Before Colonoscopy Effect of Virtual Reality Application on Anxiety &

Status Recruiting

Clinical Trial Summary

This study was planned to examine the effect of virtual reality application on the patient's 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.

Clinical Trial Description

After obtaining the ethics committee and institutional permission for the research, the researcher was taken to the hospital for the colonoscopy procedure. He/she will introduce himself/herself 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 Design

Related Conditions & MeSH terms

Colonoscopy

Clinical Trial Details

NCT number	NCT06407531
Study type	Interventional
Source	Akdeniz University
Contact	Seda Cansu Yenigün, PhD
Phone	05077286208
Email	seda.cansu.yenigun@gmail.com
Status	Recruiting
Phase	N/A
Start date	November 21, 2023
Completion date	June 30, 2024

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Before Colonoscopy Effect of Virtual Reality Application on Anxiety and Vital Signs

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms