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Video-Based Versus Bedside eFAST Training in Final-Year Medical Students

2026년 8월 25일 업데이트: Gorkem Alper Solakoglu

Comparative Effectiveness of Video-Based and Bedside Teaching for eFAST Training in Final-Year Medical Students: A Randomised Controlled Educational Trial

This study compared two methods of teaching the Extended Focused Assessment with Sonography for Trauma (eFAST) examination to final-year medical students. Participants were randomly assigned in a 1:1 ratio to either a 60-minute standardized video-based training session or a 60-minute instructor-led bedside training session. Both groups received the same educational content, for the same duration, from the same instructor.

Within one hour after completing the training, each participant performed an individual eFAST examination on a healthy volunteer. Performance was assessed by an evaluator who was unaware of the participant's training group, using an eFAST Image Acquisition Checklist. The study compared overall immediate eFAST performance between the two teaching methods and also examined performance in individual eFAST examination windows.

연구 개요

상세 설명

This was a single-center, parallel-group, individually randomized educational trial involving final-year medical students undertaking an emergency medicine clerkship. Participants with previous formal ultrasound training or prior practical ultrasound experience were excluded. One hundred consenting participants were randomized, with 50 assigned to standardized video-based eFAST training and 50 assigned to instructor-led bedside eFAST training.

Both interventions lasted 60 minutes and covered the same theoretical and practical eFAST content. Participants underwent an individual practical assessment on a healthy volunteer within one hour after training. Outcome assessors were blinded to training allocation. Performance was assessed using an eFAST Image Acquisition Checklist, which generated an overall score ranging from 0 to 100 and window-specific classifications of error-free performance.

No primary outcome was designated in advance of the analysis. For the present report and retrospective trial registration, the overall eFAST performance score is designated as the primary outcome, while the window-level comparisons are considered exploratory secondary outcomes.

연구 유형

중재적

등록 (실제)

100

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Istanbul
      • Kadıköy, Istanbul, 터키 (Türkiye)
        • Istanbul Medeniyet University

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

예

설명

Inclusion Criteria:

Current enrollment as a final-year (sixth-year) medical student at İstanbul Medeniyet University Faculty of Medicine.

Participation in the emergency medicine clerkship during the study period. Provision of written informed consent before randomization.

Exclusion Criteria:

Previous formal ultrasound training. Prior practical ultrasound experience. A physical condition that could interfere with performing an ultrasound examination.

Declining or not providing written informed consent.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 다른
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Video-Based eFAST Training
Participants received a 60-minute standardized video-based eFAST training session. The video was recorded on a healthy volunteer and covered the theoretical principles and practical performance of eFAST, including clinical indications, ultrasound physics, examination windows, transducer selection, probe positioning and orientation, image optimization, normal anatomical landmarks, and representative pathological images.
Participants watched a standardized 60-minute instructional video covering the theoretical principles and practical performance of eFAST. The video was recorded on a healthy volunteer and included demonstrations of the examination with visual annotation. Content included the principles and clinical indications of eFAST, ultrasound physics, examination windows, transducer selection, probe positioning and orientation, image optimization, normal anatomical landmarks, and representative pathological images.
활성 비교기: Instructor-Led Bedside eFAST Training
Participants received a 60-minute instructor-led bedside eFAST training session on a healthy volunteer. The session covered the same theoretical and practical content as the video-based intervention and included live demonstration of each eFAST examination window followed by supervised practice, during which each participant performed the examination once under direct guidance.
Participants received a 60-minute instructor-led bedside training session delivered by the same emergency physician on a healthy volunteer. The session covered the same theoretical and practical eFAST content as the video-based intervention and included live demonstration of each examination window followed by supervised practice, during which each participant performed the examination once under direct guidance.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Overall eFAST Performance Score
기간: Within 1 hour after completion of the assigned training session
Overall practical eFAST performance was assessed using the eFAST Image Acquisition and Interpretation Assessment Checklist. The checklist comprised 21 image-acquisition items across six eFAST windows and one image-differentiation component. Image-acquisition items contributed a maximum of 84 points and image differentiation contributed a maximum of 16 points, yielding a total score from 0 to 100, with higher scores indicating better performance. For this retrospective registration, the overall performance score is designated as the primary outcome; no primary outcome was prospectively designated before the analysis.
Within 1 hour after completion of the assigned training session

2차 결과 측정

결과 측정
측정값 설명
기간
Error-Free Anterior Lung Window Performance
기간: Within 1 hour after completion of the assigned training session
Proportion of participants who completed all required steps for the anterior lung eFAST window correctly. Any incorrectly performed required step resulted in classification as not error-free.
Within 1 hour after completion of the assigned training session
Error-Free Subxiphoid Window Performance
기간: Within 1 hour after completion of the assigned training session
Proportion of participants who completed all required steps for the subxiphoid eFAST window correctly. Any incorrectly performed required step resulted in classification as not error-free.
Within 1 hour after completion of the assigned training session
Error-Free Right Upper Quadrant Window Performance
기간: Within 1 hour after completion of the assigned training session
Proportion of participants who completed all required steps for the right upper quadrant eFAST window.correctly. Any incorrectly performed required step resulted in classification as not error-free.
Within 1 hour after completion of the assigned training session
Error-Free Left Upper Quadrant Window Performance
기간: Within 1 hour after completion of the assigned training session
Proportion of participants who completed all required steps for the left upper quadrant eFAST windowcorrectly. Any incorrectly performed required step resulted in classification as not error-free.
Within 1 hour after completion of the assigned training session
Error-Free Pelvic Window Performance
기간: ithin 1 hour after completion of the assigned training session
Proportion of participants who completed all required steps for the pelvic eFAST window correctly. Any incorrectly performed required step resulted in classification as not error-free.
ithin 1 hour after completion of the assigned training session

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 8월 1일

기본 완료 (실제)

2025년 11월 30일

연구 완료 (실제)

2025년 11월 30일

연구 등록 날짜

최초 제출

2026년 8월 25일

QC 기준을 충족하는 최초 제출

2026년 8월 25일

처음 게시됨 (실제)

2026년 8월 27일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 27일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 8월 25일

마지막으로 확인됨

2026년 8월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

De-identified individual participant data underlying the reported results may be made available by the corresponding author upon reasonable request. Public deposition of individual-level data is not planned because the participant consent did not cover public data deposition. Requests will be considered in accordance with applicable ethical and institutional requirements.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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