Evaluation of Hydrogel Versus Human Cadaver Models for Training in Robot-Assisted Radical Prostatectomy
Led by Orsi Academy · Updated on 2026-06-25
56
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
This research aims to evaluate training methods for robot-assisted radical prostatectomy RARP, a complex robotic surgery procedure requiring structured skill development. The study compares a new training pathway that uses a synthetic IMRA Surgical Prostatectomy Class V Hydrogel Model to the standard training pathway that uses biological human cadaver models. The goal is to determine if the hydrogel model provides training outcomes that are as effective as the traditional method, addressing ethical and scalability challenges in surgical education.
Participants enrolled in a five-day standardized robotic surgery training course will be randomly assigned to one of two groups. One group trains on the hydrogel model during the fourth day, while the other group trains on human cadaver models on the same day. Both groups then complete a final assessment using human cadaver training on the fifth day. The training includes supervision, defined learning objectives, and performance assessments based on validated metrics.
During the study, participants technical skills, errors, confidence levels, readiness to perform RARP, and cognitive workload will be measured through assessments and questionnaires. The primary outcome is the proportion of participants meeting proficiency criteria at the final cadaver assessment. The study also evaluates the feasibility and acceptability of the hydrogel model in surgical training. Participation lasts for the full training course, with evaluations conducted at key points.
CONDITIONS
Brief Title
Comparing Two Training Methods for Learning Robot-Assisted Radical Prostatectomy
Research Team
E
Eva Vanderstraeten
N
Niki Rashidian
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Enrollment in the CC-ERUS training course or attending the same robotic RARP training course at ORSI Academy during the study period
Willingness and ability to provide informed consent for participation
You will not qualify if you...
Decline or inability to provide informed consent
Incomplete participation in the on-site training course preventing assessment on Day 5
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Training
Duration - 5 days
Participants undergo a five-day robotic surgery training course. On Day 4, one group trains using the hydrogel model while the other uses human cadaver models. Both groups complete final assessment training on human cadavers on Day 5.
Daily training sessions for 5 days
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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Published Research Related To This Trial
Objective assessment of intraoperative skills for robot-assisted radical prostatectomy (RARP): results from the ERUS Scientific and Educational Working Groups Metrics Initiative.