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NCT Number: NCT07594470

Case-Based Learning for Bedside Lung Ultrasound Teaching in ICU

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Affiliated Hospital of Wannan Medical College (Yijishan Hospital of Wannan Medical College)

Wuhu, Anhui, 241001, China

Location contact

qiancheng xu

CONTACT

[email protected]

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Case-Based Learning (CBL)

Behavioral

Participants study authentic emergency cases, analyze lung ultrasound images, perform bedside scanning under instructor facilitation, and discuss diagnostic reasoning in small groups.

Traditional lecture-based teaching

Behavioral

Participants receive conventional didactic lectures and instructor demonstration of BLUE examination followed by limited practice.

Primary outcomes

  1. Objective Structured Clinical Examination (OSCE) Total Score

    Time frame: 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

Secondary outcomes

  1. Written Theoretical Knowledge Test Score

    Time frame: 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

  2. Clinical Decision Substation Score

    Time frame: 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

  3. Self-Assessment Questionnaire Scores

    Time frame: 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

  4. Overall Learning Satisfaction Rating

    Time frame: 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

Study contacts

Contact information is provided by the study sponsor or research team.

qiancheng xu

CONTACT

[email protected]

+86-18297529106

Sponsors and collaborators

Lead sponsor

First Affiliated Hospital of Wannan Medical College

Other

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 18, 2026
Registry last updated
May 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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