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Clinical Trials/NCT02160834
NCT02160834
Withdrawn
Not Applicable

A Mobile Health Approach to Reducing Sedentary Time in Bariatric Surgery Patients

The Miriam Hospital1 site in 1 countryJanuary 2014
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
The Miriam Hospital
Locations
1
Primary Endpoint
Change in percentage of daily sedentary time from baseline to post-intervention.
Status
Withdrawn
Last Updated
11 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
December 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Bariatric surgery patients and other obese individuals will be considered
  • Body mass index \>= 25 kg/m2

Exclusion Criteria

  • Report being unable to engage in daily activities and walk continuously for \>= 10 minutes without assistance
  • Are currently involved in a physical activity intervention.
  • Are unable to read or understand the study materials
  • Are currently taking medications that cause dizziness and/or feeling faint when sitting or standing.
  • 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.

Outcomes

Primary Outcomes

Change in percentage of daily sedentary time from baseline to post-intervention.

Time Frame: 8 weeks

Secondary Outcomes

  • Change in percentage of daily sedentary time from baseline to follow-up(12 weeks)

Study Sites (1)

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