Preventing Obesity in the Worksite: A Multi-Message, Multi-"Step" Approach (Go!)

December 21, 2023 updated by: University of Minnesota
The purpose of this research study is to develop, implement, and evaluate a multi-component obesity prevention program in a workplace setting. A quasi-experimental design will be utilized, with hospital employees receiving the intervention and clinic employees serving as the comparison group. It is hypothesized that the intervention group will see greater changes in healthier eating, increased participation in physical activity, and reduced risk for obesity (weight, BMI, waist circumference).

Study Overview

Status

Completed

Conditions

Detailed Description

Over one-third of Americans are now considered obese. Efforts to prevent obesity involve changing the individual behaviors that contribute to obesity, mainly healthful eating and physical activity, as well as the social and physical context in which those behaviors take place. Due to their existing networks and available resources, worksites are a logical place to help individuals make healthy choices through health promotion efforts. The purpose of this project is to partner with a community hospital to plan, implement, and evaluate a multi-component obesity prevention program in their workplace. The prevention program will target individual and interpersonal determinants of eating behavior and physical activity, as well as the context in which these behaviors take place. This intervention will include four integrated components: (1) nutrition labeling (using stoplights, calories, and step equivalents) in the worksite cafeteria, and modifying the cafeteria environment, (2) distributing pedometers to employees, (3) persuasive media messaging, and (4) the use of "influentials" to address social norms around eating and physical activity behaviors. A quasi-experimental design will examine the effectiveness of this multi-component worksite obesity prevention program.

Study Type

Interventional

Enrollment (Actual)

499

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Minnesota
      • Duluth, Minnesota, United States, 55805
        • St. Luke's Hospital and Clinics

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Employee at one of the hospital/clinic locations participating in the study

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: weight gain prevention intervention
  1. Behavioral Approaches

    1. Distribution of pedometers
    2. Traffic light labeling in worksite cafeteria and vending machines
  2. Informational & Persuasive Messages

    1. Stair use prompts
    2. Posters, pamphlets, table toppers
    3. Website
  3. Social Approaches

    a. Identification and training of influential employees (Peer Helpers) to shape healthy norms

  4. Environmental Changes

    1. Traffic light labeling
    2. 1/2 portions at 1/2 price
    3. Walking routes
    4. Introduction of healthier foods
    5. Rearrangement of foods in the cafeteria
    6. Adjusting serving spoon size
No Intervention: No treatment comparison group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Change in Body Weight
Time Frame: Baseline, 6 months, 12 months
Baseline, 6 months, 12 months
Change in Waist Circumference
Time Frame: Baseline, 6 months,12 months
Baseline, 6 months,12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eating Behaviors
Time Frame: Baseline, 6 months, 12 months
Eating behaviors will be assessed by the Multifactor Screener (self-report questionnaire) and food purchase data (objective).
Baseline, 6 months, 12 months
Physical Activity
Time Frame: Baseline, 6 months, 12 months
Physical Activity will be assessed by multiple self-report measures (Godin Leisure Time Exercise Questionnaire, International Physical Activity Questionnaire, and questions about stair use and steps). Stair use will also be assessed by naturalistic observation.
Baseline, 6 months, 12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lara J LaCaille, PhD, University of Minnesota
  • Principal Investigator: Jennifer F Schultz, PhD, University of Minnesota

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2010

Primary Completion (Actual)

November 1, 2011

Study Completion (Actual)

December 1, 2011

Study Registration Dates

First Submitted

April 24, 2012

First Submitted That Met QC Criteria

April 24, 2012

First Posted (Estimated)

April 25, 2012

Study Record Updates

Last Update Posted (Actual)

December 22, 2023

Last Update Submitted That Met QC Criteria

December 21, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 1002S78225

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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