Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT06309108 |
| Other study ID # |
2022/68-04 |
| Secondary ID |
IUC |
| Status |
Completed |
| Phase |
N/A
|
| First received |
|
| Last updated |
|
| Start date |
January 2, 2022 |
| Est. completion date |
July 18, 2023 |
Study information
| Verified date |
March 2024 |
| Source |
Istanbul University - Cerrahpasa (IUC) |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial 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.
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 patient's 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.
