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PROficiency Based StePwise Endovascular Curricular Training: Multicentric Registry

Not Applicable
Recruiting
Conditions
Vascular Diseases
Interventions
Other: PROSPECT
Registration Number
NCT05620186
Lead Sponsor
University Hospital, Ghent
Brief Summary

The goal of this multicentric registry is to gather data from trainees completing PROSPECT: a PROficiency Based StePwise Endovascular Curricular Training to obtain basic cognitive and technical skills. The main goals are to identify if:

* Results from a previous randomised controlled trail can be reproduced in real life.

* Evaluate skills retention after program completion.

* Assess real life implementation of the training program.

Detailed Description

A validated PROSPECT (PROficiency-based StePwise Endovascular Curricular Training) training has been integrated into the training of surgical residents to teach basic cognitive, technical and non-technical endovascular skills. The program uses virtual reality simulation and E-learning. During the four modules of the program, formative feedback is given after each training session. Only after achieving a predetermined benchmark score, trainees can progress to the next module.

Surgical trainees completing PROSPECT showed superior real live endovascular performance compared to the traditionally trained in a single centre randomised controlled trial (RCT). The curriculum was integrated locally, but also introduced in other centers: national and international. Local tutors teach the curriculum to trainees after standardized training on the modalities of PROSPECT by the researchers of the Ghent.

A registry is maintained and coordinated by the Ghent research group in which all educational data regarding this training is collected and processed anonymously.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Surgical trainee
  • Knowledge and technical skill level evaluated
  • Demographics questionnaire and general MCQ test completed
  • Endovascular simulated exercise completed after familiarization with the simulator
Exclusion Criteria
  • N/A

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Massed PROSPECTPROSPECTMassed, bootcamp-style training form of PROSPECT where trainees are exempt from clinical duties
Original PROSPECTPROSPECTOriginal, distributed PROSPECT where trainees learn at their own pace in between, before/after clinical activities
Primary Outcome Measures
NameTimeMethod
Cognitive skillscomparison before program start and after completion. This means through study completion.

Multiple Choice Question test (min: 0, max: 20, the higher the score, the better)

Technical skillscomparison before program start and after completion. This means through study completion.

Rating scale assessment and simulator metrics

Secondary Outcome Measures
NameTimeMethod
Technical skills retention3, 6 and 12 months after program completion

Rating scale assessment and simulator metrics

Cognitive skills retention3, 6 and 12 months after program completion

Multiple Choice Question test (min: 0, max: 20, the higher the score, the better)

Trial Locations

Locations (3)

KU Leuven

🇧🇪

Leuven, Belgium

CAMES

🇩🇰

Copenhagen, Denmark

University Hospital Ghent

🇧🇪

Ghent, Belgium

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