NCT00824486

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
Completed

Started Jun 2003

Longer than P75 for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2003

Completed
3.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2007

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

January 15, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 16, 2009

Completed
Last Updated

January 16, 2009

Status Verified

January 1, 2009

First QC Date

January 15, 2009

Last Update Submit

January 15, 2009

Conditions

Keywords

childinjury prevention

Study Arms (2)

TIPP

ACTIVE COMPARATOR

Injury prevention education using TIPP materials

Behavioral: Injury prevention education (TIPP)

Safe Home Model

EXPERIMENTAL

Injury prevention education using safe home model

Behavioral: Injury prevention education (safe home)

Interventions

using TIPP materials

TIPP

using safe home model

Safe Home Model

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Caregivers of children younger than 6 years old

You may not qualify if:

  • Language other than English or Spanish

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Children's Memorial Hospital

Chicago, Illinois, 60614, United States

Location

MeSH Terms

Interventions

tyrosyl-1,2,3,4-tetrahydro-3-isoquinolinecarbonyl-phenylalanyl-phenylalanine

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 15, 2009

First Posted

January 16, 2009

Study Start

June 1, 2003

Study Completion

March 1, 2007

Last Updated

January 16, 2009

Record last verified: 2009-01

Locations