- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06528925
Effect of Virtual Reality Goggles on Pain, Anxiety and Hemodynamic Variables During Urodynamics
July 17, 2025 updated by: Gamze BOZKUL, Tarsus University
Effect of Virtual Reality Goggles on Pain, Anxiety and Hemodynamic Variables During Urodynamics: A Randomized Controlled Study
The research was planned as a randomized controlled experimental study to determine the effect of virtual reality goggles on pain, anxiety and hemodynamic variables during urodynamics.
The minimum sample size was calculated as 42 in each group with d=0.8, (1- α, bidirectional), 95% power with reference to the effect size limit of 0.8 in G*Power (3.1) program.
Descriptive Information Form, Visual Analog Scale, State Anxiety Scale and Hemodynamic Variables Monitoring Form will be used to collect research data.
The individuals in the sample group will be informed about the method followed in the application and the research and their verbal and written permissions will be obtained.
Introductory Information Form, Visual Analog Scale, State Anxiety Scale and Hemodynamic Variables Monitoring Form will be completed.
After the forms are applied to the patients and recorded, it will be determined whether they will be in the study or control group according to the randomization schedule.Patients in the study group will be shown videos with virtual reality glasses during the procedure.
Nature landscapes with relaxing music background will be watched with virtual reality goggles by adjusting the volume at the level desired by the patient.
Virtual reality goggles will be applied during the urodynamic procedure.
The control group will receive routine care.
After the virtual reality application, pain, anxiety levels and hemodynamic variables will be re-evaluated immediately and 15 minutes after the procedure.
The data obtained in the study will be analyzed using SPSS (Statistical Package for Social Sciences) for Windows 25.0 program.
Descriptive statistical methods (number, percentage, min-max values, mean and standard deviation) will be used to evaluate the data.
Parametric and nonparametric tests will be used according to the suitability of the data used for normal distribution.
P < 0.05 will be taken as statistically significant difference
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The research was planned as a randomized controlled experimental study to determine the effect of virtual reality goggles on pain, anxiety and hemodynamic variables during urodynamics.
The population of the study, which is planned as a randomized controlled experimental study, will consist of patients who apply to the Urology Outpatient Clinic of Mersin University Hospital and will undergo urodynamics.
The minimum sample size was calculated as 42 in each group with d=0.8, (1- α, bidirectional), 95% power with reference to the effect size limit of 0.8 in G*Power (3.1) program.
Descriptive Information Form, Visual Analog Scale, State Anxiety Scale and Hemodynamic Variables Monitoring Form will be used to collect research data.
The individuals in the sample group will be informed about the method followed in the application and the research and their verbal and written permissions will be obtained.
Introductory Information Form, Visual Analog Scale, State Anxiety Scale and Hemodynamic Variables Monitoring Form will be completed.
After the forms are applied to the patients and recorded, it will be determined whether they will be in the study or control group according to the randomization schedule.Patients in the study group will be shown videos with virtual reality glasses during the procedure.
Nature landscapes with relaxing music background will be watched with virtual reality goggles by adjusting the volume at the level desired by the patient.
Virtual reality goggles will be applied during the urodynamic procedure.
The control group will receive routine care.
After the virtual reality application, pain, anxiety levels and hemodynamic variables will be re-evaluated immediately and 15 minutes after the procedure.
The data obtained in the study will be analyzed using SPSS (Statistical Package for Social Sciences) for Windows 25.0 program.
Pearson-χ2 test will be used for categorical variables.
Descriptive statistical methods (number, percentage, min-max values, mean and standard deviation) will be used to evaluate the data.
Parametric and nonparametric tests will be used according to the suitability of the data used for normal distribution.
P < 0.05 will be taken as statistically significant difference
Study Type
Interventional
Enrollment (Actual)
84
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Mersin, Turkey, 33400
- Mersin University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Who agreed to participate in the study,
- between the ages of 18-65
- Conscious, oriented and cooperative,
- No communication problems,
- undergoing invasive urodynamics,
- No physical problems that would prevent the application of virtual reality goggles,
- No previous experience with virtual reality glasses,
- Undiagnosed anxiety,
- No medication for anxiety
- Patients without mental disorders
Exclusion Criteria:
- Who did not agree to participate in the study,
- Under 18 or over 65 years of age,
- Conscious, oriented and uncooperative,
- Communication problems,
- No invasive urodynamics procedure,
- Physical problem that would prevent the application of virtual reality goggles,
- Diagnosed with anxiety,
- Taking medication for anxiety (anxiolytics, antidepressants, antipsychotics, etc.),
- Patients with mental disorders
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: EXPERIMENTAL GROUP
After the forms are applied to the patients and recorded, it will be determined whether they will be in the study or control group according to the randomization schedule.
Patients in the study group will be shown a video with virtual reality glasses during the procedure.
