The Seatbelt Intervention Study

Not Applicable

Completed

• Conditions: High Risk Population of Part-time Seatbelt Users

• Registration Number: NCT02258633
• Lead Sponsor: University of Michigan

Brief Summary

The study will use a randomized controlled design testing the effectiveness of the following intervention: (i) intervener brief intervention (IBI) vs. (ii) Enhanced usual care (EUC). The study will identify children ages 2-14 at a pediatric trauma center. Children and their parents who agree to participate in the study will then complete a screening survey to identify part time seatbelt use. Those who screen positive will complete a more detailed baseline survey and then be randomized to one of two study conditions. At one month, a follow up assessment by telephone will be completed.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-03
• Primary Completion: 2010-02
• Status Verified: 2014-10
• Study First Submitted: 2014-10-02
• Study First Submitted QC: 2014-10-06
• Last Update Submitted: 2014-10-06
• Study First Posted: 2014-10-07
• Last Update Posted: 2014-10-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

• Children ages 7-14 and their parent or guardian, at a pediatric trauma center
• Child admitted to hospital with diagnosis of injury other than sexual assault and suicide
• Identify as part time seat belt users

Exclusion Criteria

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Seat belt knowledge	1 month	Follow up telephone assessment on level of knowledge of seat belt use and risk factors
Seat belt use	1 month	Follow up telephone assessment on full time seat belt use by parent and child
Attitudes	1 month	Follow up telephone assessment of positive attitude, motivation, and self-efficacy regarding safety restraint use.