- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07172633
- Original Trial
Effects of Dementia Scenario-Based Simulation Teaching Combined With Virtual Technology Among Nursing Students
Effects of Scenario-Based Simulation Teaching Combined With Virtual Technology on Knowledge, Empathy, and Communication and Assessment Skills in Dementia Care Among Nursing Students
Study Overview
Status
Conditions
Detailed Description
This two-group randomised controlled trial aims to evaluate the effects of scenario-based simulation teaching with virtual technology on dementia knowledge, empathy, communication, and assessment skills among nursing students.
The interventional group will receive the 5-week scenario-based simulation teaching with a virtual coach in addition to regular dementia care lectures.
The control group will receive the 5-week traditional dementia case discussions in addition to regular dementia care lectures.
Both groups will be assessed for their dementia knowledge, empathy, communication, and assessment skills at baseline, week 12, and week 18.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Huei-Chuan Sung, PhD
- Phone Number: 22213 886-3-8572158
- Email: sung@gms.tcu.edu.tw
Study Locations
-
-
Hualien
-
Hualien City, Hualien, Taiwan, 970
- Recruiting
- Tzu Chi University
-
Contact:
- HUEICHUAN SUNG, PhD
- Phone Number: 22213 886-3-8572158
- Email: sung@gms.tcu.edu.tw
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- college nursing students with ages ranging from 18 to 40 years,
- Taiwanese nationality,
- provide informed consent to participate in the study.
Exclusion Criteria:
- college nursing students who do not meet the inclusion criteria
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Scenario-based simulation teaching with virtual technology
5-week scenario-based simulation teaching with a virtual coach intervention in addition to regular dementia care lectures
|
5-week scenario-based simulation teaching with a virtual coach acting as an older adult with dementia in addition to regular dementia care lectures
|
|
Active Comparator: traditional dementia case discussions
5-week traditional dementia case discussions in addition to regular dementia care lectures
|
5-week traditional dementia case discussions in addition to regular dementia care lectures
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dementia Knowledge Assessment Scale
Time Frame: baseline, week 12, week 18
|
Dementia Knowledge
|
baseline, week 12, week 18
|
|
Jefferson Scale of Empathy
Time Frame: baseine, week 12, week 18
|
empathy
|
baseine, week 12, week 18
|
|
Nursing Students' Communication Behavior with Dementia Patients Scale
Time Frame: baseine, week 12, week 18
|
Communication behavior with dementia patients
|
baseine, week 12, week 18
|
|
Health Professionals Communication Skills Scale
Time Frame: baseline, week 12, week 18
|
communication skills
|
baseline, week 12, week 18
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dementia Assessment Practice Rubrics
Time Frame: baseline, week 12, week 18
|
assessment skills for people with dementia
|
baseline, week 12, week 18
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PMN1141602
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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