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Clinical Trials/NCT02361463
NCT02361463
Completed
Not Applicable

2D Versus 3D Laparoscopic Training on a Virtual Reality Simulator - A Randomised Trial

Rigshospitalet, Denmark1 site in 1 country32 target enrollmentFebruary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stereoscopic Vision
Sponsor
Rigshospitalet, Denmark
Enrollment
32
Locations
1
Primary Endpoint
Time (minutes) to reach the predefined proficiency level for the basic skills and the salpingectomy procedure
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Laparoscopy training programs with virtual reality simulators are widely used before new surgeons are allowed to operate on patients. Laparoscopic surgery results in shorter time to recover, less surgical trauma and thereby a shorter stay at the hospital compared with open surgery. However, it is more difficult to learn laparoscopic surgery, than open surgery, in part because surgeons have to work in a 3-dimensional space, through a 2-dimensional interface on a screen. This results in loss of depth perception and therefore a higher visual and cognitive load. This trial examines if using 3D vision instead of 2D vision on the laparoscopic virtual reality simulator reduces the time to reach proficiency, by decreasing the cognitive and visual load during practice on a Virtual Reality Simulator.

Registry
clinicaltrials.gov
Start Date
February 2015
End Date
August 2015
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stine Maya Dreier Sørensen

Master student / B.M.Sc.

Rigshospitalet, Denmark

Eligibility Criteria

Inclusion Criteria

  • Residents working in Denmark. Participants are required to have a medical license and provide informed consent before inclusion

Exclusion Criteria

  • Participation in prior studies involving laparoscopic training.
  • Experience with laparoscopy surgery (having performed minimum one laparoscopic procedure as primary surgeon, including supervised procedures).
  • Performing more than 3 supervised laparoscopy surgeries during the intervention.
  • Performing laparoscopy surgery between the intervention and the retention test 3-6 weeks after.
  • No informed consent.
  • Does not speak Danish on a conversational level.

Outcomes

Primary Outcomes

Time (minutes) to reach the predefined proficiency level for the basic skills and the salpingectomy procedure

Time Frame: 1 year

Secondary Outcomes

  • Time (minutes) to reach the predefined proficiency level for the basic skills and salpingectomy procedure under 2D conditions after 3-6 weeks without laparoscopic training during the follow-up period(1 year)

Study Sites (1)

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