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

25. August 2026 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

100

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Istanbul
      • Kadıköy, Istanbul, Türkei (türkiye)
        • Istanbul Medeniyet University

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Sonstiges
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Single

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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.
Aktiver Komparator: 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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Overall eFAST Performance Score
Zeitfenster: 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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Error-Free Anterior Lung Window Performance
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

1. August 2025

Primärer Abschluss (Tatsächlich)

30. November 2025

Studienabschluss (Tatsächlich)

30. November 2025

Studienanmeldedaten

Zuerst eingereicht

25. August 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

25. August 2026

Zuerst gepostet (Tatsächlich)

27. August 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

27. August 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

25. August 2026

Zuletzt verifiziert

1. August 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

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.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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