We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Collaborative Surgical Proficiency Initiative

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified June 2009 by Phoenix Integrated Surgical Residency.
Recruitment status was:  Enrolling by invitation
Sponsor:
ClinicalTrials.gov Identifier:
NCT01050335
First Posted: January 15, 2010
Last Update Posted: January 15, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Phoenix Integrated Surgical Residency
January 14, 2010
January 15, 2010
January 15, 2010
June 2007
March 2011   (Final data collection date for primary outcome measure)
Not Provided
Not Provided
No Changes Posted
Not Provided
Not Provided
Not Provided
Not Provided
 
Collaborative Surgical Proficiency Initiative
Collaborative Surgical Proficiency Initiative
The purpose of this study is to provide a quantitative base line comparison to determine a surgeon's proficiency based on that surgeon's hand and tool movements while performing simulation tasks.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample
Surgical residents and attendings from Banner Good Samaritan Medical Center
Surgical Proficiency
Behavioral: Simuvision Simulator
Participants will perform common surgical procedures on the simulator
Surgical resident or attending
Intervention: Behavioral: Simuvision Simulator
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
90
March 2011
March 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Surgical residents and attendings from Banner Good Samaritan Medical Center
  • Range in age from 23-65 years
  • Willing to provide informed consent

Exclusion Criteria:

Sexes Eligible for Study: All
23 Years to 65 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01050335
01-07-0044
No
Not Provided
Not Provided
Kanav Kahol, PhD Principal Investigator, Simulation and Education Training (SimET) Center, Banner Good Samaritan Medical Center
Phoenix Integrated Surgical Residency
Not Provided
Principal Investigator: Kanav Kahol, PhD Simulation and Education Training (SimET) Center, Banner Good Samaritan Medical Center
Study Director: John Ferrara, MD Phoenix Integrated Surgical Residency
Phoenix Integrated Surgical Residency
June 2009