Effect of Virtual Reality Glasses on Pain, Anxiety, and Comfort During Extracorporeal Shock Wave Lithotripsy

NCT ID: NCT06804928

Last Updated: 2025-12-01

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

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-01

Study Completion Date

2025-10-10

Brief Summary

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Effect of Virtual Reality Glasses on Pain, Anxiety, and Comfort During ESWL

Detailed Description

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Conditions

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ESWL Anxiety Pain Comfort Virtual Reality

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Investigators Outcome Assessors
The measurements will be conducted by an individual independent of the study. Additionally, the statistical analysis of the research will be performed by a statistician who is unaware of the study details. The randomization plan was also prepared by a researcher independent of the study.

Study Groups

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VR-G (Virtual Reality Group) (1)

During the procedure, the patient will wear virtual reality glasses and watch a video. The video will be played through the virtual reality glasses throughout the entire procedure.

Group Type EXPERIMENTAL

Virtual Reality Glasses

Intervention Type BEHAVIORAL

During the procedure, the patient will wear virtual reality glasses and watch a video. The video will be played through the virtual reality glasses throughout the entire procedure.

Control Group (2)

No intervention will be applied to the patients in the control group, and the standard care protocol of the clinic will be followed.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Virtual Reality Glasses

During the procedure, the patient will wear virtual reality glasses and watch a video. The video will be played through the virtual reality glasses throughout the entire procedure.

Intervention Type BEHAVIORAL

Other Intervention Names

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Control group

Eligibility Criteria

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Inclusion Criteria

Being 18 years of age or older, Having no hearing or perception impairments, Having no visual impairments, Undergoing ESWL for the first time.

Exclusion Criteria

Use of any analgesic or anxiolytic medication before the procedure, Having a psychiatric disorder, The procedure being performed on an emergency basis.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Akdeniz University

OTHER

Sponsor Role lead

Responsible Party

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Seda Cansu Yeniğün

Lecturer Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Samsun Gazi State Hospital

Samsun, Merkez, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Scansuscansu92

Identifier Type: -

Identifier Source: org_study_id

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