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Self-Directed Learning for Pulmonary Ultrasound Education

29 de junio de 2026 actualizado por: Samuel Agostino, University of Turin, Italy

"Scaling Up Ultrasound Education Without Scaling Up Tutors: A Randomized Controlled Equivalence Trial of Self-Directed Learning for Pulmonary Pathology Recognition"

This study compared two ways of teaching medical students how to recognize lung conditions using ultrasound images.

All participants were third-year medical students taking part in a structured ultrasound training session at the University of Turin. Students were randomly assigned to one of two groups. One group learned lung ultrasound pathology recognition with direct guidance from a tutor. The other group used a self-directed digital learning tool called MEDQUIZ, which allowed students to review clinical cases and ultrasound videos independently.

The main goal of the study was to determine whether self-directed learning was equivalent to tutor-guided instruction for recognizing pulmonary ultrasound findings. Students completed ultrasound image-based assessments before and after the training. The assessments evaluated their ability to recognize anatomical structures, distinguish normal from abnormal findings, and identify specific lung conditions such as pneumonia, pleural effusion, interstitial syndrome, and pneumothorax.

The study also evaluated student satisfaction with the learning experience.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Descripción detallada

This was a single-center, randomized, controlled equivalence trial conducted at the SimTO Advanced Medical Simulation Center, University of Turin, Italy. The study included third-year medical students enrolled in the curricular "Approach to Ultrasound" internship.

Before the in-person training session, all students completed online instructional materials on thoracic and abdominal ultrasound. During the internship, students participated in a structured two-hour ultrasound training session composed of four 30-minute stations. The stations included hands-on scanning of healthy volunteers and case-based pathology recognition activities.

At the thoracic pathology station, students were randomly assigned to either tutor-guided learning or self-directed learning. In the tutor-guided group, students worked through pulmonary ultrasound cases with direct supervision, clinical reasoning guidance, and feedback from a tutor. In the self-directed learning group, students used MEDQUIZ, a purpose-built digital learning tool that presented clinical cases, patient information, and lung ultrasound video clips in an interactive format.

The primary outcomes were based on pre-training and post-training assessments using ultrasound video cases. Students were assessed on three levels of competency: recognition of the anatomical structure shown in the ultrasound clip, classification of the finding as physiological or pathological, and identification of the specific pulmonary condition when a pathological finding was present. An overall case resolution score was also calculated.

Secondary outcomes included student satisfaction with the simulation-based learning experience, assessed at the end of the internship.

Tipo de estudio

Intervencionista

Inscripción (Actual)

385

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

    • Italy
      • Turin, Italy, Italia, 10126
        • Advanced Medical Simulation Center- SimTO, School of Medicine, Turin, Italy

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

Descripción

Inclusion Criteria:

  • Third-year medical students enrolled in the "Approach to Ultrasound" curricular internship at the University of Turin
  • Limited or no prior ultrasound experience
  • No previous formal specialized ultrasound training
  • Provision of informed consent for data collection

Exclusion Criteria:

  • Inability to attend the complete ultrasound training session and both assessment sessions
  • Physical or medical conditions limiting participation in hands-on ultrasound practice
  • Refusal to provide informed consent for data collection

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
Comparador activo: Tutor-Guided Learning
Participants assigned to this arm completed the thoracic pathology recognition station with direct tutor guidance. During the session, students reviewed pulmonary ultrasound cases through structured case-based learning, received real-time clinical reasoning guidance, and were provided with immediate corrective feedback by a trained tutor. All other components of the ultrasound internship were identical to those completed by the self-directed learning group.
Participants completed the thoracic pathology recognition station with direct tutor guidance. During the 30-minute station, students reviewed pulmonary ultrasound cases through structured case-based learning, received real-time clinical reasoning guidance, and were provided with immediate corrective feedback by a trained tutor.
Experimental: Self-Directed Learning
Participants assigned to this arm completed the thoracic pathology recognition station using MEDQUIZ, a purpose-built self-directed digital learning tool. Students independently reviewed clinical cases, patient information, and pulmonary ultrasound video clips without structured tutor guidance. The tool included learning materials that remained available during the session. All other components of the ultrasound internship were identical to those completed by the tutor-guided learning group.
Participants used MEDQUIZ, a purpose-built digital learning tool, to complete the thoracic pathology recognition station independently. The tool presented clinical cases, patient information, learning materials, and pulmonary ultrasound video clips. Students reviewed the cases and answered independently without structured tutor guidance during the 30-minute station.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Anatomical Structure Recognition Accuracy
Periodo de tiempo: Immediately before and immediately after the 3-hour ultrasound training session
Percentage of pulmonary ultrasound cases in which participants correctly identified the anatomical structure shown in the ultrasound video clip.
Immediately before and immediately after the 3-hour ultrasound training session
Physiological Versus Pathological Discrimination Accuracy
Periodo de tiempo: Immediately before and immediately after the 3-hour ultrasound training session
Percentage of pulmonary ultrasound cases in which participants correctly classified the ultrasound finding as physiological or pathological.
Immediately before and immediately after the 3-hour ultrasound training session
Pulmonary Pathology Identification Accuracy
Periodo de tiempo: Immediately before and immediately after the 3-hour ultrasound training session
Percentage of pathological pulmonary ultrasound cases in which participants correctly identified the specific pulmonary condition shown in the ultrasound video clip, including pneumonia or consolidation, interstitial syndrome, pleural effusion, or pneumothorax.
Immediately before and immediately after the 3-hour ultrasound training session
Overall Pulmonary Ultrasound Case Resolution Score
Periodo de tiempo: Immediately before and immediately after the 3-hour ultrasound training session
Percentage of pulmonary ultrasound cases correctly resolved with the maximum score. A case was considered correctly resolved when the participant correctly identified the anatomical structure, correctly classified the finding as physiological or pathological, and, where applicable, correctly identified the specific pulmonary pathology.
Immediately before and immediately after the 3-hour ultrasound training session

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Student Satisfaction With the Simulation Experience
Periodo de tiempo: Immediately after the 3-hour ultrasound training session
Student satisfaction with the ultrasound training experience will be assessed after the session using the Italian version of the Satisfaction with Simulation Experience scale. This scale includes 18 items rated on a 5-point Likert scale, from 1 to 5. The total score ranges from 18 to 90, with higher scores indicating greater satisfaction with the simulation-based learning experience. Three subscale scores will also be calculated: Debriefing and Reflection, ranging from 9 to 45; Clinical Reasoning, ranging from 5 to 25; and Clinical Learning, ranging from 4 to 20. For all subscales, higher scores indicate a better outcome, corresponding to greater satisfaction in the specific domain.
Immediately after the 3-hour ultrasound training session

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Director de estudio: Alberto Milan, PhD, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy

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)

3 de marzo de 2026

Finalización primaria (Actual)

30 de abril de 2026

Finalización del estudio (Actual)

30 de abril de 2026

Fechas de registro del estudio

Enviado por primera vez

23 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

29 de junio de 2026

Publicado por primera vez (Actual)

1 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de julio de 2026

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

29 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 219865

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 made publicly available. Access to de-identified data may be considered only in the context of a formal scientific collaboration and after approval by the relevant institutional and ethics committee authorities, in accordance with applicable 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. .