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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
  Purpose
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.

Condition Intervention
Surgical Proficiency Behavioral: Simuvision Simulator

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Collaborative Surgical Proficiency Initiative

Further study details as provided by Phoenix Integrated Surgical Residency:

Estimated Enrollment: 90
Study Start Date: June 2007
Estimated Study Completion Date: March 2011
Estimated Primary Completion Date: March 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Surgical resident or attending Behavioral: Simuvision Simulator
Participants will perform common surgical procedures on the simulator

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   23 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Surgical residents and attendings from Banner Good Samaritan Medical Center
Criteria

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:

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01050335


Locations
United States, Arizona
Simulation and Education Training (SimET) Center, Banner Good Samaritan Medical Center
Phoenix, Arizona, United States, 85006
Sponsors and Collaborators
Phoenix Integrated Surgical Residency
Investigators
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
  More Information

Responsible Party: Kanav Kahol, PhD Principal Investigator, Simulation and Education Training (SimET) Center, Banner Good Samaritan Medical Center
ClinicalTrials.gov Identifier: NCT01050335     History of Changes
Other Study ID Numbers: 01-07-0044
First Submitted: January 14, 2010
First Posted: January 15, 2010
Last Update Posted: January 15, 2010
Last Verified: June 2009