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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05834504
Other study ID # DPiLS trial
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 29, 2022
Est. completion date March 26, 2023

Study information

Verified date April 2023
Source Copenhagen Academy for Medical Education and Simulation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this trial is to investigate if short intervals (1-2 days) between training sessions are more efficient than practicing with longer intervals (6-8 days) between sessions during proficiency-based laparoscopic simulator training. Our hypothesis is that just 1-2 days of break between sessions is optimal for the acquisition of laparoscopic skills and that a shorter interval between sessions is optimal for training.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date March 26, 2023
Est. primary completion date March 26, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Master's degree medical students, enrolled at a Danish University. Exclusion Criteria: - Medical students that have participated in prior studies or similar involving laparoscopic training. - Performing laparoscopy surgery between the intervention and the retention test 3-5 weeks after. - No informed consent. - Does not speak Danish on a conversational level. - Any disability or injury regarding eyesight and mobility.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Short distributed training (1-2 days)
The intervention group will practice four basic skills and one procedural module on the Laparoscopic "Lapsim" Virtual Reality Simulator. They will practice with 1-2 days of break in between training sessions until proficiency level is achieved.

Locations

Country Name City State
Denmark Copenhagen Academy For Medical Education and Simulation (Cames) Copenhagen Capital Region

Sponsors (1)

Lead Sponsor Collaborator
Copenhagen Academy for Medical Education and Simulation

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to proficiency The total effective training time (minutes) to reach the predefined proficiency level for both the four basic skills and the salpingectomy module. 6 months
Secondary Retention test The total effective training time (minutes) to reach the predefined proficiency level for both the four basic skills and the salpingectomy module after 3-5 weeks without laparoscopic training from the last training session. 6 months
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