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Case-Based Learning for Bedside Lung Ultrasound Teaching in ICU

14 de maio de 2026 atualizado por: Qiancheng Xu, First Affiliated Hospital of Wannan Medical College

CBL Mode in Clinical Teaching of Bedside Lung Ultrasound in Intensive Care Unit: A Randomized Controlled Study

This single-center randomized controlled study aims to evaluate the effectiveness of Case-Based Learning (CBL) compared with traditional teaching in clinical training of bedside lung ultrasound (BLUE) for emergency medicine residents and medical students. The hypothesis is that CBL improves theoretical understanding, practical ultrasound skills, and clinical reasoning in emergency settings.

Visão geral do estudo

Descrição detalhada

This single-center randomized controlled educational trial will be conducted in the Intensive Care Unit (ICU) of the First Affiliated Hospital of Wannan Medical College, China. The study aims to compare the effectiveness of Case-Based Learning (CBL) and traditional lecture-based teaching in bedside lung ultrasound (BLUE) education for residents and medical students participating in critical care rotations.

Participants will be randomized in a 1:1 ratio by computer-generated sequence into either the CBL group or the traditional teaching group. Both groups will receive a total of 8 hours of instruction delivered in two 4-hour sessions during their ICU rotation period.

In the CBL group, teaching will be guided by authentic clinical cases that include varied respiratory pathologies (e.g., pneumonia, pneumothorax, pulmonary edema). Each case will involve small-group discussion of diagnostic reasoning, interpretation of ultrasound findings, and supervised scanning practice at the bedside. Instructors will facilitate feedback and reflective learning, integrating theoretical concepts with clinical application.

In the traditional teaching group, participants will attend classroom lectures on ultrasound principles and watch instructor-led demonstrations of standardized BLUE examination techniques. Short hands-on practice sessions will follow under supervision but without case-based discussion or peer-feedback components.

All teaching sessions will be delivered by faculty certified in critical ultrasonography, using standardized instruction materials and the same ultrasound equipment and scanning protocols across groups. Data collection will occur within one week after completion of the teaching intervention. Primary outcomes include Objective Structured Clinical Examination (OSCE) score reflecting image acquisition, interpretation, and clinical reasoning. Secondary outcomes comprise written knowledge test scores and learner-reported measures of learning motivation and satisfaction.

All analyses will follow the intention-to-treat principle. Group differences will be tested using appropriate statistical methods (e.g., independent t-test or Mann-Whitney U test for continuous variables and chi-square test for categorical variables). The results will provide empirical evidence to guide optimization of bedside lung ultrasound education and the implementation of interactive, case-based teaching strategies in the context of intensive and emergency care training programs.

Tipo de estudo

Intervencional

Inscrição (Estimado)

106

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Anhui
      • Wuhu, Anhui, China, 241001
        • The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College)
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho
  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Standardized residency trainees currently rotating in the Intensive Care Unit (ICU), specializing in Internal Medicine, Surgery, Emergency Medicine, Anesthesiology, or General Practice.
  • Have completed institutional basic ultrasound theory training or possess preliminary ultrasound knowledge.
  • Voluntarily participate and provide written informed consent.
  • Able to complete the entire teaching and evaluation schedule (including written test and OSCE).

Exclusion Criteria:

  • Prior formal training or certification in lung/critical care ultrasound.
  • Unable to complete the study period due to rotation scheduling or absence.
  • Decline or withdraw informed consent.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Pesquisa de serviços de saúde
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Case-Based Learning (CBL) Group
Participants study authentic emergency cases, analyze lung ultrasound images, perform bedside scanning under instructor facilitation, and discuss diagnostic reasoning in small groups.
Participants study authentic emergency cases, analyze lung ultrasound images, perform bedside scanning under instructor facilitation, and discuss diagnostic reasoning in small groups.
Comparador Ativo: Traditional Teaching Group
Participants receive conventional didactic lectures and instructor demonstration of BLUE examination followed by limited practice.
Participants receive conventional didactic lectures and instructor demonstration of BLUE examination followed by limited practice.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Objective Structured Clinical Examination (OSCE) Total Score
Prazo: Within one week after completion of the teaching sessions

he Objective Structured Clinical Examination (OSCE) total score (0-100 points) evaluates overall bedside lung ultrasound proficiency. It includes five weighted stations: (1) image acquisition and scanning technique (20 points), (2) image interpretation (20 points), (3) clinical decision-making (20 points), (4) structured case reporting and teamwork (20 points), and (5) emergency communication with patients or families (20 points). Each station is rated by three blinded assessors using standardized checklists and global rating scales. Higher scores indicate better ultrasound performance and clinical reasoning ability.

Scale Range: 0 (poor performance) to 100 (excellent performance); higher = better

Within one week after completion of the teaching sessions

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Written Theoretical Knowledge Test Score
Prazo: Within one week after the intervention

Description: Written examination assessing understanding of lung ultrasound principles, BLUE protocol workflow, and case analysis. The test includes multiple-choice, multiple-response, short-answer, and case-analysis items. Total score ranges from 0 to 100 points. Higher scores indicate greater theoretical knowledge mastery.

Scale Range: 0 (lowest) to 100 (highest); higher = better

Within one week after the intervention
Clinical Decision Substation Score
Prazo: Within one week after intervention

Description: Subscore from the Objective Structured Clinical Examination (OSCE) Station 3, evaluating diagnostic reasoning and initial management decisions based on bedside lung ultrasound findings. Scored on a 0-20 point checklist by blinded assessors. Higher values reflect stronger clinical decision-making ability.

Scale Range: 0 (lowest) to 20 (highest); higher = better

Within one week after intervention
Self-Assessment Questionnaire Scores
Prazo: Within one week after the intervention

Description: Study-specific questionnaire evaluating self-perceived improvement in learning motivation, clinical reasoning, teamwork, and communication. Each dimension consists of 5 dichotomous items (Yes = 1; No = 0). Scores are summarized as the proportion (%) of participants responding "Yes" in each domain. The possible range is 0%-100%; higher proportions indicate more participants reporting improvement.

Scale Range: 0%-100%; higher = better perceived improvement

Within one week after the intervention
Overall Learning Satisfaction Rating
Prazo: Within one week after the intervention

Description: Overall satisfaction measured by a single 5-point Likert-type item (1 = Very dissatisfied, 2 = Dissatisfied, 3 = Neutral, 4 = Satisfied, 5 = Very satisfied). Reported as the proportion (%) of participants rating ≥4. Higher proportions reflect greater satisfaction with the assigned teaching method.

Scale Range: 1-5 for individual ratings; 0%-100% for proportion ≥4; higher = better satisfaction

Within one week after the intervention

Colaboradores e Investigadores

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de julho de 2026

Conclusão Primária (Estimado)

30 de junho de 2027

Conclusão do estudo (Estimado)

30 de junho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

10 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de maio de 2026

Primeira postagem (Real)

18 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

18 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

14 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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