Brief Child Safety Interventions in Emergency Departments (Safety in Seconds)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Wendy Shields, Johns Hopkins Bloomberg School of Public Health
ClinicalTrials.gov Identifier:
NCT01432041
First received: September 8, 2011
Last updated: September 9, 2011
Last verified: September 2011
  Purpose

Safety in seconds is a randomized controlled trial of a computer tailored Injury Prevention program which was conducted in the waiting area of a level 1 pediatric trauma center. A computer kiosk was used to randomly assign participants to study groups, collect baseline data and generate tailored reports based on responses to assessment items. An intervention group received a personalized and stage-tailored safety report and a control group received a personalized, but otherwise generic report on other child health topics. Telephone follow-up interviews were conducted 2-4 weeks and again 4-6 months after enrollment. Home visits were completed for a subset (n=100) of parents who completed the 4-6 month follow-up interview. The study aimed to increase knowledge, self reported and observed safety behaviors.


Condition Intervention
Injury Prevention
Behavioral: tailored health education

Study Type: Interventional
Study Design: Primary Purpose: Prevention
Official Title: Brief Child Safety Interventions in Emergency Departments (Safety in Seconds)

Resource links provided by NLM:


Further study details as provided by Johns Hopkins Bloomberg School of Public Health:

Primary Outcome Measures:
  • Knowledge outcome [ Designated as safety issue: No ]
    Measures of Home safety Knowledge

  • Reported and Observed Home Safety behaviors [ Designated as safety issue: No ]
    Reportedf and Observed Home Safety Behaviors (Car Seats, Smoke Alarms)


Enrollment: 901
Study Start Date: September 2004
Study Completion Date: December 2005
Primary Completion Date: December 2005 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: tailored health education
    Health Information via a computer kiosk in the pediatric emergency department
    Other Name: Tailored health Communication
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Eligible parents or guardians had to be English-speaking;
  • have a child between 4-66 months of age seeking treatment for an injury or medical complaint, or have an age-appropriate sibling of a child being seen for these reasons;
  • live in Baltimore City;
  • and live with the child at least some of the time.

Exclusion Criteria:

-parents which did not meet inclusion criteria

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01432041

Sponsors and Collaborators
Johns Hopkins Bloomberg School of Public Health
Investigators
Principal Investigator: Andrea C Gielen, ScD Johns Hopkins School of Public Health
  More Information

Publications:
Responsible Party: Wendy Shields, Research Associate, Johns Hopkins Bloomberg School of Public Health
ClinicalTrials.gov Identifier: NCT01432041     History of Changes
Other Study ID Numbers: JHSPH-H.31.02.04.03.B2
Study First Received: September 8, 2011
Last Updated: September 9, 2011
Health Authority: Johns Hopkins Institutional Review Board USA:

Keywords provided by Johns Hopkins Bloomberg School of Public Health:
Injury prevention
smoke alarms
car seats

ClinicalTrials.gov processed this record on September 16, 2014