- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01585480
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
Intervention / Treatment
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
|
|
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.
Sponsor
Collaborators
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
Additional Relevant MeSH Terms
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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