AI-Based Clinical Orientation for Nursing Students
ClinicOrient
The Effects of an Artificial Intelligence-Based Clinical Orientation Program on Nursing Students Orientation Process in Pediatric Nursing Practice
1 other identifier
interventional
90
1 country
2
Brief Summary
Aim: This experimental study aims to investigate the impact of an Artificial Intelligence (AI)-based orientation program on the clinical orientation process of nursing students during their pediatric nursing clinical practice.Materials and Methods: The study population will consist of 186 third-year nursing students enrolled in the spring semester at a state university. The sample will include 90 students (45 intervention, 45 control) who meet the study criteria and volunteer to participate. Students in the intervention group will receive an AI-based clinical orientation program, while the control group will receive no additional intervention beyond the standard faculty and hospital orientation. Data will be collected between February and March 2026 using a "Descriptive Information Form," the "Clinical Adaptation Scale for Student Nurses," and the "Therapeutic Communication Skills Scale for Nursing Students" in a pre-test/post-test design.Statistical Analysis: Data will be analyzed using SPSS 25.0. Descriptive statistics (frequency, percentage, mean, and standard deviation) will be used. Normality will be assessed via Kolmogorov-Smirnov/Shapiro-Wilk tests. For group comparisons, Chi-square, ANOVA, independent samples t-test, Mann-Whitney U, and Wilcoxon tests will be utilized. The statistical significance level will be set at $p \< 0.05$.Ethical Considerations: Ethical committee approval and necessary permissions from scale authors will be obtained before the study begins. Informed consent will be collected from all participants after explaining the study objectives.Keywords: Orientation training, nursing, student, artificial intelligence, clinical practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
2 active sites
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
April 16, 2026
CompletedStudy Start
First participant enrolled
April 30, 2026
CompletedFirst Posted
Study publicly available on registry
May 4, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 11, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 11, 2026
May 4, 2026
April 1, 2026
11 days
April 16, 2026
April 26, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Introductory Information Form
The form was developed by the researchers in line with the relevant literature (Günerigök et al., 2020; Yılmaz et al., 2021; Demiray \& İlaslan, 2021; Saydamlı et al., 2025; Baysan Arabacı et al., 2014). The form consists of 3 sections and 8 questions: descriptive characteristics (age, gender, grade point average), information related to clinical adaptation (difficulty in adapting when first starting the clinical environment, difficulty in communicating with patients/families during clinical practice, and experiencing anxiety-stress before clinical practice), and information related to artificial intelligence (use of artificial intelligence programs and willingness to learn and use technological developments such as artificial intelligence).
Pre-test (before the AI-supported orientation training), post-test (2 weeks after the AI-supported orientation training), and follow-up test (2 months later).
Secondary Outcomes (1)
Clinical Adaptation Scale for Student Nurses
Pre-test (before the AI-supported orientation training), post-test (2 weeks after the AI-supported orientation training), and follow-up test (2 months later).
Other Outcomes (1)
Therapeutic Communication Skills Scale for Nursing Students
Pre-test (before the AI-supported orientation training), post-test (2 weeks after the AI-supported orientation training), and follow-up test (2 months later).
Study Arms (2)
Control Group
NO INTERVENTIONStudents who do not receive AI-supported orientation training.
Intervention Group
EXPERIMENTALStudents receiving AI-supported orientation training
Interventions
The program was implemented via a researcher-developed website featuring seven modules: Therapeutic Communication, Patient Safety, Medical Equipment, Infection Control, Care Plans, Ethics/Privacy, and Stress Management. AI was utilized to develop scenarios, create audiovisual materials, and simulate realistic clinical environments. Each 5-minute video used no real patient data. A sequential progression was enforced, requiring completion of one module to start the next. Knowledge was assessed after each module via 5-10 Kahoot questions. A gamified approach was used where the fastest, most accurate students earned digital badges, with the top three overall being recognized as winners. Content validity was ensured through expert opinions from pediatric nursing faculty, and necessary adjustments were made based on their feedback.
Eligibility Criteria
You may qualify if:
- Being enrolled in the Pediatric Nursing course for the first time.
- Being a third-year nursing student.
- Providing voluntary informed consent to participate in the study.
You may not qualify if:
- Being absent during the course of the study.
- Currently being employed as a healthcare professional.
- Having a frozen enrollment status.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Selcuk University
Konya, Konya, 42250, Turkey (Türkiye)
Selcuk University
Konya, Selçuklu, 42060, Turkey (Türkiye)
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Fatma Tas Arslan
Selcuk University
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
- Professor
Study Record Dates
First Submitted
April 16, 2026
First Posted
May 4, 2026
Study Start
April 30, 2026
Primary Completion (Estimated)
May 11, 2026
Study Completion (Estimated)
June 11, 2026
Last Updated
May 4, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share