Patients will be asked to wear a virtual reality goggle (VR Box Virtual Reality Headset 3D Vr Glasses V2.0 2020 model) that is compatible with a mobile phone (Xiaomi Redmi Note 8 Pro 2019 model) with android operating system and minimizes sound loss in the supine position.
With the virtual reality glasses, nature landscapes with relaxing music background will be watched by adjusting the volume at the level desired by the patient.
Virtual reality glasses will be applied during the urodynamics procedure.
After the device is applied to each patient, it will be disinfected in accordance with the company's recommendation.
|
Patients in the study group will be shown a video with virtual reality glasses during the procedure.
Patients will be asked to wear a virtual reality goggle (VR Box Virtual Reality Headset 3D Vr Glasses V2.0 2020 model) that is compatible with a mobile phone (Xiaomi Redmi Note 8 Pro 2019 model) with android operating system and minimizes sound loss in the supine position.
With the virtual reality glasses, nature landscapes with relaxing music background will be watched by adjusting the volume at the level desired by the patient.
Virtual reality goggles will be applied during the urodynamic procedure.
|
|
No Intervention: CONTROL GROUP
The control group will receive routine care.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain score
Time Frame: 7 months
|
Visual Analog Scale: It is a scale that provides a subjective assessment of pain on a horizontal or vertical line from 0 (no pain at all)-10 (very severe pain) to evaluate the level of pain (Wewers and Lowe, 1990).
|
7 months
|
|
Anxiety
Time Frame: 7 months
|
The State Anxiety Scale : In this study, the DAQ, which is structured to measure momentary feelings, was used.
Its Turkish validity and reliability was conducted by Öner and Le Compte in 1983.
The DAQ consists of 20 questions on a four-point Likert scale.
The statements in the DAQ are evaluated as not at all (1), a little (2), a lot (3) and completely (4).
In this section, the statements are divided into direct and reversed statements.
Inverted statements: 1st, 2nd, 5th, 5th, 8th, 8th, 10th, 11th, 15th, 16th, 19th, 20th items.
The total score of the reversed statements is subtracted from the total score of the direct statements and the number 50, which is the invariant value of the DAQ, is added to the value obtained and the DAQ score is calculated.
The scale score ranges between 20-80 and an increase in the score indicates an increase in the level of anxiety.
|
7 months
|
|
Hemodynamic Variables
Time Frame: 7 months
|
Hemodynamic Variables Monitoring Form : In this form, hemodynamic variables of the study and control groups measured before, immediately after and 15 minutes after the procedure will be recorded.
Patient values will be measured and recorded by the investigator
|
7 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Gülay ALTUN UĞRAŞ, Mersin University
- Principal Investigator: Murat Bozlu, Mersin University
- Principal Investigator: Elife KETTAŞ DÖLEK, Mersin Unıversity Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Genc H, Korkmaz M, Akkurt A. The Effect of Virtual Reality Glasses and Stress Balls on Pain and Vital Findings During Transrectal Prostate Biopsy: A Randomized Controlled Trial. J Perianesth Nurs. 2022 Jun;37(3):344-350. doi: 10.1016/j.jopan.2021.09.006. Epub 2022 Apr 7.
- Biardeau X, Lam O, Ba V, Campeau L, Corcos J. Prospective evaluation of anxiety, pain, and embarrassment associated with cystoscopy and urodynamic testing in clinical practice. Can Urol Assoc J. 2017 Mar-Apr;11(3-4):104-110. doi: 10.5489/cuaj.4127.
- Dogan Yilmaz E, Unlusoy Dincer N. The Effects of Virtual Reality Glasses on Vital Signs and Anxiety in Patients Undergoing Colonoscopy: A Randomized Controlled Trial. Gastroenterol Nurs. 2023 Jul-Aug 01;46(4):318-328. doi: 10.1097/SGA.0000000000000733. Epub 2023 Jun 5.
- Drake MJ, Doumouchtsis SK, Hashim H, Gammie A. Fundamentals of urodynamic practice, based on International Continence Society good urodynamic practices recommendations. Neurourol Urodyn. 2018 Aug;37(S6):S50-S60. doi: 10.1002/nau.23773.
- Gammie A, Drake MJ. The fundamentals of uroflowmetry practice, based on International Continence Society good urodynamic practices recommendations. Neurourol Urodyn. 2018 Aug;37(S6):S44-S49. doi: 10.1002/nau.23777.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 15, 2024
Primary Completion (Actual)
January 15, 2025
Study Completion (Actual)
February 15, 2025
Study Registration Dates
First Submitted
July 24, 2024
First Submitted That Met QC Criteria
July 29, 2024
First Posted (Actual)
July 30, 2024
Study Record Updates
Last Update Posted (Actual)
July 22, 2025
Last Update Submitted That Met QC Criteria
July 17, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TU-BOZKUL-008
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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