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A Pilot Study on Training Simulator Efficacy

Training Simulator Efficacy in Developing Thoracic and General Surgical Skills in an Academic Residency Program: a Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05436899
Enrollment
36
Registered
2022-06-29
Start date
2022-09-01
Completion date
2025-12-31
Last updated
2023-08-22

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

Conditions

Laparoscopic Surgery, Medical Education, Simulation Training

Keywords

Education, Simulation, Virtual reality, Laparoscopic surgery, Learning curve, Endoscopic surgery, Thoracoscopic surgery

Brief summary

The purpose of this study is to plan an effective learning path in minimally invasive thoracic and general surgery with a virtual training simulator for trainees and to assess the improvement of residents' surgical skills by the introduction of this virtual training program.

Detailed description

All thoracic and general surgery trainees at the first and second year of residency will be randomized in two groups: A) trainees undergoing an intensive (twice a week) virtual training program and B) those undergoing a non-intensive virtual training program (once a week). The virtual training program will be organized in 4 modules, each of 12 weeks and, according to the training simulator instructions, for each surgical skill there are predetermined goals to be achieved by the trainee. Data about duration of surgical maneuvers and type and number of mistakes made by the trainee at each training session will be collected and compared with those of the same trainee at the previous session; this will assess the number of training sessions required to achieve the training simulator predetermined goals. Moreover, the same data will be registered at the beginning and at the end of each courses to compare the two groups of trainees (intensive vs non-intensive program).

Interventions

Complete 4 courses, each of 12 weeks, of virtual reality simulation on LapSim surgical simulator.

OTHERLapSim exam

Completed at the beginning and at the end of each of the 4 courses the corresponding exam task.

Sponsors

Università degli Studi dell'Insubria
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
24 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Trainees at the first and second year of residency in thoracic or general surgery

Exclusion criteria

* Fully trained surgeons * Persons who are not trainees at year of specialization higher than the second

Design outcomes

Primary

MeasureTime frameDescription
Learning curves of time, errors and economy of motion for each training tasks48 weeksFor each task, the computer automatically measures set parameters. Time, errors and economy of motion will be used in data analysis to create the learning curves for both intensive and non-intensive training group.

Secondary

MeasureTime frameDescription
Intensive vs non-intensive training group48 weeksFor each exam tasks of the four training courses, compare the difference between the intensive and non-intensive training group, before and after each program training. Time, errors and economy of motion will be used in data analysis.

Countries

Italy

Contacts

Primary ContactAndrea Imperatori
andrea.imperatori@uninsubria.it+39-0332-393195

Outcome results

None listed

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