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NCT01027104 Clinical Trial

Evaluation of a Resident Curriculum in Firearm Injury Prevention

Training Clinical Trial

Official title:
Evaluation of a Firearm Injury Prevention Web-based Curriculum

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01027104
Other study ID # 2008-13313
Secondary ID
Status Completed
Phase N/A
First received December 4, 2009
Last updated December 4, 2009
Start date December 2007
Est. completion date July 2008

Study information
Verified date December 2009
Source Ann & Robert H Lurie Children's Hospital of Chicago
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 92
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Pediatric resident at Children's Memorial Hospital

Exclusion Criteria:

Study Design

Intervention Model: Parallel Assignment, Masking: Open Label

Related Conditions & MeSH terms

Intervention

Other:
• Education
Firearm injury prevention anticipatory guidance curriculum

Locations
Country Name City State
United States Children's Memorial Hospital Chicago Illinois

Sponsors (2)
Lead Sponsor Collaborator
Ann & Robert H Lurie Children's Hospital of Chicago Department of Pediatrics, Section of Emergency Medicine at Children's Mercy Hospital

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Likert-scale based testing pre-test, post-test, and 6-months post-test No
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