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The Effectiveness of Situation Awareness Approach on Nursing Competencies in Obstetric Practicum: A Multimodal Teaching

24 de septiembre de 2026 actualizado por: Yu-Yun Hsu, National Cheng Kung University

The declining birth rate and the complex and unpredictable nature of obstetric clinical situations have limited nursing students' opportunities to gain authentic clinical experience and increased the challenges and stress associated with obstetric practicum. Therefore, undergraduate nursing students preparing for obstetric clinical practice require adequate pre-clinical preparation to develop essential competencies in situation awareness, communication, clinical reasoning, and decision-making. However, traditional teaching approaches may not adequately replicate authentic obstetric situations or provide sufficient opportunities for students to integrate knowledge and respond appropriately to dynamic clinical conditions.

This study aims to develop a Situation Awareness-Based Multimodal Instructional (SAMI) program for undergraduate nursing students. The program integrates situation awareness theory, multimodal learning, virtual simulation, and game-based learning, incorporating visual, auditory, tactile, movement, and spatial experiences to create immersive and context-based obstetric learning environments. The SAMI program is designed to prepare nursing students for clinical practice by enhancing their ability to recognize relevant clinical cues, understand patient conditions, anticipate potential changes, and make appropriate clinical judgments and decisions.

First, the feasibility, usability, and learner experiences of the SAMI program will be examined. Approximately 28 undergraduate nursing students who initail their obstetric clinical practicum will be recruited. They are allocated into 4 groups and randomly be assigned experimental groups or control groups. The experimental group will received SAMI program teaching; while control group will receive usual teaching. Subsequently, to evaluate the effectiveness of the program, undergraduate nursing students across different educational institutions will be cruited during their obstetric practicum. The research outcomes will include situation awareness, obstetric communication, clinical reasoning, and confidence in clinical decision-making. Finally, this study will examine a model including educational background, obstetric practicum stress, situation awareness, and core competencies in maternal nursing care. We plan to recruite 300 nursing students to test the model.

Ultimately, this study aims to establish an evidence-based, context-based, and multimodal pre-clinical preparation model that bridges the gap between classroom learning and obstetric clinical practice. The findings will provide empirical evidence on the effectiveness of the SAMI program in enhancing nursing students' clinical readiness and core competencies for obstetric practicum.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

455

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

  • Nombre: Yu-Yun Hsu, Doctoral degree
  • Número de teléfono: 5036 886-62353535
  • Correo electrónico: yuht12@mail.ncku.edu.tw

Copia de seguridad de contactos de estudio

  • Nombre: Tsai Wan-Yu, Graduate Student
  • Número de teléfono: 5036 886-62353535
  • Correo electrónico: wendy55132@gmail.com

Ubicaciones de estudio

      • Tainan, Taiwán, 701
        • Department of Nursing, National Cheng Kung University

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

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Undergraduate nursing students aged 18 years or older.
  • Students who are about to begin their obstetric nursing practicum.
  • Full-time nursing students.

Exclusion Criteria:

  • Students who have already completed an obstetric nursing practicum.
  • Students who are repeating an obstetric nursing practicum.
  • Students with previous obstetric clinical work experience or who are currently working in an obstetric clinical setting.

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: Situation Awareness-Based Multimodal Instructional

An immersive, multisensory teaching approach that integrates clinical scenarios to enhance students' situation awareness and decision-making skills.

An immersive, multisensory teaching approach that integrates clinical scenarios to enhance students' situation awareness and decision-making skills.

Comparador de placebos: Usual-video instruction.

The control group receives video-based instruction on obstetric nursing care.

The control group receives video-based instruction on obstetric nursing care.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Outcome Measures
Periodo de tiempo: Three time points: T0, the first week of the practicum as the baseline assessment; T1, two weeks after the teaching intervention as the first post-test; and T2, within one week after completion of the practicum as the second post-test.

Situation Awareness Global Assessment Technique (SAGAT) will be used to assess situation awareness based on Endsley's theory. Each item is scored according to response accuracy, with 1 point for a correct response and 0 points for an incorrect. Maternal Nursing Practicum Stress Scale (MNPSS) will be used to assess practicum stress, containing 30 items. Each item is rated on a 5-point Likert scale from 1 (none) to 5 (very high). Critical Thinking Disposition Scale assesses the frequency of critical thinking, each item scored on a 6-point Likert scale from 1 (never) to 6 (always).Communication Self-Confidence in Maternity Scale assesses confidence in nurse-patient communication. Each item is scored on a 5-point Likert scale from 1 (very low confidence) to 5 (very high confidence). Clinical Decision-Making Self-Confidence Scale measures confidence in decision-making. Items are rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree).

Three time points: T0, the first week of the practicum as the baseline assessment; T1, two weeks after the teaching intervention as the first post-test; and T2, within one week after completion of the practicum as the second post-test.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este 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)

25 de septiembre de 2026

Finalización primaria (Estimado)

31 de diciembre de 2028

Finalización del estudio (Estimado)

31 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

18 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de septiembre de 2026

Publicado por primera vez (Actual)

28 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

28 de septiembre de 2026

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

24 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • A-ER-114-453

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data will not be shared with other researchers to protect participants' privacy, confidentiality, and rights.

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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