Patient Outcomes in Simulation Education (POISE) Intravenous (IV) and Lumbar Puncture (LP) Multi-institution Protocol
Sponsor
Columbia University (Other)
Overall Status
Completed
CT.gov ID
NCT01548547
Collaborator
(none)
210
1
2
9
23.4
Study Details
Study Description
Brief Summary
This study aims to compare the clinical efficacy of multimedia audiovisual training to hands on "practice till perfect" training for pediatric and emergency medicine residents' procedural skills. This initial study will explore the success rates on infant lumbar puncture and child intravenous access skills in post-graduate year one pediatric residents.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Study Design
Study Type:
Interventional
Actual Enrollment
:
210 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Official Title:
Patient Outcomes in Simulation Education (POISE) Intravenous (IV) and Lumbar Puncture (LP) Multi-institution Protocol
Study Start Date
:
Jun 1, 2008
Actual Primary Completion Date
:
Mar 1, 2009
Actual Study Completion Date
:
Mar 1, 2009
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: LP mastery learning group
|
Other: Simulation-based mastery learning
Hands-on coached deliberate practice on a simulator. Training until mastery achieved.
|
Active Comparator: IV mastery learning group
|
Other: Simulation-based mastery learning
Hands-on coached deliberate practice on a simulator. Training until mastery achieved.
|
Outcome Measures
Primary Outcome Measures
- Rate of clinical success with lumbar puncture (LP) procedures [Up to one year]
Online performance form
- Rate of clinical success with intravenous (IV) procedures [Up to one year]
Online performance form
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- Pediatric interns at POISE network hospitals
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Columbia University | NY | New York | United States | 10032 |
Sponsors and Collaborators
- Columbia University
Investigators
- Principal Investigator: David Kessler, MD, MSc, Columbia University
- Study Director: Martin Pusic, MD, PhD, Columbia University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Martin V. Pusic,
Adjunct Assistant Clinical Professor of Pediatrics,
Columbia University
ClinicalTrials.gov Identifier:
NCT01548547
Other Study ID Numbers:
- AAAE0924
First Posted:
Mar 8, 2012
Last Update Posted:
Mar 8, 2012
Last Verified:
Mar 1, 2012
Keywords provided by Martin V. Pusic,
Adjunct Assistant Clinical Professor of Pediatrics,
Columbia University
Additional relevant MeSH terms: