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Healthy Futures Project: A Community Based Obesity Prevention Program

SWITCH: Rationale, Design, and Implementation of a Community, School, and Family-based Intervention to Modify Behaviors Related to Childhood Obesity

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00685555
Acronym
SWITCH
Enrollment
1300
Registered
2008-05-28
Start date
2005-10-31
Completion date
2006-12-31
Last updated
2011-06-23

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

Conditions

Obesity, Overweight

Keywords

Screen time, Fruits and Vegetable Consumption, Physical Activity, Obesity, Overweight

Brief summary

The purpose of this research is to increase community awareness about the relationship between physical activity, screen time, and nutrition and how these factors influence healthy weight management. The problem of obesity is at epidemic proportions and has become the most important public health problem confronting the United States today. Of greatest concern is the 300% increase in obesity rates among children and youth over the past twenty years. Childhood obesity is a precursor of adult obesity.

Detailed description

The Switch™ Program is a unique community and family-based behavior change initiative that helps motivate children to change three critical health behaviors that are risk factors for childhood overweight and obesity. Through community education, family-based strategies and partnerships with schools, 3rd, 4th and 5th graders are encouraged to: Switch what you Do™ Switch what you View™ Switch what you Chew™.

Interventions

BEHAVIORALSwitch active lifestyles brought to you by MediaWise

The Switch™ Program is a unique community and family-based behavior change initiative that helps motivate children to change three critical health behaviors that are risk factors for childhood overweight and obesity.

BEHAVIORALSwitch active lifestyles from MediaWise

1300 students (male and female) were recruited through two separate school districts in Lakeville, Minnesota and Cedar Rapids, Iowa. Informed consents went to all students who chose to participate. Demonstration and Control school were randomly selected. Baseline data was collected regarding physical activity, screen time, and nutrition, standard body measurements, and baseline data, and salivary cortisol levels were taken. Parent and teacher surveys were also conducted. After baseline selected demonstration sites and students were provided with information focused on improving healthy behaviors while the control sites served as matched comparison groups.

Sponsors

Fairview Health Services
CollaboratorOTHER
Medica
CollaboratorUNKNOWN
Healthy and Active America Foundation,
CollaboratorUNKNOWN
Cargill
CollaboratorINDUSTRY
Spunk Design Machine
CollaboratorUNKNOWN
Iowa State University
CollaboratorOTHER
Michigan State University
CollaboratorOTHER
University of Minnesota
CollaboratorOTHER
National Institute on Media and the Family
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 13 Years
Healthy volunteers
Yes

Inclusion criteria

* All children in 3-5 grades who provide parental consent and child assent will be eligible to participate in the project.

Exclusion criteria

* Participants who meet the following

Design outcomes

Primary

MeasureTime frame
Our outcome measure was reduction of screen time4 waves of data

Secondary

MeasureTime frame
Our secondary outcome measure increase in fruit and vegetable consumption.T1-PRE Intervention toT2 Post Intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 5, 2026