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Clinical Trials/NCT03758586
NCT03758586CompletedNot Applicable

An Efficient Single-Session Spatial Skill Trainer for Robot-assisted Surgery: A Randomized Trial

Rambam Health Care Campus1 site in 1 country40 target enrollmentStarted: January 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Tissue piercing

Study Overview

Brief Summary

Surgical residents from a single tertiary medical center were divided into 2 groups. All residents performed 2 tasks on a Da Vinci robotic simulator system after which they were either given a real training session in spatial skills (study group) or shown a short presentation regarding robotic surgery. After training/watching the presentation, they repeated the for mentioned tasks on the robotic simulator. Improvement in surgeon performance, especially regarding tissue damage was documented.

Detailed Description

Importance: Robot-assisted surgery is becoming the mainstay of modern surgery. Efficient training techniques are essential for enhanced performance. Optimal performance during a surgical task is key to successful surgery and minimal adverse events.

Objective

To introduce and examine a single session of spatial skill training as an efficient means of improving surgical suturing performance in robot-assisted surgery.

Design: Forty-one surgical residents will be randomly assigned to training and control conditions. (1) participants will perform two da-Vinci skills simulator (dVSS) tasks to determine baseline performance. (2) the training group will undergo computer-based simulator training of spatial skills while the control group will engage in a neutral activity. (3) two dVSS tasks will be performed within 2 days of training completion to evaluate post-training performance. The experiment will be conducted until December 2018.

Participants: A convenience sample comprised of 41 surgical residents with non-robotic surgical suturing skills.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
25 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Surgical Residents with no previous robotic surgery experience.

Exclusion Criteria

  • •Non surgical residents.

Arms & Interventions

Study group

Active Comparator

Surgical residents undergoing spatial skill training.

Intervention: Computerized spatial skill training (Other)

Control group

Sham Comparator

Surgical residents not undergoing spatial skill training.

Intervention: Watching a presentation regarding robotic surgery (Other)

Outcomes

Primary Outcomes

Tissue piercing

Time Frame: up to 2 hours from enrollment

Number of times tissue was pierced during suturing

Tissue tearing

Time Frame: up to 2 hours from enrollment

Number of times tissue was teared during suturing

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

ROY LAUTERBACH MD

Principal Investigator

Rambam Health Care Campus

Study Sites (1)

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