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AI-Supported E-Learning for Pressure Injury Prevention

16 de junio de 2026 actualizado por: İslam Elagöz, Kilis 7 Aralik University

The Effect of an AI-Supported Modular E-Learning Programme for Pressure Injury Prevention on Nursing Students' Knowledge, Attitudes and Self-Efficacy: A Randomised Controlled Trial

Brief Summary

Pressure injuries are damage to the skin and underlying tissue that may occur in patients who stay in bed for long periods, have limited mobility or use medical devices. These injuries are often preventable. They may cause pain, infection, longer hospital stays and increased care costs. For this reason, it is important that nurses and nursing students have accurate knowledge, confidence and positive attitudes about preventing pressure injuries.

The aim of this study is to compare two different methods of teaching pressure injury prevention to nursing students. One group of students received the education in a face-to-face classroom session. The other group completed the same topic through an artificial intelligence-supported modular e-learning programme. The e-learning programme included short videos, clinical examples, question-and-answer activities, short quizzes and feedback. The educational materials prepared with artificial intelligence support were checked by experts before being used with students.

Undergraduate nursing students took part in the study. The students were randomly assigned to one of two groups. In both groups, measurements were taken before the education, immediately after the education and four weeks later. The study assessed students' knowledge of pressure injury prevention, their confidence in managing pressure injury prevention and their attitudes towards prevention.

This study does not provide a treatment or direct intervention to patients. However, its findings may help improve how nursing students and future healthcare professionals are educated about pressure injury prevention. In the long term, better education may support safer patient care, help prevent pressure injuries and improve the quality of care.

Descripción general del estudio

Descripción detallada

Detailed Description

This study is a single-centre, two-arm, parallel-group randomised controlled educational trial comparing two different teaching methods for pressure injury prevention. The study was conducted with undergraduate nursing students in the nursing department of a faculty of health sciences.

Pressure injuries are an important patient safety problem, especially for patients with limited mobility, patients in intensive care, patients after surgery and patients using medical devices. Preventing pressure injuries requires regular risk assessment, skin inspection, appropriate positioning, pressure redistribution, nutritional assessment, monitoring of device-related pressure and continuity of care. Therefore, it is important that nursing students develop adequate knowledge, self-efficacy and positive attitudes before graduation.

In this study, students were randomly assigned to one of two groups. The first group received pressure injury prevention education through conventional face-to-face classroom instruction. The second group completed the same core content through an artificial intelligence-supported modular e-learning programme. Both educational methods covered key topics, including the causes of pressure injuries, classification, risk assessment, nutrition, preventive interventions, care for special patient groups and medical device-related pressure injuries.

The artificial intelligence-supported e-learning programme consisted of short video presentations, narration scripts, clinical examples, question-and-answer activities, short quizzes and feedback sections. The educational materials were prepared with the support of artificial intelligence, but they were not used directly. The materials were reviewed by experts in surgical nursing and related fields for clinical accuracy, consistency with current evidence, suitability for undergraduate nursing students and clarity of instruction. Necessary revisions were made according to expert feedback before the e-learning content was delivered.

Students' outcomes were assessed at three time points: before the education, immediately after the education and four weeks after the education. Knowledge of pressure injury prevention was measured using PUKAT 2.0-T. Self-efficacy in pressure injury management was measured using PUM-SES. Attitudes towards pressure injury prevention were measured using APuP. This allowed the study to examine not only immediate learning after the education but also whether learning was maintained after four weeks.

This study does not involve a direct clinical intervention with patients. The participants are nursing students. Therefore, the effect of the study on patient care is indirect. However, improving the way pressure injury prevention is taught may support future healthcare professionals' clinical decision-making and patient safety practices.

The study aims to show whether artificial intelligence-supported modular e-learning is a useful method for pressure injury prevention education, how it compares with face-to-face instruction and whether students retain what they have learned over a short follow-up period. The findings may contribute to the development of nursing education programmes, the standardisation of pressure injury prevention education and stronger patient safety-focused education strategies in tissue viability.

Tipo de estudio

Intervencionista

Inscripción (Actual)

162

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Kilis
      • Kilis, Kilis, Turquía (Türkiye), 79000
        • Kilis 7 Aralık University, Yusuf Şerefoğlu Faculty of Health Sciences, Department of Nursing

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto

Acepta Voluntarios Saludables

Descripción

Inclusion Criteria:

  • Being an undergraduate nursing student.
  • Being aged 18 years or older.
  • Voluntarily agreeing to participate in the study.
  • Providing written informed consent.
  • Being able to participate in the allocated educational intervention and scheduled outcome assessments.

