Medical Residents Performance: Effect of Simulation-Based Training
This study has been completed.
Sponsor:
St. Luke's-Roosevelt Hospital Center
Information provided by (Responsible Party):
St. Luke's-Roosevelt Hospital Center
ClinicalTrials.gov Identifier:
NCT00612131
First received: January 28, 2008
Last updated: October 15, 2012
Last verified: September 2007
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Purpose
I Hypothesis:
- Simulation-based training in maximal barrier precaution technique during central venous catheter (CVC) placement is superior to general videotape-based training
- Baseline performance in maximal barrier precaution technique of PGY 2 and 3 Medical residents, certified in CVC placement, is poor
- PGY 2 and 3 medical residents have low self-perceived confidence in mastering maximal barrier precaution technique during central venous catheter (CVC) placement
- PGY 2 and 3 medical residents undergoing simulation-based training in maximal barrier precaution technique during central venous catheter (CVC) placement have good recall after 3 months
| Condition |
|---|
|
Healthy |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Medical Residents Performance in Maximum Barrier Precautions During Central Venous Catheter Placement: Effect of Simulation-Based Training |
Further study details as provided by St. Luke's-Roosevelt Hospital Center:
Primary Outcome Measures:
- -Primary outcome: Medical residents' performance in maximal barrier precaution (MBP) technique during central venous catheter (CVC) placement [ Time Frame: 2 weeks ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Secondary outcome: Medical residents' confidence level in maximal barrier precaution (MBP) technique during CVC placement [ Time Frame: 1 week ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 47 |
| Study Start Date: | November 2007 |
| Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
Show Detailed Description
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
MEDICAL RESIDENTS
Criteria
Inclusion Criteria:
- Medical residents who completed one year training in internal medicine program who are certified by their program to place and supervise medical interns in placement of CVC
Exclusion Criteria:
- Refusal to participate in the study
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00612131
Locations
| United States, New York | |
| St. Luke's Roosevelt Hospital | |
| New York, New York, United States, 10019 | |
Sponsors and Collaborators
St. Luke's-Roosevelt Hospital Center
Investigators
| Principal Investigator: | Hassan Khouli | St. Luke's-Roosevelt Hospital Center |
More Information
No publications provided by St. Luke's-Roosevelt Hospital Center
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | St. Luke's-Roosevelt Hospital Center |
| ClinicalTrials.gov Identifier: | NCT00612131 History of Changes |
| Other Study ID Numbers: | 07-125 |
| Study First Received: | January 28, 2008 |
| Last Updated: | October 15, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by St. Luke's-Roosevelt Hospital Center:
|
medical residents PGY 2 and 3 |
ClinicalTrials.gov processed this record on June 18, 2013