St. Luke's Hospital and Clinics
Duluth, Minnesota, 55805, United States
NCT Number: NCT01585480
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).
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Duluth, Minnesota, 55805, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
a. Identification and training of influential employees (Peer Helpers) to shape healthy norms
Time frame: Baseline, 6 months, 12 months
Time frame: Baseline, 6 months,12 months
Time frame: Baseline, 6 months, 12 months
Eating behaviors will be assessed by the Multifactor Screener (self-report questionnaire) and food purchase data (objective).
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.
University of Minnesota
Other
Acronym: Go!
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06127251
Behavior, Body Weight
Atlanta, Georgia, United States
View Trial DetailsNCT01809288
Behavior, Body Weight
Bethesda, Maryland, United States
View Trial DetailsNCT00063674
Adherence Interventions, Behavior
Palo Alto, California, United States
View Trial DetailsNCT06471569
Behavior, Body Weight
Durham, North Carolina, United States
View Trial Details