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Clinical Trials/NCT05620186
NCT05620186RecruitingNot Applicable

Registry Endovascular Training Curriculum PROSPECT for Surgical Trainees (PROficiency-based StePwise Endovascular Curricular Training Program)

University Hospital, Ghent3 sites in 2 countries120 target enrollmentStarted: October 17, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
120
Locations
3
Primary Endpoint
Cognitive skills

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

  • Not provided

Arms & Interventions

Original PROSPECT

Other

Original, distributed PROSPECT where trainees learn at their own pace in between, before/after clinical activities

Intervention: PROSPECT (Other)

Massed PROSPECT

Other

Massed, bootcamp-style training form of PROSPECT where trainees are exempt from clinical duties

Intervention: PROSPECT (Other)

Outcomes

Primary Outcomes

Cognitive skills

Time Frame: comparison 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 skills

Time Frame: comparison before program start and after completion. This means through study completion.

Rating scale assessment and simulator metrics

Secondary Outcomes

  • Technical skills retention(3, 6 and 12 months after program completion)
  • Cognitive skills retention(3, 6 and 12 months after program completion)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (3)

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