Virtual Reality Application on Pain Intensity and Anxiety Level in Endoscopy Patients

Anxiety Clinical Trial

Official title:

The Effect of Virtual Reality Application on Pain Intensity and Anxiety Level in Endoscopy Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05585749
• Other study ID #: 2022/ 04 - 22
• Status: Completed
• Phase: N/A
• Start date: September 5, 2022
• Est. completion date: June 30, 2023

Study information

• Verified date: January 2024
• Source: Ataturk University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 78
• Est. completion date: June 30, 2023
• Est. primary completion date: January 30, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

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 Exclusion Criteria: Those who have communication problems
• Those with psychiatric problems

Related Conditions & MeSH terms

• Anxiety
• Anxiety Disorders
• Pain

Intervention

Other:
• Virtual Reality Based Relaxation Program
Virtual Reality Based Relaxation Program

Locations

Country	Name	City	State
Turkey	Firat University	Elazig

Sponsors (1)

Lead Sponsor	Collaborator
Ataturk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Analog Scale	Visual Analog Scale is used to convert some values that cannot be measured numerically into digital. Two end definitions of the parameter to be evaluated are written at the two ends of a 100 mm line and the patient is asked to indicate where on this line their situation is appropriate by drawing a line or by placing a dot or pointing.0 points means no pain, 100 points means a lot of pain	1 hours later
Primary	Anxiety Assessment Scale	Patients will be asked to show their anxiety levels before and after the procedure on a 10 cm long horizontal line. Line has 0 at the beginning and 10 at the end. 10 means very extreme anxiety and 0 means no anxiety.	1 hours later
Primary	Physiological Symptoms of Anxiety Follow-up Form	This form was created by the researcher to record blood pressure, heart rate, respiratory rate and peripheral oxygen saturation value.	1 hours later