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Wellness Program for Elementary School Personnel

ACTION! Wellness Program for Elementary School Personnel

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00123500
Enrollment
1202
Registered
2005-07-25
Start date
2004-09-30
Completion date
2009-08-31
Last updated
2017-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Obesity

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.

Interventions

BEHAVIORALDiet

Diet

BEHAVIORALPhysical Activity

Physical Activity

BEHAVIORALEnvironment

Environment

OTHERControl Group

Control Group

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
Tulane University School of Public Health and Tropical Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Body mass index (BMI)Measured at the end of the second year of intervention

Secondary

MeasureTime frame
24-hour dietary recallMeasured at baseline (Fall 2006) and follow-up (Fall 2008)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026