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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

110 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-12-01

Study Completion Date

2025-12-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

To Assess the Coverage of Anesthesiology Residents' Explanations of the Content of the Visit Patients' Understanding of the Content of the Anesthesia Approach Through the Physician's Explanations

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

preoperative anesthesia visit understanding of the content of the anesthesia approach

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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

Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Anshi Wu

Administrative Director of Anesthesiology

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Lina Yang

Role: STUDY_DIRECTOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Beijing Chao-Yang Hospital

Beijing, Beijing Municipality, China

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

China

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Lina Yang

Role: CONTACT

Phone: 0086+18611635556

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Lina Yang

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.