Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID07541768

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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

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

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Training

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

Outpatient Treatment

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

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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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