Virtual Reality Glasses in Palliative Care

Virtual Reality Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06156540
• Other study ID #: TUSEB
• Status: Completed
• Phase: N/A
• Start date: June 15, 2023
• Est. completion date: October 15, 2023

Study information

• Verified date: December 2023
• Source: Necmettin Erbakan University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: October 15, 2023
• Est. primary completion date: October 5, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

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.

Related Conditions & MeSH terms

• Virtual Reality

Intervention

Other:
• virtual reality glasses
Using virtual reality glasses, caregivers in the experimental group were shown 360-degree VR relaxing videos.

Locations

Country	Name	City	State
Turkey	Necmettin Erbakan University	Konya

Sponsors (2)

Lead Sponsor	Collaborator
Necmettin Erbakan University	Health Institutes of Turkey

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	psychological well-being	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	Determine maintenance burden	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 Inci 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