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Obesity Prevention in African American School Children - Article


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Clinical Trial: Obesity Prevention in African American School Children

This study is currently recruiting patients.

Sponsored by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Purpose

Obesity is the second leading preventable cause of disease and death in the United States. Low socioeconomic status (SES) and minorities are disproportionately affected. Obesity prevention among children and adolescents is a public health priority. Schools have been identified as key settings for obesity prevention; however, most health education interventions have had only a moderate effect on body weight. We propose a randomized intervention trial (pilot study) to test the feasibility and effectiveness of a school-based, environmental obesity prevention program in urban low-SES African American students. Schools, students and their families, and local communities will be involved to promote healthy eating and physical activity (HEPA) for prevention of childhood obesity. Six Chicago public schools will be randomly assigned as intervention (4 schools) and controls (2 schools). Focus group studies will assess needs and barriers for promotion of HEPA and guide the intervention. The intervention group will receive a School Environment Enrichment (SEE) program to modify the school physical and social environment, targeting food service, recess, physical education (PE) and school climate, and a Community Support & Environment Modification (CSEM) program, involving local corner and chain grocery stores to promote healthy eating among students and their families. Family involvement will be included for 5th and 6th graders, who will be followed for two years, to test ways to modify family environment. To assess the intervention effectiveness, multilevel data will be collected from schools (eg, food service, recess and PE), students (eg, body weight, eating and physical activity), parents (eg, family food purchasing practices) and communities (eg, available choices of snack foods in local stores). In addition, process evaluation data will be collected to assess the feasibility and acceptance (participation and satisfaction) of various intervention components by the target audience. The primary outcome variable is change in students’ body weight status; secondary outcomes include changes in students’ eating behavior and physical activity and changes in target environmental factors. In addition, cost-effectiveness of the intervention will be determined. If the intervention proves effective, a full-scale study will be developed. Findings from this study will provide insights into the prevention of obesity among low-SES and minority students.

Condition Treatment or Intervention
Obesity
 Behavior: School + family changes promoting healthy eating + activity

MedlinePlus related topics:  Obesity

Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study

Further Study Details: 

Expected Total Enrollment:  900

Study start: February 2003

Eligibility

Ages Eligible for Study:  8 Years and above,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

All 4-6th graders in the selected public schools in Chicago and their parents/guardians

Location and Contact Information

Youfa Wang, PhD, MD      312 355 3382    youfwang@uic.edu
Lisa Tussing, MS      312 996 0995    ltussing@uic.edu

Illinois
      University of Illinois at Chicago, Department of Human Nutrition, Chicago,  Illinois,  60612,  United States; Recruiting
Youfa Wang, PhD, MD  312-355-3382    youfwang@uic.edu 
Lisa Tussing, MS  312 996 0995    ltussing@uic.edu 

Study chairs or principal investigators

Youfa Wang, PhD, MD,  University of Illinois at Chicago, Department of Human Nutrition   

More Information

Study ID Numbers:  OPAASC
Record last reviewed:  December 2004
Last Updated:  December 15, 2004
Record first received:  May 21, 2003
ClinicalTrials.gov Identifier:  NCT00061165
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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