Virtual Reality Application for Pain and Anxiety Reduction During Cystoscopy

NCT ID: NCT06079814

Last Updated: 2024-03-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-10

Study Completion Date

2024-12-10

Brief Summary

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The aim of this research is to conduct a two-group randomized controlled intervention study to determine the effect of virtual reality applications on pain and anxiety during cystoscopy. The study population will consist of patients who have applied to the urology outpatient clinic of a University Hospital for cystoscopy. The study sample will be composed of patients who volunteer to participate in the study and meet the criteria during the planned dates of the research. Data will be collected using a 'Personal Information Form' created by the researcher through a literature review, the 'Visual Analog Scale' (VAS) for assessing pain, and the 'State Anxiety Inventory' (SAI) for assessing anxiety.

Detailed Description

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Conditions

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Pain Anxiety

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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experiment group

Patients will wear virtual reality glasses 10 minutes before cystoscopy. The content chosen by the patient (there will be three options) will be watched throughout the procedure.

Group Type EXPERIMENTAL

virtual reality intervention

Intervention Type OTHER

Patients will be shown content through the patient's virtual reality glasses throughout the cystoscopy procedure.

control group

Standard procedure.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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virtual reality intervention

Patients will be shown content through the patient's virtual reality glasses throughout the cystoscopy procedure.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being literate,
* Being conscious,
* Ability to understand and speak Turkish and not have hearing or visual impairment,
* Agreeing to participate in the research.

Exclusion Criteria

* Having a diagnosed psychiatric and mental illness,
* Patients diagnosed with epilepsy (due to the risk of virtual reality glasses triggering epileptic seizures),
* Patients who do not want to continue the study
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cukurova University

OTHER

Sponsor Role lead

Responsible Party

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Seyma Yurtseven

Clinic Nurse

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Cukurova University

Adana, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Facility Contacts

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Sevban Arslan

Role: primary

05326938898

Other Identifiers

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5312256929

Identifier Type: -

Identifier Source: org_study_id

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