Reducing Sedentary Time in Obese Adults
Study Details
Study Description
Brief Summary
Greater time spent in sedentary behaviors, independent of physical activity level, can increase risk of morbidity and mortality. Objective assessments indicate that bariatric surgery patients spend large amounts of time in sedentary behaviors. The present study is the first to test whether a mobile health (mHealth) approach that employs widely adopted smartphone technology to monitor and modify sedentary behaviors as they occur is a feasible and acceptable method of reducing sedentary time in these patients and other obese populations.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Behavioral intervention Behavioral intervention to reduce sedentary time delivered via mobile smartphone |
Behavioral: Behavioral intervention to reduce sedentary time delivered via mobile smartphone
The overall goals of the intervention are to decrease overall sedentary time and to increase the number of breaks in sedentary time. The intervention approach combines an advanced smartphone device with an on-board accelerometer and a sophisticated smartphone application to: 1) monitor participants sedentary behavior in real time in their natural environment; and 2) use monitored data to deliver immediate, individually-tailored, goal-driven prompts and feedback to encourage substitute of sedentary behaviors with physical activity.
|
Outcome Measures
Primary Outcome Measures
- Average daily sedentary minutes [4 weeks]
Secondary Outcome Measures
- Average daily adherence to prompts to reduce sedentary time delivered via mobile smartphone [4 weeks]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Bariatric surgery patients and other obese individuals will be considered
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Body mass index >= 30 kg/m2
Exclusion Criteria:
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Report being unable to engage in daily activities and walk continuously for >= 10 minutes without assistance
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Are currently involved in a physical activity intervention.
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Are unable to read or understand the study materials
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Are currently taking medications that cause dizziness and/or feeling faint when sitting or standing.
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Report any condition that in the opinion of investigators would preclude adherence to the intervention protocol including plans to relocate, history of substance abuse or other significant psychiatric problems, or terminal illness.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Weight Control and Diabetes Research Center | Providence | Rhode Island | United States | 02903 |
Sponsors and Collaborators
- The Miriam Hospital
- National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Investigators
- Principal Investigator: Dale S Bond, Ph.D., The Miriam Hospital/Brown Alpert Medical School
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 1R03DK095740-01