Status:

COMPLETED

Sports to Prevent Obesity

Lead Sponsor:

Stanford University

Collaborating Sponsors:

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Conditions:

Obesity

Eligibility:

All Genders

8-11 years

Phase:

NA

Brief Summary

The purpose of this study is to learn whether overweight children who participate in an after school team sports program improve their health as much as overweight children in a more traditional healt...

Detailed Description

There is an urgent need for feasible, effective, and cost-efficient programs to help overweight children control their weight. To start to address this unmet need, we are evaluating after school team ...

Eligibility Criteria

Inclusion

  • In the participating school district
  • 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

  • The investigators' goal is to be as inclusive as possible, however, children will not be eligible to participate if they:
  • 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

Key Trial Info

Start Date :

May 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2008

Estimated Enrollment :

79 Patients enrolled

Trial Details

Trial ID

NCT00318877

Start Date

May 1 2006

End Date

July 1 2008

Last Update

December 17 2012

Active Locations (1)

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1

Stanford Prevention Research Center

Palo Alto, California, United States, 94305