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Web-Based Gamified Simulation for Teaching Ventrogluteal Injection to First-Year Nursing Students

6 de octubre de 2026 actualizado por: Gözde ÖZARAS ÖZ, Çankırı Karatekin University

The Effect of Web-Based Gamified Simulation for Ventrogluteal Injection Training on Knowledge, Skills, Satisfaction, and Self-Confidence Among First-Year Nursing Students: A Randomized Controlled Trial

The goal of this study is to find out whether a web-based simulation with game features helps first-year nursing students learn how to give an injection into the muscle on the side of the hip, known as the ventrogluteal site. The study will compare this approach with traditional teaching at Cankiri Karatekin University in Türkiye.

The main questions are whether the web-based simulation improves students' knowledge and practical skills, increases their satisfaction and confidence in learning, and helps them remember what they have learned after eight weeks.

All participants will receive the same initial classroom teaching and laboratory demonstration. They will then be assigned by chance to one of two groups. One group will receive traditional teaching. The other group will use the web-based simulation, which includes a patient scenario and interactive tasks, such as selecting equipment and moving items to a tray.

The simulation has two modes. In the learning mode, students receive hints and explanations without being scored. In the self-test mode, they complete tasks without hints and receive a score report for feedback. Students must answer correctly before moving to the next step.

Participants will complete a knowledge test, a practical skills assessment using an injection training model, and a questionnaire about satisfaction and confidence before the group-specific training and again one week afterward. They will repeat the knowledge test eight weeks after training to assess how much they remember. Practical skills will be assessed by two observers who do not know which teaching group each student belongs to.

Descripción general del estudio

Descripción detallada

This study will examine a structured approach to teaching ventrogluteal injection by combining a clinical scenario with interactive tasks, feedback, and rule-based progression in a web-based learning environment.

Before group allocation, all participants will receive four hours of theoretical instruction and four hours of standard laboratory demonstration using injection training models. Laboratory sessions will be conducted in groups of approximately 20-22 students. Baseline assessments will take place two days after this common training to establish students' starting levels before the group-specific educational activities.

Participants will be stratified by baseline knowledge test scores into two categories: scores of 10 or below and scores above 10 on the 20-point test. An independent researcher who is not involved in intervention delivery will generate the allocation sequence using blocks of four, with equal allocation to the intervention and control groups within

Tipo de estudio

Intervencionista

Inscripción (Estimado)

110

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

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Being a first-year nursing student enrolled in the Fundamentals of Nursing I course at Cankiri Karatekin University during the fall semester of the 2026-2027 academic year.
  • Taking the course for the first time.
  • Voluntarily agreeing to participate and providing written informed consent.
  • Agreeing to attend all planned theoretical, laboratory, and study sessions.

Exclusion Criteria:

  • Having difficulty understanding Turkish to an extent that prevents participation in the educational activities or completion of the assessment tools.
  • Being a graduate of a health vocational high school.
  • Having previously received formal training in intramuscular injection techniques.

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: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Web-Based Gamified Simulation

After receiving the common theoretical and laboratory training, students in this arm will use a web-based gamified simulation for ventrogluteal injection training. Students will receive standardized instructions on accessing and using the application. They will first complete the learning mode, which provides step-by-step hints and rationales without scoring, followed by the self-test mode without hints. Interactive tasks include selecting equipment, moving materials onto a tray, and making decisions about procedural steps. A correct response is required before proceeding to the next step. A final performance report will provide individual learning feedback.

A web-based gamified simulation designed to teach ventrogluteal injection through 33 procedural steps. Following standardized instructions on application use, students will complete the learning mode with hints and rationales and then the self-test mode without hints. Tasks include selecting equipment, moving materials onto a tray, and making procedural decisions. Students must provide a correct response before advancing. The self-test mode generates a performance report for individual learning feedback. Application scores will not be used as research outcome measures.

Comparador activo: Traditional Ventrogluteal Injection Training

After receiving the common theoretical and laboratory training, students in this arm will continue ventrogluteal injection training using traditional teaching methods. They will not use the web-based gamified simulation during the study.

Traditional instruction in ventrogluteal injection, including theoretical teaching and instructor-led laboratory demonstration using injection training models. Students assigned to the control arm will continue training using traditional teaching methods following the common initial theoretical and laboratory training.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Ventrogluteal Injection Knowledge Score
Periodo de tiempo: Baseline (before randomization) and 1 week after the intervention.

Knowledge will be assessed using the researcher-developed Ventrogluteal Injection Knowledge Test, which consists of 20 multiple-choice questions. Each correct answer receives 1 point, and each incorrect answer receives 0 points. Total scores range from 0 to 20, with higher scores indicating greater knowledge of ventrogluteal injection. Scores will be compared between the intervention and control groups, accounting for baseline scores.

Baseline (before randomization) and 1 week after the intervention.
Ventrogluteal Injection Skill Performance Score
Periodo de tiempo: Baseline (before randomization) and 1 week after the intervention.

Skill performance will be assessed through an Objective Structured Clinical Examination (OSCE) using a 24-item Ventrogluteal Injection Skill Checklist. Each item is scored as 0 (incorrectly performed or not performed), 1 (partially correctly performed), or 2 (correctly performed). Total scores range from 0 to 48, with higher scores indicating better skill performance. Two independent observers blinded to group allocation will assess performance simultaneously and score independently. Scores will be compared between groups, accounting for baseline scores.

Baseline (before randomization) and 1 week after the intervention.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Student Satisfaction With Learning Score
Periodo de tiempo: Baseline (after common initial training and before randomization) and 1 week after the intervention.

Satisfaction with learning will be assessed using the five-item Student Satisfaction subscale of the Turkish version of the Student Satisfaction and Self-Confidence in Learning Scale. Each item is rated from 1 (strongly disagree) to 5 (strongly agree). Total subscale scores range from 5 to 25, with higher scores indicating greater satisfaction with the learning experience. Baseline assessment will refer to the common initial training, while post-intervention assessment will refer to the training received in the assigned group.

Baseline (after common initial training and before randomization) and 1 week after the intervention.
Retention of Ventrogluteal Injection Knowledge
Periodo de tiempo: 8 weeks after the intervention.

Knowledge retention will be assessed by readministering the 20-item Ventrogluteal Injection Knowledge Test eight weeks after the intervention. Each correct answer receives 1 point, and each incorrect answer receives 0 points. Total scores range from 0 to 20, with higher scores indicating greater retained knowledge. Eight-week scores will be compared between groups and examined alongside baseline and one-week post-intervention scores.

8 weeks after the intervention.

Colaboradores e Investigadores

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

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 (Estimado)

13 de noviembre de 2026

Finalización primaria (Estimado)

20 de noviembre de 2026

Finalización del estudio (Estimado)

20 de diciembre de 2026

Fechas de registro del estudio

Enviado por primera vez

1 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

1 de octubre de 2026

Publicado por primera vez (Actual)

6 de octubre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

8 de octubre de 2026

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

6 de octubre de 2026

Última verificación

1 de octubre 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

There is no plan to share individual participant data with other researchers. Study findings will be disseminated through publications and presentations using aggregate data.

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. .

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