- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04788992
Dementia Care Training With Virtual Reality and Support for Home Care Staff
Evaluation of a Dementia Care Training With Virtual Reality and Support Program for Home Care Staff
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Home care staff often have insufficient knowledge and skills of caring people with dementia at home. Many lack empathy for those with dementia. Training courses for home care staff often are not developed according to their educational background and workplace needs.
This two-group cluster randomised controlled trial aims to evaluate a dementia care training with virtual reality and peer support program on dementia care knowledge, attitude, care competence, work stress, and empathy of home care staff.
The dementia care training consists of dementia care e-books, dementia virtual reality activity and peer support program.
The interventional group will receive a dementia care training using dementia care e-books, dementia virtual reality activity and peer support program.
The control group will only receive dementia care e-books and peer support with no dementia virtual reality activity.
Both groups will be assessed for their dementia care knowledge, attitudes, care competence, work stress and empathy at baseline, month 3, and 6.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Hualien City, Taiwan, 970
- Mennonite Social Welfare foundation
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age 20 to 65 years
- Taiwanese nationality
- had worked as a home care staff for at least three months
- had experience in providing home care for patients with dementia
- had a mobile phone or tablet and regular access to the internet
Exclusion Criteria:
- Home care staff who do not meet the inclusion criteria
- can not provide informed consent.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
receive dementia care training
|
Dementia care training consists of dementia care e-books, dementia virtual reality activity and peer support program.
|
|
Active Comparator: Control group
receive dementia care training without virtual reality activity
|
Dementia care training consists of dementia care e-books and peer support program without dementia virtual reality activity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dementia Knowledge Assessment Scale
Time Frame: 6 months
|
To evaluate care staff's knowledge of dementia, range from 0-50
|
6 months
|
|
Approach to Dementia Questionnaire
Time Frame: 6 moths
|
To evaluate care staff's attitude toward Dementia, range from 19-95
|
6 moths
|
|
Sense of Competence in Dementia Care Staff Scale
Time Frame: 6 months
|
To evaluate care staff's competence of caring for people with dementia, range from 16-68
|
6 months
|
|
Jefferson Scale of Empathy
Time Frame: 6 months
|
To evaluate care staff's level of empathy toward patients, score range from 20-140
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Simple Work Stress Scale
Time Frame: 6 moths
|
To evaluate level of work stress of care staff
|
6 moths
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Huei-Chuan Sung, PhD, Tzu Chi University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- YLH-IRB-10815
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
product manufactured in and exported from the U.S.
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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