Natural Virtual Reality in the Application of Hospice Care

August 14, 2022 updated by: Far Eastern Memorial Hospital

In recent years, the use of Virtual Reality devices or somatosensory technology in various fields of teaching or sports has gradually matured. It is even possible to see that libraries or museums use virtual reality to promote reading or art. The trend of cross-border application has been born. The use of horticultural therapy in the current service of dementia or hospice patients is more common than in the past. The research team of the Taiwan Normal University has developed the first 3D Virtual Reality horticultural therapy course in Taiwan. Therefore, this study attempts to use natural virtual reality as an auxiliary care method to see if it can relieve the pain of hospitalized patients in the hospice ward, or relieve the stress of the caregiver (such as the patient's family or ward medical staff)!

The purpose of the study is:

  1. Use natural virtual reality as an auxiliary care mode to relieve the painful condition of inpatients in the hospice ward.
  2. Use natural virtual reality to relieve the psychological pressure of caregivers (family, medical colleagues).

The subjects of the study were: inpatients in the hospice ward of the hospital, caregivers of inpatients in the hospice ward, and medical staff of the hospice team.

Research methods:

  1. Use virtual reality head-mounted equipment to watch the natural landscape for 10 minutes each time. The patient and caregiver watched three times a week during hospitalization. The medical staff watched eight times a day on weekdays.
  2. Questionnaire: The patient used the pain scale and the Distress Thermometer (DT) scale as the pre-test questionnaire. The caregiver and the medical staff use the DT scale and the "Profile of Mood States (POMS)" as the pre-test questionnaire.

Expected results: The patient is expected to reduce the pain and enhance the quality of life by viewing the virtual natural landscape. It is expected that caregivers and medical colleagues can relieve stress and enhance the quality of life by watching virtual natural landscapes.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

120

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 Contact

Study Locations

    • Banciao Dist
      • New Taipei City, Banciao Dist, Taiwan, 220
        • Recruiting
        • Far Eastern Memorial Hospital
        • Contact:
          • Shin-Yi Lin

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

*Target: Inpatients in hospice Ward, carers of inpatients in hospice Ward, nurses or physicians of hospice team.

Exclusion Criteria:

  • Due to the use of virtual reality headsets, people with eye diseases (glaucoma or cataracts and other people who are sensitive to light) and people with a history of mental illness are excluded.
  • Inpatients in the hospice Ward also excluded those with tumors or diseases above the neck, those with symptoms of delirium, confusion, and unconsciousness.

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: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Inpatients in hospice Ward
Inpatients in hospice Ward with pain control problems
This study will use pain scale, distress thermometer and POMS to understand whether the patient's pain status have changed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain scale
Time Frame: up to 2 weeks
A single question, divided into 0-10 pain assessment scale.
up to 2 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Distress Thermometer, DT
Time Frame: up to 2 weeks
A single question, the height of emotional stress ranges from 0-10.
up to 2 weeks

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
POMS
Time Frame: up to 2 weeks
The scale is divided into seven factors: vitality, self-esteem, confusion, fatigue, anger, tension and tension, with 37 items in total.
up to 2 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Shin-Yi Lin, Family Medicine department

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)

November 7, 2019

Primary Completion (Actual)

November 7, 2019

Study Completion (Anticipated)

September 30, 2024

Study Registration Dates

First Submitted

August 11, 2020

First Submitted That Met QC Criteria

August 19, 2020

First Posted (Actual)

August 21, 2020

Study Record Updates

Last Update Posted (Actual)

August 16, 2022

Last Update Submitted That Met QC Criteria

August 14, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 108110-F

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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.

Clinical Trials on Natural Virtual Reality in the Application of Hospice Care

Clinical Trials on to relieve the pain of inpatients in the hospice Ward

3
Subscribe