- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06735183
Pre-Anesthesia Visit: Analysis of Coverage Rate of Visit Content and Surgical Patients' Understanding of Information (Pre-Anesthesia)
Pre-Anesthesia Visit: Analysis of Coverage Rate of Pre-Anesthesia Visit Content by Anesthesiology Residents, and Surgical Patients' Understanding of Pre-Anesthesia Visit Information
Study Overview
Status
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
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Lina Yang
- Phone Number: 0086+18611635556
- Email: Thoth_safin@sina.com
Study Locations
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Beijing
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Beijing, Beijing, China, 100020
- Recruiting
- Beijing Chao-Yang Hospital
-
Contact:
- Lina Yang
- Phone Number: 18611635556
- Email: Thoth_safin@sina.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
- Age stratification of enrolled subjects, 18-80 years [young adults (18-35 years), middle-aged adults (36-60 years), older adults (61-80 years)];
- 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
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
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resident-side:Pre-operative visit-one day before surgery;patient-side:Post-operative visit-one day after surgery
|
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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)
|
|
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
Sponsor
Investigators
- Study Director: Lina Yang
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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