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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05814679
Other study ID # E1-22-3047
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 31, 2023
Est. completion date August 31, 2023

Study information

Verified date February 2024
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date August 31, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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 - Death

Study Design


Intervention

Other:
Relaxation with virtual reality
In this research, a virtual reality relaxation video will be used in which the natural wonders are presented to the audience in an immersive environment.
Attention match
kidney function instruction

Locations

Country Name City State
Turkey Ankara Cit Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fatigue Severity Scale In the study, fatigue symptom will be measured with the fatigue severity scale. 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.
Primary Hemodialysis Comfort Scale In the study, hemodialysis comfort will be measured with the hemodialysis comfort scale. 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.
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