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Clinical Trials/NCT05814679
NCT05814679
Completed
Not Applicable

The Effect of Relaxation With Virtual Reality on Fatigue and Comfort in Hemodialysis Patients

Hacettepe University1 site in 1 country12 target enrollmentMay 31, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Kidney Diseases
Sponsor
Hacettepe University
Enrollment
12
Locations
1
Primary Endpoint
Fatigue Severity Scale
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Based on the task of providing the comfort of the patient, which is an indispensable part of the nursing profession, which many nurse theorists emphasize, there has been no study in the literature on the determination of the effect of virtual relaxation, which can be effective on the fatigue and comfort levels of patients receiving hemodialysis treatment. Therefore, the aim of this study is to examine the effect of virtual reality and relaxation on fatigue and comfort in hemodialysis patients.

Detailed Description

The patient will be prepared for relaxation with virtual reality and will be given a comfortable sitting position. The patient will watch the relaxation practice with virtual reality once during the hemodialysis treatment. The application will be terminated with the expiration of the virtual reality relaxation video. Fatigue and comfort score will be measured after the application.

Registry
clinicaltrials.gov
Start Date
May 31, 2023
End Date
August 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Neşe Altinok Ersoy

Research Assistant (pHD)

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • Receiving hemodialysis treatment for the last 6 months
  • Receiving four-hour hemodialysis treatment three times a week
  • 18 years or older
  • Deaf and visually impaired
  • Without cognitive and psychiatric diagnosis
  • Open to communication and cooperation
  • Patients who agreed to participate in the study

Exclusion Criteria

  • Kidney transplant
  • Discomfort due to virtual reality glasses
  • Suspected/diagnosed COVID-19
  • Patients who want to leave the study voluntarily

Outcomes

Primary Outcomes

Fatigue Severity Scale

Time Frame: Assessing change of fatigue severity scale scores baseline, after each application for three weeks. Between third and fifth weeks any intervention will not be implemented and fatigue severity scale score will measure fifth week.

In the study, fatigue symptom will be measured with the fatigue severity scale.

Hemodialysis Comfort Scale

Time Frame: Assessing change of fatigue comfort scale scores baseline, after each application for three weeks. Between third and fifth weeks any intervention will not be implemented and comfort scale score will measure fifth week.

In the study, hemodialysis comfort will be measured with the hemodialysis comfort scale.

Study Sites (1)

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