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Clinical Trials/NCT05585749
NCT05585749CompletedNot Applicable

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

Ataturk University1 site in 1 country78 target enrollmentStarted: September 5, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
78
Locations
1
Primary Endpoint
Physiological Symptoms of Anxiety Follow-up Form

Study Overview

Brief Summary

In contemporary medicine, endoscopic procedures are often regarded as the gold standard for the diagnosis and treatment of gastrointestinal illnesses due to the essential role they play in these processes. Endoscopy is a minimally invasive procedure that allows direct visualization of the gastrointestinal tract using a flexible, camera-equipped instrument.However, due to their invasive nature, these methods pose certain challenges for both healthcare professionals and patients. In particular, the physical discomfort and pain experienced during the procedure can lead to a negative attitude toward the process in patients, which can indirectly affect the success of the procedure .Despite the fact that a number of studies have examined the impact of virtual reality applications on pain and anxiety during endoscopy, the conclusions remain inconsistent. Moreover, relatively few studies have assessed physiological signs of anxiety. Therefore, uncertainties remain regarding the generalizability of existing findings. The present study aimed to examine the effect of virtual reality application on pain, anxiety, and physiological parameters in patients undergoing endoscopy.

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Participant)

Masking Description

Virtual Reality Based Relaxation Program

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Eligible individuals were adults aged 18 or older, capable of effective communication, and scheduled for non-sedated oral gastroduodenoscopy (OGD).

Exclusion Criteria

  • •included emergency endoscopy, neurological conditions (e.g., migraine, vertigo, chronic headaches), or sensory impairments affecting hearing or vision.

Arms & Interventions

Virtual Reality Based Relaxation Program

Experimental

Virtual Reality Based Relaxation Program

Intervention: Virtual Reality Based Relaxation Program (Other)

Control group

No Intervention

Routine maintenance will be applied.

Outcomes

Primary Outcomes

Physiological Symptoms of Anxiety Follow-up Form

Time Frame: 1 hours later

This form was created by the researcher to record blood pressure, heart rate, respiratory rate and peripheral oxygen saturation value.

Visual Analog Scale

Time Frame: 1 hours later

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

Anxiety Assessment Scale

Time Frame: 1 hours later

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Gülcan Bahçecioğlu Turan

Principal Investigator

Ataturk University

Study Sites (1)

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