Ignite Creation Date:
2024-06-16 @ 11:51 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06441149
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-04
First Post:
2024-05-29
Brief Title:
Individualized Data-based High Simulation of Bronchoscopy Operations in Preoperative Bronchoscopy Informed Consent
Sponsor:
China-Japan Friendship Hospital
Organization:
China-Japan Friendship Hospital
Study Overview
Official Title:
The Impact of a Personalized Data-Based Bronchoscopy Simulation Operation System on Perioperative Anxiety and Satisfaction in Bronchoscopya Randomised Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
A prospective randomized controlled study was conducted to investigate whether preoperative replacement of patients based on AI training instruments could alleviate preoperative anxiety
Patients who met the criteria were randomly assigned to either the personalized data-based group or the control group Prior to the preoperative account examination each patients anxiety level was assessed after which a 30-40-minute informed consent form was read
The traditional group underwent a preoperative account and question-and-answer session with an experienced bronchoscopy laboratory physician after which the scale was reassessed
The experimental group underwent a simulated surgical procedure on an AI simulation instrument based on the patients CT personalized data performed by an experienced bronchoscopist The bronchoscopist explained the surgical precautions and answered the patients questions throughout the procedure Following the responses to the questions the scale was reassessed Following surgery patients are invited to complete a satisfaction survey prior to discharge or following the discussion of bronchoscopy findings
Patients who met the criteria were randomly assigned to either the personalized data-based group or the control group Prior to the preoperative account examination each patients anxiety level was assessed after which a 30-40-minute informed consent form was read
The traditional group underwent a preoperative account and question-and-answer session with an experienced bronchoscopy laboratory physician after which the scale was reassessed
The experimental group underwent a simulated surgical procedure on an AI simulation instrument based on the patients CT personalized data performed by an experienced bronchoscopist The bronchoscopist explained the surgical precautions and answered the patients questions throughout the procedure Following the responses to the questions the scale was reassessed Following surgery patients are invited to complete a satisfaction survey prior to discharge or following the discussion of bronchoscopy findings
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None