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临床试验/NCT07541768
NCT07541768招募中不适用

Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment: a Randomized Controlled Trial

Insel Gruppe AG, University Hospital Bern1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2026年3月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
23
试验地点
1
主要终点
Ultrasound Image Quality Score

研究概览

简要总结

This randomized controlled trial evaluates the effectiveness of two training approaches (in-person versus remote) for teaching medical residents to apply the Venous Excess Ultrasound (VExUS) score for bedside volume assessment in patients with acute heart failure. Resident performance will be compared to that of expert physicians certified in abdominal and duplex sonography.

详细描述

Accurate assessment of volume status is essential in managing acute heart failure but remains challenging in clinical practice. The VExUS score is a validated ultrasound-based tool integrating inferior vena cava diameter and Doppler assessment of hepatic, portal, and intrarenal veins.

This single-center randomized controlled trial compares two training modalities (in-person vs. remote) in medical residents with basic ultrasound skills. Participants will be randomized 1:1 to either training method and compared to a control group of expert physicians.

Primary outcomes include ultrasound image quality assessed using a standardized 100-point score. Secondary outcomes include time to acquisition, VExUS scoring accuracy, self-confidence, and acceptability of training methods.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Medical residents in general internal medicine
  • Basic ultrasound skills (POCUS component 1 or ≥200 scans)
  • Working at study site during study period

排除标准

  • SGUM certification in abdominal ultrasound
  • Advanced duplex ultrasound experience
  • Prior vascular/duplex training

研究组 & 干预措施

In-person Training

Experimental

1-hour theoretical introduction 3-hour supervised practical ultrasound session Group-based hands-on training with expert coach

干预措施: In-person VExUS Training Program (Behavioral)

Remote Training

Experimental

E-learning theoretical module 20 independently performed ultrasound exams Asynchronous expert feedback (phone/email)

干预措施: Remote VExUS Training Program (Behavioral)

Control (Expert Physicians)

Active Comparator

SGUM-certified physicians performing VExUS examinations

干预措施: No intervention (Other)

结局指标

主要结局

Ultrasound Image Quality Score

时间窗: From training until 6 months after completion of training

The primary outcome will be a quality score, adapted from a quality score used in a previous randomized controlled trial which investigated a simulator-based training program for transoesophageal echocardiography.11 The quality score will include items commonly used for assessment of ultrasound quality: angle and depth, overall clarity, visualization of the anatomical structures, focus, doppler gain, scale and baseline resulting in a maximum achievable quality score of 100 points. If multiple images of the predefined views are captured, each image will be rated, and the best rating will be kept to calculate the final score. If a view is missing, 0 point will be awarded for that view. All ultrasound images will be independently assessed by experts for abdominal sonography and use Doppler sonography in their daily clinical practice and are blinded to the role (resident vs. SGUM-certified physician) and training (in-person vs. remote) program of the participants.

次要结局

  • Time for Image Acquisition and Interpretation(From training until 6 months after completion of training)
  • Change in self-confidence in performing VExUS assessment(From baseline (before training) to immediately after completion of training)
  • Acceptability of the program (quantitative assessment)(Immediately after completion of training and during the outcome assessment period (within 2 months after training))
  • VEXUS score(From training until 6 months after completion of training)
  • Acceptability of the program (qualitative assessment)(Immediately after completion of training and during the outcome assessment period (within 2 months after training))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Claudio Schneider

Senior physician

Insel Gruppe AG, University Hospital Bern

研究点 (1)

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