Traditional Versus Virtual Reality for Surgical Skills for ObGyn Residents (SIMUTEC)
|ClinicalTrials.gov Identifier: NCT03395821|
Recruitment Status : Unknown
Verified December 2017 by Ricardo Francalacci Savaris, Hospital de Clinicas de Porto Alegre.
Recruitment status was: Recruiting
First Posted : January 10, 2018
Last Update Posted : January 10, 2018
|Condition or disease||Intervention/treatment||Phase|
|Gynecologic Disease||Behavioral: Conventional training Behavioral: Virtual Reality+conventional training||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||24 participants|
|Intervention Model:||Parallel Assignment|
|Intervention Model Description:||Two groups will be compared according to their surgical skills.|
|Masking:||None (Open Label)|
|Official Title:||Comparison Between Exclusive Surgical Training Versus Virtual Reality Plus Traditional Training in Surgical Skills of Residents of Obstetrics and Gynecology|
|Actual Study Start Date :||December 22, 2017|
|Estimated Primary Completion Date :||December 1, 2018|
|Estimated Study Completion Date :||December 1, 2018|
Active Comparator: Conventional training
Residents will receive the traditional training for laparoscopic surgery according to their residency program.
Behavioral: Conventional training
traditional training according to residency program
Experimental: Virtual Reality+conventional training
Residents will receive 12 weeks of virtual training for laparoscopy and their traditional training for laparoscopic surgery according to their residency program.
Behavioral: Virtual Reality+conventional training
virtual reality training+traditional training using virtual reality
- Efficiency of technical skills (%) [ Time Frame: 12 weeks ]The software analyzes the percentage of time the needle-holders' ends are kept outside the operative field (%); total number of entrance and exit points through which the needle has passed; total aggressive tissue handling; total amount of strain applied to tissue during needle passages; total needle loading time; total number of completed knots; total number of needle loadings; total number of needle passages; total number of stitches; total time the needle-holders' ends are kept outside the predefined operative field; total time to accomplish the suture; Total time to form a knot. For salpingectomy: efficiency of cautery (%); number of non-cauterized bleeding; number of serious complications: possible damage to vital structures; safe cautery (%); the time cautery is applied without appropriate contact with adhesions; total number of applied clips.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03395821
|Contact: Guilherme G Pretto, MD,PhD||+1(51)email@example.com|
|Contact: Ricardo F Savaris, MD,PhD||+1(51)firstname.lastname@example.org|
|Porto Alegre, RS, Brazil, 90035-903|
|Contact: RICARDO F SAVARIS, MD,PHD email@example.com|
|Study Chair:||Leandro T Cavazzola, MD,PhD||Hospital de Clínicas de Porto Alegre|