- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07275372
Using Virtual Humans to Teach Cognitive Function Assessment to Nursing Students (VHCT-NS)
Effectiveness of Virtual Humans in Learning Cognitive Function Assessment Among Nursing Students
Purpose of the Study This study wants to find out whether a virtual human (a computer-based simulated person) can help nursing students learn how to assess someone's thinking and memory skills.
Main Question Do nursing students learn cognitive function assessment better when they use a virtual human compared with reading printed materials?
What Participants Will Do Participants will learn how to do a cognitive function assessment for about 60 minutes, either by using a virtual human or by reading printed materials.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Chia-I Chao
- Phone Number: 886-930120686
- Email: b405112016@tmu.edu.tw
Study Locations
-
-
Taiwan
-
Taipei, Taiwan, Taiwan, 110
- Recruiting
- Taipei Medical University
-
Contact:
- Yeu-Hui Chuang, PhD
- Phone Number: 6328 886-2-27361661
- Email: yeuhui@tmu.edu.tw
-
Principal Investigator:
- Yeu-Hui Chuang, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Nursing students currently enrolled in a bachelor's or post-baccalaureate nursing program.
- Students who have not previously received instruction on the SPMSQ cognitive function assessment,
Exclusion Criteria:
- no
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: Virtual human
This group will use virtual human to learn the assessement of SPMSQ.
|
There are five scenarios integrated into Virtual human software.
|
|
Active Comparator: Printed material
The comparison group will use printed material to learn the assessment of SPMSQ.
|
The comparison group will read the printed material regarding SPMSQ assessment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Competence of cognitive function assessment
Time Frame: 60 minutes
|
Participants are required to conduct a cognitive function assessment on the virtual patient within a designed clinical scenario.
The system assigns a score based on the completion of each item, with higher scores indicating better cognitive assessment ability.
|
60 minutes
|
|
Knowledge of cognitive function assessment
Time Frame: 60 minutes
|
A total of ten items were included.
Each correct answer receives one point, while incorrect or "don't know" responses receive zero points.
The total score ranges from 0 to 10, with higher scores indicating better knowledge of cognitive function assessment among the students.
|
60 minutes
|
|
Confidence scale
Time Frame: 60 minutes
|
The scale consists of five items, each scored from 1 to 5, with a total score ranging from 5 to 25.
Higher scores indicate greater confidence in performing cognitive function assessments among the participants.
|
60 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Learning Material Satisfaction Questionnaire
Time Frame: 60 minutes
|
The questionnaire includes 10 items and is scored on a 5-point Likert scale, where "strongly disagree" = 1, "disagree" = 2, "neutral" = 3, "agree" = 4, and "strongly agree" = 5.
The total score ranges from 10 to 50, with higher scores indicating greater satisfaction with the learning material (either the VH-based material or the printed material).
|
60 minutes
|
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
Other Study ID Numbers
- N202510056
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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