- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04522440
Natural Virtual Reality in the Application of Hospice Care
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:
- Use natural virtual reality as an auxiliary care mode to relieve the painful condition of inpatients in the hospice ward.
- 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:
- 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.
- 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
Status
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shin-Yi Lin
- Phone Number: +886 277284952
- Email: lanya2011@gmail.com
Study Locations
-
-
Banciao Dist
-
New Taipei City, Banciao Dist, Taiwan, 220
- Recruiting
- Far Eastern Memorial Hospital
-
Contact:
- Shin-Yi Lin
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Investigators
- Principal Investigator: Shin-Yi Lin, Family Medicine department
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 108110-F
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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