The Effect of Virtual Reality Based Relaxation Program on Patients to be Performed Bronchoscopy

NCT ID: NCT05154916

Last Updated: 2023-07-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-11-01
• Study Completion Date: 2022-05-01

Brief Summary

With the virtual reality application in patients with bronchoscopy, it is aimed to reduce the fear, stress and tension arising from the possibility of the development of pain and complications in the patients. The research will be carried out in the form of pretest-posttest application with 30 experimental and 30 control groups. The researcher aims to minimize the fear and stress in the patient by applying the virtual reality application to the patient in the experimental group 10 minutes before the procedure and 5-10 minutes during the procedure. The researcher will download the licensed program called 'a walk on the beach' to the virtual reality glasses and the patient will watch this program with glasses. The patient in the experimental group will have to fill in the Visual Analogue Scale, Anxiety Evaluation Form, Anxiety Symptoms Follow-up Form, and Patient Information Form before the procedure. 10-15 minutes after the procedure, the patient will be asked to fill the Visual Analogue Scale, Anxiety Evaluation Form, Anxiety Symptoms Follow-up Form and the Virtual Reality Glasses Application Satisfaction Form. No procedure will be applied to the patients in the control group and they will be asked to fill in the Patient Information Form, Visual Analogue Scale Form, Anxiety Evaluation Scale Form, and Anxiety Symptoms Follow-up Form before the procedure. After the procedure, he will be asked to fill in the other forms again, except the Patient Information Form. Patients over the age of 18, who have no communication problems, no psychiatric problems, who volunteered to participate in the study, and who had local application in bronchoscopy will be included in the study. Patients with psychiatric problems and communication problems will not be included in the study. Before the procedure, the patient will be informed that his/her identity information will be kept confidential and that he/she can withdraw from the research at any time, and all his/her rights will be informed.

Detailed Description

This study includes the examination of the effect of applying virtual reality interventions, which are used for the treatment of anxiety problems, to patients who will undergo bronchoscopy. For this purpose, first of all, a relaxation intervention will be designed in a virtual reality environment. The virtual reality environment will be organized on the basis of relaxation exercise. In this direction, first of all, an image will be created by taking 3D modeling service and the text of the relaxation exercise prepared in the presence of a professional sound artist will be transferred to the image with sound. Afterwards, the relaxation exercise created will be applied to the patients before and during the bronchoscopy application. The aim of this study; It is aimed to examine the Effect of Virtual Reality Based Relaxation Program on Pain Severity, Anxiety Level and Patient Satisfaction in Patients to be Performed Bronchoscopy.

Conditions

Bronchoscopy; Virtual Reality; Glasses; Relaxation Program

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: SINGLE

Study Groups

Experimental:

Bronchoscopy of Virtual Reality Based Relaxation Program Will Be Applied

Group Type: EXPERIMENTAL

Virtual Reality Based Relaxation Program

Intervention Type: OTHER

Virtual Reality Based Relaxation Program

No Intervention

Bronchoscopy of Virtual Reality Based Relaxation Program Will Not Be Applied

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Virtual Reality Based Relaxation Program

Virtual Reality Based Relaxation Program

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• be18 years and over
• Ability to communicate adequately
• Absence of psychiatric problems
• Those who are determined by the physician that they do not have a physical disability in exercising
• Volunteering to participate in the research
• Individuals who have the ability to use technological tools
• Patients who underwent local application in bronchoscopy

Exclusion Criteria

• Those who have communication problems
• Those with psychiatric problems

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Ataturk University

OTHER

Sponsor Role: lead

Responsible Party

gülcan bahcecioğlu

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Gülcan B Turan

Role: STUDY_CHAIR

Firat University

Locations

Fırat university

Elâzığ, Center, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

E-97132852-050.01.04-87889

Identifier Type: -

Identifier Source: org_study_id