The Effect of Virtual Reality Application on Pain Due to Fistula Puncture in Hemodialysis Patients
NCT ID: NCT05807906
Last Updated: 2024-02-28
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
14 participants
INTERVENTIONAL
2023-04-17
2023-05-31
Brief Summary
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Hypotheses of the Research:
H0-1: Virtual reality application has an effect on fistula puncture-related pain in HD patients.
H1-2: Virtual reality application has no effect on fistula puncture-related pain in HD patients.
In the study, virtual reality will be applied in the fistula puncture procedure in patients receiving hemodialysis treatment.
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Detailed Description
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* The patient will be prepared for the virtual reality application and fistula puncture and will be given a comfortable sitting position.
* Virtual reality glasses will be put on the patient 6 minutes before the fistula puncture and the application will be started.
* The patient will continue to monitor the virtual reality application during the fistula puncture procedure. It will be ensured that no communication with the patient is made until the application is finished.
* The application will be ended with the fixation of the needle on the fistula after the fistula puncture procedure.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
TRIPLE
Study Groups
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Intervention Group
virtual reality will be applied in the fistula puncture procedure in patients receiving hemodialysis treatment.
virtual reality application
The patient will continue to monitor the virtual reality application during the fistula puncture procedure.
Control Group
Routine nursing care and diet compliance narration
No interventions assigned to this group
Interventions
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virtual reality application
The patient will continue to monitor the virtual reality application during the fistula puncture procedure.
Eligibility Criteria
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Inclusion Criteria
* No sedatives, analgesics and sedatives are applied 3 hours before the application.
* Not taking recently taken antipsychotic drugs and tranquilizers,
* Deaf and visually impaired (to mark VAS pain)
* Without cognitive and psychiatric diagnosis
* Open to communication and cooperation
* Patients who agreed to participate in the study
Exclusion Criteria
* Discomfort due to virtual reality glasses
* Suspected/diagnosed COVID-19
* Patients who want to leave the study voluntarily
* Death
* Multiple fistula puncture attempts
18 Years
65 Years
ALL
No
Sponsors
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Hacettepe University
OTHER
Responsible Party
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Neşe Altinok Ersoy
Principal Investigator
Locations
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Ankara City Hospital
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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E1-22-2882
Identifier Type: -
Identifier Source: org_study_id
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