- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00982917
Stamp-in-Safety Playground Safety Project
September 22, 2009 updated by: Ann & Robert H Lurie Children's Hospital of Chicago
Playground injuries are common at childcare centers.
Adequate adult supervision is an important component to reducing playground injuries in preschool children.
The investigators studied the Stamp-in-Safety Program, an intervention to improve adult supervision and reduce children's risky playground behaviors.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Using a non-equivalent control group design, we evaluated the Stamp-in-Safety program which increases the quality of adult supervision and rewards children for safe play.
In an urban childcare center, 71 children, ages 3-5 years, and 15 teachers participated in the study.
The primary outcome measures were teacher verbalizations (warnings, explanations, redirects), teacher location (core, outskirts, or fringe of playground), risk taking behaviors by children (using equipment appropriately), and number of injuries on the playground.
Study Type
Interventional
Enrollment (Actual)
71
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Illinois
-
Chicago, Illinois, United States, 60614
- ST. Vincent De Paul Childcare Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
3 years to 45 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- teachers at childcare center
- students at childcare center
Exclusion Criteria:
- not affiliated with childcare center
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: teachers taught curriculum
Teachers taught Stamp-in-Safety curriculum
|
30 minute curriculum on playground safety
|
|
Experimental: teachers do not learn curriculum
Teachers are not taught Stamp-in-Safety curriculum
|
30 minute curriculum on playground safety
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Improve adult supervision on playgrounds
Time Frame: 5 weeks
|
5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Decrease preschool children's risky behaviors on playgrounds
Time Frame: 5 weeks
|
5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Karen Sheehan, MD, MPH, Ann & Robert H Lurie Children's hospital of Chicago
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2006
Primary Completion (Actual)
August 1, 2006
Study Completion (Actual)
August 1, 2006
Study Registration Dates
First Submitted
September 22, 2009
First Submitted That Met QC Criteria
September 22, 2009
First Posted (Estimate)
September 23, 2009
Study Record Updates
Last Update Posted (Estimate)
September 23, 2009
Last Update Submitted That Met QC Criteria
September 22, 2009
Last Verified
September 1, 2009
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2006-12867
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.