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The Effect of Artificial Intelligence-assisted Visual Case Analysis on Nursing Students' Knowledge and Attitudes Towards Pressure Injury Prevention: A Single-blind Randomized Controlled Trial

NCT06978283 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2025-05-18

No results posted yet for this study

Summary

The goal of this clinical trial is to examine the effect of artificial intelligence-assisted visual case analysis on nursing students' knowledge and attitudes towards pressure injury prevention. The main hypotheses it aims to answer are:

* AI-assisted visual case analysis affects nursing students' knowledge about pressure injury prevention.
* AI-assisted visual case analysis affects nursing students' attitudes toward pressure injury prevention.

Researchers will compare AI-assisted case analysis to conventional case analysis to see if it affected nursing students' knowledge and attitudes about pressure injury prevention.

Participants,

* The case group will shown an AI-supported presentation explaining the pressure injury prevention case. The control group will given a classic case analysis.
* At the end of the case, the PUPKAI and APuP scales will administered to the students in written form in the classroom.

Conditions

  • Artificial Intelligence (AI)
  • Visual Case Analysis
  • Nursing Students
  • Pressure Injury Prevention
  • A Single-blind Randomized Controlled Trial

Interventions

BEHAVIORAL

AI-assisted case analysis

Nursing students will perform visual case analyses of pressure injuries using an AI-based platform. The AI system will provide students with case-based feedback.

BEHAVIORAL

Traditional case analysis

Participants will be present with written case scenarios and a case analysis will conduct with the instructor. The training process will be carried out with group discussions and the instructor's guidance. No technological or artificial intelligence support will be used.

Sponsors & Collaborators

  • Çankırı Karatekin University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-05-09
Primary Completion
2025-05-09
Completion
2025-07-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06978283 on ClinicalTrials.gov