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Not yet recruiting NCT07564544

AI-Based Clinical Orientation for Nursing Students

No phase Interventional Orientation Clinical

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Artificial Intelligence-Based Clinical Orientation Program.
Who it may be relevant to
Registry conditions: Orientation, Clinical. Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effects of an Artificial Intelligence-Based Clinical Orientation Program on Nursing Students Orientation Process in Pediatric Nursing Practice

Overview

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.

Interventions

  • Other Artificial Intelligence-Based Clinical Orientation Program
    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 aft

Primary outcome measures

  • Introductory Information Form [Time frame: 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 outcome measures (1)
  • Clinical Adaptation Scale for Student Nurses [Time frame: 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).]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

  • Being absent during the course of the study.
  • Currently being employed as a healthcare professional.
  • Having a frozen enrollment status.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Turkey (Türkiye) · 2 centers
  • Selcuk University — Konya
  • Selcuk University — Konya

Identifiers

NCT: NCT07564544 · SU-Clinic Orient

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