Effect of GenAI Patient Simulation on Clinical Preparedness and Clinical Competence in Nursing Students
Effectiveness of Generative Artificial Intelligence (GenAI) Patient Simulation on Preparedness for Clinical Practicum and Clinical Competence Among Undergraduate Nursing Students: A Waitlist Randomized Controlled Trial and Mixed-methods Study
1 other identifier
interventional
44
0 countries
N/A
Brief Summary
The transition from theoretical knowledge to clinical practice is a critical and challenging phase for nursing students. Limited opportunities for scenario-based learning before an clinical practicum impacts students' preparedness for practice and clinical competence. Consequently, this lack of preparation directly fuels stress, creating a a negative feedback loop where this stress inhibits cognitive processing and effective learning. Generative artificial intelligence (GenAI) has emerged as a novel educational technology capable of providing interactive, flexible, and learner-centred simulation experiences. This waitlist randomised controlled trial aims to examine the effectiveness of incorporating the GenAI patient simulation in preparing the undergraduate nursing students for clinical practicum and enhancing the clinical competence compared to the current practice. Hypotheses of this study include:
- 1.Participants using the GenAI patient simulation will report higher preparedness for the first acute clinical practicum (CP) and higher clinical competence scores compared to the usual practice group at all time points.
- 2.The frequency of using the GenAI patient simulation will be positively correlated with preparedness for the CP and clinical competence.
- 3.Participants using the GenAI patient simulation will report lower perceived stress before and during the CP compared to the usual practice group.
- 4.The frequency of using of the GenAI patient simulation will negatively correlate with the levels of perceived stress before and during the CP.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Sep 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 3, 2026
CompletedFirst Posted
Study publicly available on registry
September 10, 2026
CompletedStudy Start
First participant enrolled
September 28, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 31, 2028
September 21, 2026
September 1, 2026
11 months
September 3, 2026
September 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Preparedness for Clinical Practicum
Preparedness for clinical practicum will be measured using the Casey-Fink Readiness for Practice Survey, consists of 15 items in three domains: clinical problem solving (6 items), learning activities (5 items), and practice readiness (4 items). The minimum and maximum mean scores for each subscale are 1 and 4, respectively. A higher mean score indicates a higher level of agreement with each subscale.
Baseline (T0), immediate after Phase 1 (T1), 2 weeks prior to the clinical practicum (T2), and within 1 week after completion of the clinical practicum (T3)
Clinical Competence
Measured by the Clinical Competency Questionnaire, consists of 47 items divided into four domains: nursing professional behaviour, general performance, core nursing skills and advanced nursing skills. Total scores range from 47 to 235, with a higher score indicating a higher level of competence.
Baseline (T0), immediate after Phase 1 (T1), 2 weeks prior to the clinical practicum (T2), and within 1 week after completion of the clinical practicum (T3)
Secondary Outcomes (1)
Perceived Stress
Baseline (T0), immediate after Phase 1 (T1), 2 weeks prior to the clinical practicum (T2), and within 1 week after completion of the clinical practicum (T3)
Study Arms (2)
Arm 1
EXPERIMENTALArm 2
OTHERWaitlist control
Interventions
The intervention is a two-phase GenAI patient simulation platform. Phase 1 - a 2-hour facilitated face-to-face simulation exercise session using the scenarios in the GenAI platform. Phase 2 - a self-initiated, wall-free GenAI patient simulation scenario package. Participants is allowed to access the platform and do the exercises before and during clinical practicum.
Eligibility Criteria
You may qualify if:
- Year 3 nursing students of a 5-year full-time Bachelor in Nursing programme,
- of any nationality including non-local and non-Chinese students, and
- able to read and understand English, and
- completed the introduction of clinical nursing practicum in year 2, and
- scheduled to undertake their first acute clinical practicum within the same academic year.
You may not qualify if:
- Year 3 nursing students of a 5-year full-time Bachelor in Nursing programme, who will not have their first acute clinical practicum within that academic year.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Miss
Study Record Dates
First Submitted
September 3, 2026
First Posted
September 10, 2026
Study Start
September 28, 2026
Primary Completion (Estimated)
August 31, 2027
Study Completion (Estimated)
March 31, 2028
Last Updated
September 21, 2026
Record last verified: 2026-09