Exclusion Criteria:

  • Refusing to participate in the study.
  • Having previously received additional structured education on pressure ulcer or pressure injury prevention outside the standard curriculum.
  • Being unable to complete the educational intervention due to absence or withdrawal before intervention delivery.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador activo: Face-to-Face Instruction
Participants assigned to this arm received conventional face-to-face classroom instruction on pressure injury prevention. The session covered the causes of pressure injuries, classification and observation, risk assessment, nutrition, preventive interventions, care for special patient groups, and medical device-related pressure injuries. The education was delivered using standardised presentation materials.
Participants received conventional face-to-face classroom instruction on pressure injury prevention. The session was delivered using standardised presentation materials and covered the causes of pressure injuries, classification and observation, risk assessment, nutrition, preventive interventions, care for special patient groups, and medical device-related pressure injuries.
Otros nombres:
  • Face-to-face instruction Conventional classroom instruction
Experimental: AI-Supported Modular E-Learning Programme
Participants assigned to this arm completed an artificial intelligence-supported modular e-learning programme on pressure injury prevention. The programme included short video presentations, clinical examples, question-and-answer activities, short quizzes and feedback sections. The content covered the same core pressure injury prevention topics as the face-to-face instruction and was reviewed by experts before implementation.
Participants completed an artificial intelligence-supported modular e-learning programme on pressure injury prevention. The programme included short video presentations, clinical examples, question-and-answer activities, short quizzes and feedback sections. The content covered the same core pressure injury prevention topics as the face-to-face instruction and was reviewed by experts before implementation.
Otros nombres:
  • AI-supported e-learning programme Modular e-learning programme

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Pressure Injury Prevention Knowledge Score
Periodo de tiempo: Baseline, immediately after the intervention, and 4 weeks after the intervention.

Outcome Measure Description:

Pressure injury prevention knowledge will be assessed using the Turkish version of the Pressure Injury Knowledge Assessment Tool 2.0 (PIKAT 2.0-Tr). The tool evaluates evidence-based knowledge of pressure injury prevention, including aetiology, classification and observation, risk assessment, nutrition, prevention, and care for special patient groups. The total score ranges from 0 to 24, with higher scores indicating higher levels of pressure injury prevention knowledge.

Baseline, immediately after the intervention, and 4 weeks after the intervention.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Pressure Injury Prevention Self-Efficacy Score
Periodo de tiempo: Baseline, immediately after the intervention, and 4 weeks after the intervention.

Outcome Measure Description:

Pressure injury prevention self-efficacy will be assessed using the Pressure Ulcer Management Self-Efficacy Scale (PUM-SES). This scale measures students' perceived confidence in performing pressure injury prevention and management-related activities. The total score is standardised from 0 to 100, with higher scores indicating higher perceived self-efficacy.

Baseline, immediately after the intervention, and 4 weeks after the intervention.
Change in Attitudes Towards Pressure Injury Prevention Score
Periodo de tiempo: Baseline, immediately after the intervention, and 4 weeks after the intervention.

Outcome Measure Description:

Attitudes towards pressure injury prevention will be assessed using the Attitude towards Pressure Ulcer Prevention instrument (APuP). The scale evaluates students' attitudes towards the importance, responsibility, and effectiveness of pressure injury prevention. The total score ranges from 13 to 52, with higher scores indicating more positive attitudes towards pressure injury prevention.

Baseline, immediately after the intervention, and 4 weeks after the intervention.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Director de estudio: İSLAM ELAGÖZ, PhD, Kilis 7 Aralik University

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

30 de mayo de 2025

Finalización primaria (Actual)

15 de junio de 2025

Finalización del estudio (Actual)

20 de junio de 2025

Fechas de registro del estudio

Enviado por primera vez

9 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

16 de junio de 2026

Publicado por primera vez (Actual)

18 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

16 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • kilis22222

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

No individual participant data will be shared. The study was conducted with undergraduate nursing students at a single institution, and the dataset may include educational and demographic information that could increase the risk of indirect identification. De-identified aggregate results will be reported in publications and scientific presentations.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre Face-to-Face Pressure Injury Prevention Education

  • University of Birmingham
    Heart of England NHS Trust; Calderdale and Huddersfield NHS Foundation Trust; Resuscitation...
    Terminado
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