Viewing Study NCT06407531



Ignite Creation Date: 2024-05-11 @ 8:30 AM
Last Modification Date: 2024-10-26 @ 3:29 PM
Study NCT ID: NCT06407531
Status: COMPLETED
Last Update Posted: 2024-07-05
First Post: 2024-05-03

Brief Title: Before Colonoscopy Effect of Virtual Reality Application on Anxiety and Vital Signs
Sponsor: Akdeniz University
Organization: Akdeniz University

Study Overview

Official Title: Examining the Effect of Virtual Reality Application on Patients Anxiety and Vital Signs Before Colonoscopy A Randomized Controlled Study
Status: COMPLETED
Status Verified Date: 2024-07
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: This study was planned to examine the effect of virtual reality application on the patients anxiety and vital signs before colonoscopy The hypotheses of the research are as follows

H1 Virtual reality application before colonoscopy has an effect on patients anxiety and vital signs

H0 Virtual reality application before colonoscopy has no effect on patients anxiety and vital signs

Before colonoscopy patients in the study group will be asked to watch videos using virtual reality glasses
Detailed Description: After obtaining the ethics committee and institutional permission for the research the researcher was taken to the hospital for the colonoscopy procedure

Heshe will introduce himselfherself to the patients and explain the purpose of the research Patients who volunteered to participate in the study Informed consent will be obtained Data regarding the socio-demographic characteristics of the patients included in the patient introduction form The patient will be interviewed face to face and data regarding the patients clinical characteristics will be recorded from the patient file colonoscopy Data will begin to be collected from the first patient to undergo the procedure Anxiety and life assessment with VAS 30 minutes before the procedure The findings will be considered According to the randomization the patient in the virtual reality glasses group was first asked by the researcher

It will be explained to the patient that he will wear the glasses for 30 minutes and watch a video before the procedure By researcher 30 When the minute is up the patient will be informed and asked to remove the glasses No intervention was made to the patient in the control group

It will not be done Anxiety and vital signs were measured with VAS 5-10 minutes before the procedure began in all patient groups

will be looked into After each patient use the virtual reality glasses will be cleaned and dried with alcohol-based cleaning material

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