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Clinical Trials/NCT00708461
NCT00708461
Completed
Not Applicable

Environmental Intervention for Weight Gain Prevention

University of Minnesota1 site in 1 country1,747 target enrollmentJanuary 2006
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
University of Minnesota
Enrollment
1747
Locations
1
Primary Endpoint
Change in Body Mass Index (BMI)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The primary aim of this research is to evaluate the efficacy of a multicomponent worksite-based, environmental intervention in reducing weight increase and obesity over time in working adults.

Detailed Description

This study is a randomized trial designed to evaluate the effectiveness of a multi-component worksite intervention with strong environmental components to prevent weight gain. Six worksites will be randomized to either an intervention or a no-treatment control group. The intervention will be comprised of 1) changing the availability, portion sizes, and prices of foods and beverages sold to employees in their worksites in ways that encourage healthier food choices; 2) increasing the availability of physical activity opportunities at the worksite by implementing walking programs and increasing stairwell access and attractiveness; 3) placing scales in the work environment to encourage body weight monitoring and to enable workers to set goals for their weight; and 4) to provide educational materials to all employees to make them aware of the environmental intervention and of behavioral practices likely to be effective in preventing weight gain. The intervention will be implemented for a 2-year period in each intervention site. Effectiveness will be evaluated by assessing body weight, eating behavior and physical activity in a cohort of employees in both control and intervention sites at baseline and again 2 years later. Weight trends in these populations will also be compared to data from national and state-level annual surveys of weight in representative population samples. Data will be collected on the effects of specific intervention components via aggregate measures of food choice and physical activity.

Registry
clinicaltrials.gov
Start Date
January 2006
End Date
March 2010
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age 18 or older
  • generally in good health
  • part- or full-time employee in one of the participating worksites

Exclusion Criteria

  • work on site \<50% of the time
  • work second or third shift

Outcomes

Primary Outcomes

Change in Body Mass Index (BMI)

Time Frame: Baseline to 24 months

Assessed in kilograms per meter squared.

Study Sites (1)

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