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Clinical Trials/NCT00123500
NCT00123500
Completed
N/A

ACTION! Wellness Program for Elementary School Personnel

Tulane University School of Public Health and Tropical Medicine1 site in 1 country1,202 target enrollmentSeptember 2004

Overview

Phase
N/A
Intervention
Not specified
Conditions
Obesity
Sponsor
Tulane University School of Public Health and Tropical Medicine
Enrollment
1202
Locations
1
Primary Endpoint
Body mass index (BMI)
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The goal of the project is to develop, implement, and evaluate, through a randomized controlled trial at a worksite, an intervention to promote increased physical activity behavior and healthier eating behavior to reduce overweight and obesity among elementary school personnel.

Detailed Description

BACKGROUND: The dramatic increase in the prevalence of overweight and obesity among adults in the United States during the past two decades is related to increased cardiovascular disease, hypertension, dyslipidemia, diabetes, and other chronic diseases. With 63.9% of working-age adults employed, worksites are targets for prevention and intervention programs to control overweight and obesity. Worksite interventions have the potential to reach a large number of individuals in a common and shared environment. DESIGN NARRATIVE: This is a group-randomized trial involving 20 elementary schools in Jefferson Parish public schools. Schools will be the unit of randomization; 10 schools will be randomly allocated to implement the intervention, and 10 schools will serve as controls. The primary aim of the program is to reduce mean body weight. Secondary aims relate to changes at both the individual level and the environmental level. The intervention will address the two major determinants of overweight and obesity: physical activity and diet. A School Wellness Committee at each site will be instrumental in identifying and implementing components of the intervention.

Registry
clinicaltrials.gov
Start Date
September 2004
End Date
August 2009
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Tulane University School of Public Health and Tropical Medicine
Responsible Party
Principal Investigator
Principal Investigator

Larry S. Webber

Professor

Tulane University School of Public Health and Tropical Medicine

Eligibility Criteria

Inclusion Criteria

  • Healthy adults with no contraindications to participating in an intervention to improve eating and exercise behaviors
  • Healthy adults with no contraindications to participating in any of the measurement procedures

Exclusion Criteria

  • Inability to participate in routine physical activity

Outcomes

Primary Outcomes

Body mass index (BMI)

Time Frame: Measured at the end of the second year of intervention

Secondary Outcomes

  • 24-hour dietary recall(Measured at baseline (Fall 2006) and follow-up (Fall 2008))

Study Sites (1)

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