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
  • Other: Simulation-based mastery learning
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

  1. Rate of clinical success with lumbar puncture (LP) procedures [Up to one year]

    Online performance form

  2. 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:

Study Results

No Results Posted as of Mar 8, 2012