Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
79 participants
INTERVENTIONAL
2006-05-31
2008-07-31
Brief Summary
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Detailed Description
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We propose a 1 year randomized controlled trial comparing weight changes among low-income, overweight children randomized to participate in an after school team sports program versus a traditional weight control/health education program.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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After school sports
After school team sports
After school team sports program
Health and Nutrition Education
Health and Nutrition Education Active Placebo Control
After school health education program
Interventions
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After school team sports program
After school health education program
Eligibility Criteria
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Inclusion Criteria
* 8-11.9 years old
* BMI \>= 85th percentile for age and sex on the 2000 Centers for Disease Control (CDC) growth charts
* Clearance to participate from medical care provider
* Willing, able, and available to attend an after school program
* Not planning to move from school district within the next 12 months
* Speaks and reads English or Spanish
* Child has not repeated more than one grade in school
* Completion of signed active informed consent (parent or guardian) and assent (child) to participate, which includes a description of the two interventions and requires their willingness to be randomized.
Exclusion Criteria
* Have a condition that limits their participation in physical activity enough that they are not able to participate in Physical Education at school (e.g. significant structural heart disease)
* Have been diagnosed with a chronic illness that affects their growth and/or weight (e.g. type 1 diabetes, hypothyroidism, inflammatory bowel disease)
* Have taken systemic steroids (oral, intravenous, or intramuscular) for a period of more than 21 days in the past year
* Are taking other medications affecting their growth and/or weight \[e.g. methylphenidate hydrochloride (HCL)\]
* Are pregnant
* Are unable to complete the informed consent process
8 Years
11 Years
ALL
Yes
Sponsors
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
Stanford University
OTHER
Responsible Party
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Principal Investigators
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Thomas N Robinson, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Dana L Weintraub, MD
Role: STUDY_DIRECTOR
Stanford University
Locations
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Stanford Prevention Research Center
Palo Alto, California, United States
Countries
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Other Identifiers
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31487
Identifier Type: -
Identifier Source: org_study_id