- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06373172
Enhancing Clinical Reasoning Competency (Reasoning)
Enhancing Clinical Reasoning Competency for Undergraduate Nursing Students Using Virtual Simulation-based Education Based on the Rasch Model
Enhancing Clinical Reasoning Competency for Undergraduate Nursing Students Using Virtual Simulation-based Education based on the Rasch model
Aims: Clinical reasoning is a core nursing competency that involves analyzing patient-related data and providing appropriate nursing practices. Simulation-based education is effective in improving the clinical reasoning competencies and communication skills of nursing students. This study aimed to verify the effectiveness of virtual simulation-based education.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Methods: This study used a single-group pre- and post-test experimental design to verify the effectiveness of virtual simulation-based education. Data were collected from June to September 2020. Thirty-six nursing students in the 3rd and 4th grades who understood the purpose of this study were selected as participants. The collected data were analyzed using SPSS Statistics 25.0 and Winsteps 3.68.2.
Keywords: Clinical Reasoning, Competency, Communication, Nursing, Virtual Simulation
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Busan, Korea, Republic of, 48520
- Tongmyong Unoversity
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- The participants were third- and fourth-year undergraduate nursing students who understood the purpose of the study and voluntarily agreed to participate
Exclusion Criteria:
- A person who has difficulty communicating or has no willingness to participate
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Enhancing Clinical Reasoning Competency for Undergraduate Nursing Students
Enhancing Clinical Reasoning Competency for Undergraduate Nursing Students Using Virtual Simulation-based Education based on the Rasch model
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We used "vSim® for Nursing - Nursing Medical-Surgical" as the virtual simulation-based education program.
Four modules were included: (a) acute myocardial infarction, (b) diabetes mellitus, (c) transfusion, and (4) asthma.
Each module learning sessions was conducted based on scenarios, which consisted of five steps: Suggested reading, Pre-simulation quiz, vSim, Post-simulation quiz, and Guide reflection questions.
For each module, the intervention was performed for two hours.
The participants attended four module learning sessions and received eight hours of training.
Debriefing using guided reflection questions were completed in the form of a team reflection, followed by an instructor-learner discussion and feedback for 20 minutes of each module.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Nurses Clinical Reasoning Scale
Time Frame: 4month
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The Nurses Clinical Reasoning Scale (NCRS) includes 15 items rated on a five-point Likert scale (1=Strongly disagree, 5=Strongly agree, min:15 & max:75) (Liou et al., 2016).
We used the Korean version of the NCRS in this study (Joung & Han, 2017).
Higher scores indicated better clinical reasoning.
Cronbach's α was 0.94 for the original NCRS, and 0.93 for the Korean version of the NCRS.
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4month
|
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Communication Skills Scale
Time Frame: 4month
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The Global Interpersonal Communication Competence Scale (GICC-15) includes 15 items rated on a five-point Likert scale (1= strongly disagree to 5= strongly agree.
min:15 & max:75) (Rubin & Martin, 1994).
We used the Korean version of the GICC-15 (Hur, 2003).
Cronbach's α in Hur's (2003) study was 0.72.
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4month
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sung Hae Kim, PhD, Tongmyong 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
Other Study ID Numbers
- 202005-HR-003
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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