- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07540078
Leveraging Large Language Models (LLM) to Enhance Research Competency Among Undergraduate Nursing Students: A Novel Approach to Research Education (NRAC)
The goal of this mixed method interventional study is to develop and test the effectiveness of integrating ChatGPT into the nursing research course to improve research competency among third-year undergraduate nursing students. The main questions it aims to answer is:
Will participants who undergo the LLM-integrated curriculum show an increase in research competency and attitudes compared to participants who did not undergo this curriculum.
Researchers will compare a students assessment grades, as well as their research competency and attitude, measured via the Research Competence Scale (R-Comp) and Revised Attitudes Towards Research scale (R-ATR) respectively. Research will determine whether the LLM-integrated curriculum could improve students understanding and attitudes towards research.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Singapore, Singapore
- National University of Singapore, Yong Loo Lin School of Medicine, Singapore, Singapore 117599
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All year-three students in cohort years AY2025/26 and AY2026/27 who are enrolled in mandatory research course titled "NUR3202C: Research and Evidence-Based Healthcare"
Exclusion Criteria:
- NIL
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: AY2025/2026 cohort
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|
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Experimental: AY2026/2027 cohort
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The curriculum for AY2026/2027 will have the following integrated into their lessons/ learning materials:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Research Competence questionnaire
Time Frame: Once at baseline (week 0), once at Week 10
|
A 32-item, 5-point Likert scale assessing participants perceived research competency.
The minimum and maximum score one can attain on this measure is 32 and 160 respectively, with a higher score indicating higher perceived competence in research
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Once at baseline (week 0), once at Week 10
|
|
Revised Attitudes Toward Research scale
Time Frame: Once at baseline (week 0), once at Week 10
|
A 13-item, 7-point Likert scale assessing participants' own attitudes towards research.
The minimum and maximum score one can attain on this measure is 13 and 91 respectively, with a higher score indicating a more positive attitude towards research.
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Once at baseline (week 0), once at Week 10
|
|
Grades of research proposal
Time Frame: Week 15
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Grades from the research proposal will also be used as an objective measure of the student's research competency for triangulation of data. This research proposal is an existing assessment in NUR3202C it will be assessed using a structured rubric that grades students based on the content, organization, delivery and collaboration. |
Week 15
|
Collaborators and Investigators
Collaborators
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 (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
- NUS-IRB-2025-136
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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