The Effect of Virtual Reality Glasses Application on Pain, Anxiety, and Patient Satisfaction
NCT ID: NCT05509114
Last Updated: 2022-08-19
Study Results
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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COMPLETED
NA
70 participants
INTERVENTIONAL
2021-12-25
2022-07-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Virtual Reality Glasses
The intervention introductory information formula was face-to-face by researchers from the State-Trait Anxiety Inventory (STAI-I, STAI-II), the Scale of Patient Perception of Hospital Experience with Nursing Care (PPHEN) and Visual Analog Scale for Pain (VAS) Before starting the research, a preliminary application plan is determined with 10 virtual virtual applications. It is not included in the applications made in the pre-application. Before watching the video, patients are informed about how to train, how to do it, and detailed information about the video. When the patient is removed from the service and in the left lateral position, 2 minutes before the assistant physician, the virtual is about to take place. The video was watched after about 10-15 minutes until the process was finished. After the procedure, STAI-I, STAI-II, PPHEN and VAS were reapplied by the researchers.
Virtual Reality Glasses
The intervention group of patients watched a video with virtual reality glasses during the transrectal biopsy process.
Interventions
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Virtual Reality Glasses
The intervention group of patients watched a video with virtual reality glasses during the transrectal biopsy process.
Eligibility Criteria
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Inclusion Criteria
* Those who volunteer and accept to participate in the research,
* Transrectal prostate biopsy procedure performed for the first time,
* No communication problem,
* Cognitive level scales are suitable for application,
* Patients without vision or hearing problems were included in the study.
Exclusion Criteria
* Patients whose cognitive level scales were not suitable for application were excluded from the study.
18 Years
65 Years
MALE
Yes
Sponsors
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Ataturk University
OTHER
Responsible Party
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Rumeysa Lale TORAMAN
Research Assistant
Principal Investigators
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Rumeysa Lale TORAMAN
Role: PRINCIPAL_INVESTIGATOR
Ataturk University
Locations
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Rumeysa Lale TORAMAN
Palandöken, Erzurum, Turkey (Türkiye)
Countries
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Other Identifiers
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Rumeysa
Identifier Type: -
Identifier Source: org_study_id
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