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The Seatbelt Intervention Study

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University of Michigan

Status

Completed

Conditions

High Risk Population of Part-time Seatbelt Users

Treatments

Other: Interactive interview and tailored family centered seatbelt safety intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02258633
HUM00026025

Details and patient eligibility

About

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.

Enrollment

200 patients

Sex

All

Ages

7 to 14 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

Intervener Brief Intervention (IBI)
Experimental group
Description:
Subjects and parents will complete a Brief Motivational Interview (BMI) incorporating personalized feedback, discussion of choices and changes, and therapist led intervention message relating behavioral change and future goals.
Treatment:
Other: Interactive interview and tailored family centered seatbelt safety intervention
Enhanced Usual Care
No Intervention group
Description:
Subjects and parents will receive standard trauma care, plus complete brief questionnaires and receive general safety information.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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