Actively Recruiting
Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment: a Randomized Controlled Trial
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2026-04-21
23
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This trial investigates two different training methods— in-person and remote— to teach medical residents how to use the Venous Excess Ultrasound (VExUS) score for bedside volume assessment in patients with acute heart failure. The study compares the residents' performance to that of expert physicians certified in abdominal and duplex sonography. Accurate volume assessment is crucial in managing acute heart failure but is challenging in clinical practice, making this training important. Participants are randomly assigned to one of two training groups. The in-person group receives a 1-hour theoretical session plus a 3-hour supervised hands-on ultrasound training focusing on VExUS score acquisition and interpretation. The remote group completes an e-learning module followed by 20 independent ultrasound exams with expert feedback provided asynchronously via phone or email. Expert physicians certified in VExUS serve as a control group. Throughout and up to six months after training, researchers will assess ultrasound image quality using a standardized 100-point score. They will also measure time for image acquisition and interpretation, accuracy of VExUS scoring, participants’ confidence in performing the assessment, and how acceptable each training method is. These evaluations include both quantitative and qualitative assessments during and after the training period. The trial is led by Insel Gruppe AG and University Hospital Bern.
CONDITIONS
Brief Title
Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Medical residents in general internal medicine
- Basic ultrasound skills (POCUS component 1 or 200 scans)
- Working at study site during study period
You will not qualify if you...
- SGUM certification in abdominal ultrasound
- Advanced duplex ultrasound experience
- Prior vascular/duplex training
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants receive either in-person or remote training on the use of the VExUS ultrasound score, including theoretical introduction and practical ultrasound sessions.
1 to 2 visits depending on training modality
Duration - Up to 6 months after completion of training
Participants perform ultrasound examinations with ongoing assessments of image quality, acquisition time, scoring accuracy, and self-confidence.
Ongoing assessments during training and up to 6 months after
Trial Site Locations
Total: 1 location
1
Inselspital
Bern, Switzerland, 3011
Actively Recruiting
Research Team
C
Caroline Rimensberger, MD
C
Claudio Schneider, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
3
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