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OpenTrials
Completed

NCT Number: NCT00824486

Home Safety Intervention Using a Safe Home Model

This project seeks to determine the efficacy of safety education using a safe home model. The 4 X 8 ft. model is designed to look like a house; each of 4 "rooms" has a focused safety message. Families will be enrolled in the clinic and randomized to one of two groups, the safe home model group and the printed safety education materials (TIPP materials) group. The investigators will compare the retention of safety information among caregivers instructed using these two methods. The hypothesis is that families in the safe home model group will have improved retention of safety information.

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Key information

Conditions

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's Memorial Hospital

Chicago, Illinois, 60614, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Caregivers of children younger than 6 years old

Exclusion criteria

  • Language other than English or Spanish

Treatment and study plan

Injury prevention education (TIPP)

Behavioral

using TIPP materials

Injury prevention education (safe home)

Behavioral

using safe home model

Sponsors and collaborators

Lead sponsor

Ann & Robert H Lurie Children's Hospital of Chicago

Other

Registry information

Official study title

A Randomized Trial of a Home Safety Intervention Using a Safe Home Model

Important dates

Study start
2003
Study completion
2007
First posted
Jan 16, 2009
Registry last updated
Jan 16, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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