- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00142012
School-Based Obesity Prevention Program
November 16, 2005 updated by: Centers for Disease Control and Prevention
The overarching goal of this initiative is to reduce the prevalence and occurrence of obesity and increase the remission of obesity in children and adolescents through implementation of a Comprehensive School Nutrition Policy designed to promote changes in the school environment that will reinforce students' development of healthy eating and physical activity patterns inside and outside of school.
Study Overview
Detailed Description
The proposed research aims to evaluate the effects of a school-based nutrition policy initiative on prevalence, incidence and remission of overweight (BMI > 95th percentile).
It is a partnership between the Food Trust, the School District of Philadelphia and the University of Pennsylvania.
Participants are approximately 1500 students from ten schools in grades four through eight.
Half of the schools were randomized to a comprehensive School Nutrition Policy Initiative (SNPI) based on CDC's Guidelines to Promote Lifelong Healthy Eating.
The SNPI is a community-based intervention administered by the Comprehensive School Nutrition Policy Task Force that is comprised of 40 individuals representing the public and private sectors.
The goal of the SNPI is to change the school environment to: support healthy eating, increase physical activity, and decrease the prevalence of childhood overweight and diet-related diseases.
The remaining study participants are in five control schools, matched for ethnicity, SES, and type of food service.
Most students are African American and qualify for free and reduced meals at school (household income < 185% of the poverty level adjusted for household size).
Assessments of weight, height, intake, activity, inactivity and eating disorder symptomatology are being conducted at baseline and 1 and 2 years.
Study Type
Interventional
Enrollment
1500
Phase
- Not Applicable
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
8 years to 14 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Any child in 4th, 5th, 6th grades in study site schools
Exclusion Criteria:
- Any child not in 4th, 5th, 6th in study site schools
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: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
|---|
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Weightloss
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Weight maintenance
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Secondary Outcome Measures
Outcome Measure |
|---|
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Risk for overweight status (BMI 85th to 95th percentile)
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BMI z-scores, calculated for a given age and gender, will show a greater decline in intervention subjects versus controls
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Gary D. Foster, PhD, U. of Pennsylvania
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
October 1, 2002
Study Completion
June 1, 2005
Study Registration Dates
First Submitted
August 31, 2005
First Submitted That Met QC Criteria
September 1, 2005
First Posted (Estimate)
September 2, 2005
Study Record Updates
Last Update Posted (Estimate)
November 17, 2005
Last Update Submitted That Met QC Criteria
November 16, 2005
Last Verified
September 1, 2005
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CDC-OPHR-321534
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.
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