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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02069951
Other study ID # 102169
Secondary ID
Status Completed
Phase N/A
First received February 20, 2014
Last updated May 9, 2015
Start date February 2014
Est. completion date September 2014

Study information

Verified date May 2015
Source Rigshospitalet, Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

Surgical training programs using virtual reality simulators often only use basic skills training and the use of procedural training is very limited. Procedural training differs from basic skills training by requiring integration of isolated skills and decision making and planning components. However, it is unknown if it is necessary to practice all procedures before operating on actual patients or whether it is simply a matter of learning psychomotor skills and if these skills are transferable between different tasks.

The main hypothesis is that practicing a laparoscopic procedure on a simulator makes it easier to reach proficiency on a different laparoscopic procedure on the simulator because participants have already practiced the integration of isolated skills.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Medical students enrolled at The Faculty of Health Science, University of Copenhagen.

- Obtained the bachelor degree in medicine.

- Signed informed consent.

Exclusion Criteria:

- Previous participation in trials involving laparoscopic training.

- Experience with laparoscopy surgery (having performed minimum one laparoscopic procedure as primary surgeon, including supervised procedures).

- No informed consent.

- Does not speak Danish on a conversational level.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
Practice a procedural module on a simulator


Locations

Country Name City State
Denmark Rigshospitalet Copenhagen

Sponsors (2)

Lead Sponsor Collaborator
Rigshospitalet, Denmark Copenhagen University Hospital, Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Subjective Mental Effort Question score after the 1st repetition To score the level of stress, all the participants will be required to the Subjective Mental Effort Questionnaire after the first repetition of a procedural module. The SMEQ is a cognitive workload questionnaire with a scale of 0 to 150 points Up to 26 weeks No
Other Motor skills performance parameters The total path length (cumulative distance tip movement for both the right and left instrument) for the first attempt on procedural module B will be compared for the intervention and the control group.
The total angular path (cumulative angular degrees for both the right and left instrument) for the first attempt on procedural module B will be compared for the intervention and the control group.
The total procedure time for the first attempt on procedural module B will be compared for the intervention and the control group.
Up to 26 weeks No
Primary The number of repetitions needed to reach a predefined proficiency level for a procedural module on a simulator The number of repetitions needed to reach a predefined proficiency level for a procedural module (a laparoscopic salpingectomy) on the simulator. Up to 26 weeks No
Secondary The effective training time on the simulator (minutes) needed to reach the predefined proficiency level for a procedural module. The effective training time on the simulator (minutes) needed to reach a predefined proficiency level for a procedural module (a laparoscopic salpingectomy) on the simulator. Up to 26 weeks No
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