Virtual Reality Glasses in Palliative Care

December 19, 2023 updated by: Yadigar Ordu, Necmettin Erbakan University

The Effect of Virtual Reality Glasses on the Psychological Well-Being and Care Burden of Patient Relatives Giving Care to Patients in the Palliative Care Clinic

Developments in medicine and technology have led to an increase in life expectancy and an increase in the need for palliative care. palliative Care aims to reduce or eliminate a life-threatening situation. The palliative care team cares for the patient and provides informal support to the patient. It should provide care that centers on caregivers (patient's relatives). Relatives of patients who provide palliative care are responsible for their care As it increases, problems such as fatigue, hopelessness and anger may occur. Problems experienced by caregivers of patients Eliminating this problem and integrating it into care by providing psychosocial support is essential for the quality of care. caregivers Health technologies can be used to support In our research, we found that virtual reality glasses were used in palliative care clinics. It is aimed to investigate the effect of patient relatives who care for inpatients on the psychological well-being and care burden. A randomized controlled research design was used in the study. The population of the research is a country in Turkey between June and October 2023. The study consisted of patient relatives who provide care to patients in the palliative care clinic of the public hospital in the province. To research Relatives of patients who met the participation criteria and agreed to participate (control group, n=22; experimental group, n=22) constituted the sample. Data were collected from "Caregiver Introduction Form", "Psychological Well-Being Scale", "Caregiving Burden Scale" and "Virtual Reality Glasses". It was collected using the "Satisfaction Form". Before starting the research, a preliminary study was conducted with four patient relatives. of research In the implementation, firstly the preliminary application of the data collection tools was made. Then, the experimental group was given weekly Videos containing 360-degree images were watched using virtual reality glasses for 30 minutes for three days. In the control group No intervention was made. At the end of the research, the final application of the data collection tools was made. From research The data obtained was analyzed with the SPSS 22.0 package program.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

44

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Konya, Turkey
        • Necmettin Erbakan University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Volunteering to participate in the research,
  • No vision, hearing or perception impairment that prevents communication,
  • Not using glasses to wear VR glasses,
  • No psychiatric disease,
  • Absence of complaints such as migraine, vertigo, active nausea, vomiting, headache,
  • Not having someone to help you care for your patient.

Exclusion Criteria:

  • Wanting to leave the research.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
No intervention was made to the control group. The posttest was administered four weeks after the pretest.As a result, caregivers' care burden and psychological well-being will be measured.
Experimental: Virtual Reality Group
A pretest was administered to the experimental group. Then, 360-degree VR videos (nature walks, trips, etc.) were watched three days a week for four weeks. Then, the final test was administered.As a result, caregivers' care burden and psychological well-being will be measured.
Using virtual reality glasses, caregivers in the experimental group were shown 360-degree VR relaxing videos.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
psychological well-being
Time Frame: Four weeks after pretest

The psychological well-being levels of caregivers will be evaluated using the psychological well-being scale.Psychological well-being scale (PIOS):

It was developed by Diener et al. in 2009 and consists of eight items. The scale measuring socio-psychological well-being is a single-factor and 7-point Likert type (1 = Strongly disagree, 7 = Strongly agree). The lowest score that can be obtained from the scale is 8 and the highest score is 56. A high score from the scale indicates high psychological well-being.

Four weeks after pretest

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Determine maintenance burden
Time Frame: Four weeks after pretest

Using the caregiving burden scale, caregivers' caregiving burden will be measured.

Caregiving burden scale:

The scale, developed by Zarit et al. in 1980 and adapted into Turkish by İnci and Erdem (2008), consists of 22 statements that determine the impact of caregiving on the individual's life. Scale items are generally related to the social and emotional domain and are of 4-point Likert type (0 = Never, 4 = Almost always). The lowest score that can be obtained from the scale is 0 and the highest score is 88. A high scale score indicates that the distress experienced is high (0-20 points = no care burden, 21-40 points = light care burden, 41-60 points = moderate care burden, 61-88 points = heavy care burden).

Four weeks after pretest

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 15, 2023

Primary Completion (Actual)

October 5, 2023

Study Completion (Actual)

October 15, 2023

Study Registration Dates

First Submitted

November 27, 2023

First Submitted That Met QC Criteria

November 27, 2023

First Posted (Actual)

December 5, 2023

Study Record Updates

Last Update Posted (Actual)

December 26, 2023

Last Update Submitted That Met QC Criteria

December 19, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • TUSEB (Other Identifier: Health Institutes of Türkiye)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Data may be requested from the principal investigator upon reasonable request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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