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Effect of Virtual Endoscopy Simulator Training on Real Patient Endoscopy

Effect of Virtual Endoscopy Simulator Training on Real Patient Endoscopy: A Randomized, Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00576043
Acronym
endosim
Enrollment
24
Registered
2007-12-18
Start date
2004-03-31
Completion date
2008-03-31
Last updated
2008-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

training, Patient satisfaction, endoscopy, simulator, Safety

Brief summary

Trainees (Residents in internal medicine), naive to real patient endoscopy, will be randomized to receive either 3 weeks/2 hours per day of structured training for a total of 20 hours on the virtual endoscopy simulator GI-Mentor or no training before starting on-patient endoscopy in the University of Vienna Medical School Endoscopy Unit. Patients satisfaction and pain, technical accuracy and number of found/missed pathologies as well as average time for successful endoscopy will be recorded. After one month or 50 supervised, self performed endoscopies, trainees will be evaluated again with the above mentioned criteria during ten consecutive investigations.

Interventions

3 weeks/2 hours per day of structured training for a total of 20 hours on the virtual endoscopy simulator with the GI-Mentor Virtual simulator device

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Trainees: naive to real patient endoscopy before training phase

Exclusion criteria

* Medical doctors with experience in gastrointestinal endoscopy * Patients sedated for upper GI endoscopy * Patients unwilling or unable to sign informed consent

Design outcomes

Primary

MeasureTime frame
Patient satisfaction measured on a visual analogue scale (VAS)once immediately after patient endoscopy

Secondary

MeasureTime frame
pain during endoscopy, measured with patient documentation on a visual analogue scale (VAS)once immediately after patient endoscopy
technical accuracy (oral introduction of the scope into the esophagus, ability of passing the endoscope through the pylorus, inversion of the scope in the gastric fundus)during endoscopy
number of found/missed pathologiesduring endoscopy
average time for successful endoscopyduring endoscopy

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026