Evaluation of a Resident Curriculum in Firearm Injury Prevention
Evaluation of a Firearm Injury Prevention Web-based Curriculum
1 other identifier
interventional
92
1 country
1
Brief Summary
The purpose of this project is to evaluate the efficacy of a web-based curriculum designed to teach pediatric practitioners how to provide injury prevention anticipatory guidance, emphasizing firearm injury prevention in a clinic setting. Data will be collected regarding the curriculum's effectiveness using a web-based questionnaire which will be administered to pediatric residents prior to, immediately post, and six months following completion of the curriculum. Pre- and post-test questionnaires will be compared. Residents will also be asked to evaluate the curriculum by completing a survey. We hypothesize that the curriculum will improve residents' knowledge, attitudes and beliefs, and self-efficacy regarding firearm injury prevention anticipatory guidance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2007
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2008
CompletedFirst Submitted
Initial submission to the registry
December 4, 2009
CompletedFirst Posted
Study publicly available on registry
December 7, 2009
CompletedDecember 7, 2009
December 1, 2009
7 months
December 4, 2009
December 4, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Likert-scale based testing
pre-test, post-test, and 6-months post-test
Interventions
Firearm injury prevention anticipatory guidance curriculum
Eligibility Criteria
You may qualify if:
- Pediatric resident at Children's Memorial Hospital
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Children's Memorial Hospital
Chicago, Illinois, 60614, United States
Related Links
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Leslie M Dingeldein, MD
Ann & Robert H Lurie Children's Hospital of Chicago
- PRINCIPAL INVESTIGATOR
Karen Sheehan, MD, MPH
Ann & Robert H Lurie Children's Hospital of Chicago
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
December 4, 2009
First Posted
December 7, 2009
Study Start
December 1, 2007
Primary Completion
July 1, 2008
Study Completion
July 1, 2008
Last Updated
December 7, 2009
Record last verified: 2009-12