Ignite Creation Date:
2024-05-06 @ 8:14 PM
Last Modification Date:
2024-10-26 @ 3:23 PM
Study NCT ID:
NCT06309108
Status:
COMPLETED
Last Update Posted:
2024-03-13
First Post:
2023-12-15
Brief Title:
Bariatric Surgery and Patient Education
Sponsor:
Istanbul University - Cerrahpasa IUC
Organization:
Istanbul University - Cerrahpasa IUC
Study Overview
Official Title:
The Effect of Education Given to Patients With Two Different Materials Before Bariatric Surgery on Early Complications
Status:
COMPLETED
Status Verified Date:
2024-03
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:
Obesity is a disease that poses a health risk and is increasing worldwide Bariatric surgery is the most effective method used in the treatment of obesity Preoperative health education for bariatric surgery patients is important to support surgery There is not enough nursing research in the literature regarding training patients with two different materials before bariatric surgery The purpose of the randomized controlled experimental study designed in light of this information was to determine the effect of education given to patients with two different materials before bariatric surgery on early complications The rates of the study were determined by randomizing trial I trial II and control treatment in 66 rooms that met the interval and study screening criteria offered between May 2022 and June 2023 in the general surgery service of a university hospital Data from the research was collected with the Veria Total Form Autar Risk Assessment Scale Apfel Risk Score Visual Comparison Scale-VAS Visual Analog Scale-VAS Training Satisfaction Survey and Complication Monitoring Form In the first face-to-face meeting in the experimental groups we were given training by the researcher with the removable Training Booklet I and Training Booklet II and were monitored until discharge No control group training was given
Detailed Description:
Training Booklet Group Experimental Group I Patients who were eligible for the research were informed about the purpose content and method of the research by reading the volunteer information form and verbal and written permission was obtained from those who agreed to participate in the research voluntarily Before the surgery Part I of the Data Collection Form and the Autar Risk Assessment Scale were recorded in the form by the researcher Before the surgery the patients were given Educational Booklet I Patients questions about the booklet were answered The Education Satisfaction Survey was filled out by the patients in order to measure their satisfaction with the booklet When the patient is taken to the service after the surgery the Data Collection Form II III IV Part V Apfel Risk Score VAS and Complication Monitoring Form were evaluated and recorded until the patient was discharged
Augmented Reality Group Experiment II GROUP Patients who were eligible for the research were informed about the purpose content and method of the research by reading the voluntary information form and verbal and written permission was obtained from those who agreed to participate in the research voluntarily Before the surgery Part I of the Data Collection Form and the Autar Risk Assessment Scale were recorded in the form by the researcher Before the surgery the patients were given Educational Booklet II They were asked to install the 3DQR Plus application on their smartphones The patients ability to scan the QR code was checked Patients who could open and read the QR code and who could open 9 QR codes and see the augmented reality element were asked to fill out the Training Satisfaction Survey When the patient is taken to the service after the surgery the Data Collection Form II III IV and Part V Apfel Risk Score VAS and Complication Monitoring Form were evaluated and recorded until the patient was discharged
Control Group Patients Patients who were eligible for the study were informed about the purpose content and method of the study by reading the voluntary information form
Verbal and written permission was obtained from those who voluntarily agreed to participate in the study Control group patients were not given any training by the researcher and the service routine was applied Before the surgery Part I of the Data Collection Form and the Autar Risk Assessment Scale were recorded in the form by the researcher When the patient is taken to the service after the surgery the Data Collection Form II III IV and Part V Apfel Risk Score VAS and Complication Monitoring Form were evaluated and recorded until the patient was discharged
Augmented Reality Group Experiment II GROUP Patients who were eligible for the research were informed about the purpose content and method of the research by reading the voluntary information form and verbal and written permission was obtained from those who agreed to participate in the research voluntarily Before the surgery Part I of the Data Collection Form and the Autar Risk Assessment Scale were recorded in the form by the researcher Before the surgery the patients were given Educational Booklet II They were asked to install the 3DQR Plus application on their smartphones The patients ability to scan the QR code was checked Patients who could open and read the QR code and who could open 9 QR codes and see the augmented reality element were asked to fill out the Training Satisfaction Survey When the patient is taken to the service after the surgery the Data Collection Form II III IV and Part V Apfel Risk Score VAS and Complication Monitoring Form were evaluated and recorded until the patient was discharged
Control Group Patients Patients who were eligible for the study were informed about the purpose content and method of the study by reading the voluntary information form
Verbal and written permission was obtained from those who voluntarily agreed to participate in the study Control group patients were not given any training by the researcher and the service routine was applied Before the surgery Part I of the Data Collection Form and the Autar Risk Assessment Scale were recorded in the form by the researcher When the patient is taken to the service after the surgery the Data Collection Form II III IV and Part V Apfel Risk Score VAS and Complication Monitoring Form were evaluated and recorded until the patient was discharged
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
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| İUC | OTHER | İUC | None |