Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

AI-Supported Gamified Training for Sharps Injury Prevention in Nurses

26 de abril de 2026 actualizado por: İsmail Kuşoğlu, Baskent University

The Effect of An Artifıcial Intelligence-Supported Gamifıed Training Program on Nurses' Knowledge and Attitudes Toward The Prevention of Sharps Injuries

This study aims to evaluate the effect of a Health Belief Model (HBM)-based, artificial intelligence (AI)-supported gamified training program on nurses' knowledge and attitudes toward the prevention of sharps injuries. Sharps injuries remain a significant occupational risk for healthcare workers, particularly nurses, despite existing standard precautions.

The study will be conducted in two phases. In the first phase, the validity and reliability of the Sharps Injury Prediction Scale will be tested in a nurse population. In the second phase, a quasi-experimental pretest-posttest control group design will be used to assess the effectiveness of the intervention.

The study will be carried out in two hospitals from the same healthcare group located in different cities to prevent interaction between groups. A total of 36 nurses will be included, with 18 participants in the intervention group and 18 in the control group.

The intervention group will receive a structured, HBM-based training program consisting of seven sessions incorporating AI-supported content, gamified scenarios, interactive materials, and feedback mechanisms to enhance engagement and promote behavior change. The control group will receive routine institutional training on sharps injury prevention.

Data will be collected at baseline, immediately after the intervention, and two months later. Outcome measures include nurses' knowledge, attitudes toward safe sharps use, and sharps injury risk perception.

It is expected that the AI-supported gamified training program will significantly improve knowledge, attitudes, and risk awareness compared to routine training. The findings may support the integration of innovative, theory-based educational interventions into institutional training programs to enhance occupational safety.

Descripción general del estudio

Descripción detallada

Sharps injuries are among the most common occupational hazards for healthcare workers, particularly nurses, due to their frequent exposure to invasive procedures and contact with blood and body fluids. These injuries are associated with the risk of transmission of serious infections such as hepatitis B, hepatitis C, and HIV. Despite the implementation of standard precautions and institutional training programs, the incidence of sharps injuries remains a significant concern, highlighting the need for more effective and behavior-focused educational interventions.

Traditional training methods are often limited in their ability to promote sustained behavioral change. In this context, theory-based and technology-supported approaches may provide more effective solutions. The Health Belief Model (HBM) is widely used to explain and predict health-related behaviors by focusing on individuals' perceptions of risk, benefits, barriers, and self-efficacy. Integrating HBM into educational interventions may enhance the effectiveness of training programs aimed at improving safe practices.

In addition, recent advances in artificial intelligence (AI) and gamification have introduced innovative opportunities in health education. AI-supported systems can provide personalized learning experiences, while gamification techniques, such as interactive scenarios, feedback, and rewards, can increase motivation, engagement, and knowledge retention. These approaches may be particularly beneficial in nursing education, where active participation and behavioral reinforcement are essential.

This study will be conducted in two phases. In the first phase, the validity and reliability of the Sharps Injury Prediction Scale will be evaluated in a nurse population. In the second phase, a quasi-experimental pretest-posttest control group design will be used to assess the effectiveness of an HBM-based, AI-supported gamified training program.

The study will be carried out in two hospitals within the same healthcare group located in different cities to minimize interaction between groups. A total of 36 nurses will be included. The intervention group will receive a structured training program consisting of seven sessions designed based on HBM constructs, incorporating AI-supported educational materials, gamified learning tools, and interactive components. The control group will receive routine institutional training.

Data will be collected at baseline, immediately after the intervention, and two months after the intervention. Outcome measures will include knowledge levels, attitudes toward safe use of sharps, and risk perception related to sharps injuries.

The findings of this study are expected to contribute to the development of innovative, theory-based educational strategies and support the integration of AI-supported and gamified training approaches into healthcare institutions to enhance occupational safety among nurses.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

36

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.

Estudio Contacto

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

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • Registered nurses working in the participating hospitals
  • Working in the institution for at least 2 months (Phase 1) or newly employed within the last 1 month (Phase 2)
  • Willing to participate in the study
  • Able to use smartphone-based technologies
  • Providing written informed consent

Exclusion Criteria:

  • Having received prior training based on the Health Belief Model for sharps injury prevention
  • Previous professional nursing experience before current employment (for newly recruited nurses in Phase 2)
  • Being on leave during the data collection period
  • Failure to attend training sessions (intervention group)
  • Incomplete data collection forms
  • Withdrawal from the study at any stage

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: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Intervention Group
Nurses in the intervention group will receive a Health Belief Model-based, AI-supported gamified training program designed to improve knowledge and attitudes toward sharps injury prevention.
A structured training program consisting of seven sessions, incorporating artificial intelligence-supported educational content, gamified scenarios, interactive videos, and digital feedback mechanisms to enhance learning and promote behavior change.
Comparador activo: Control Group
Standard training provided by the institution, including lectures and question-answer sessions on sharps injury prevention.
Standard training provided by the institution, including lectures and question-answer sessions on sharps injury prevention.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Nurses' knowledge level regarding sharps injury prevention
Periodo de tiempo: Baseline (pretest), immediately after the intervention (posttest), and 2 months after the intervention
Knowledge level will be assessed using a structured knowledge questionnaire consisting of 25 items developed based on the literature. Higher scores indicate greater knowledge regarding sharps injury prevention.
Baseline (pretest), immediately after the intervention (posttest), and 2 months after the intervention

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Attitudes toward safe use of sharps
Periodo de tiempo: Baseline, immediately after the intervention, and 2 months after the intervention
Attitudes will be measured using the "Attitude Scale for Safe Use of Sharps Medical Instruments," a validated Likert-type scale. Higher scores indicate more positive attitudes toward safe practices.
Baseline, immediately after the intervention, and 2 months after the intervention
Sharps injury risk perception and prediction score
Periodo de tiempo: Baseline, immediately after the intervention, and 2 months after the intervention
Risk perception and prediction will be assessed using the adapted Sharps Injury Prediction Scale based on the Health Belief Model. Higher scores reflect increased perceived severity, benefits, and awareness of preventive behaviors.
Baseline, immediately after the intervention, and 2 months after the intervention

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Ziyafet Uğurlu, Professor, Baskent University

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 (Estimado)

1 de junio de 2026

Finalización primaria (Estimado)

1 de septiembre de 2026

Finalización del estudio (Estimado)

1 de junio de 2027

Fechas de registro del estudio

Enviado por primera vez

26 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

26 de abril de 2026

Publicado por primera vez (Actual)

1 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de mayo de 2026

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

26 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data (IPD) will not be shared due to ethical and privacy considerations. The study involves human participants, and sharing individual-level data may pose a risk to confidentiality despite anonymization. Data will be used solely for research purposes in accordance with ethical approval and institutional regulations.

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. .

Suscribir