame: Postoperative visit (one day after surgery)
Understanding what patients would like to take to promote understanding of the content of the preoperative visit from the patient's end of the spectrum
Postoperative visit (one day after surgery)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Lina Yang

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)

December 1, 2024

Primary Completion (Estimated)

December 30, 2025

Study Completion (Estimated)

December 30, 2025

Study Registration Dates

First Submitted

December 11, 2024

First Submitted That Met QC Criteria

December 11, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 11, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • PAV20241212
  • Pre-Anesthesia Visit (Registry Identifier: PAV20241212)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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