MedPath

Smart Technology for Weight Loss and Metabolic Health

Not Applicable
Completed
Conditions
Obesity
Weight Loss
Overweight
Prediabetes
Lifestyle
Interventions
Behavioral: Standard Weight Management Visits
Device: Wearable technology, smartscale
Behavioral: Smartphone applications
Registration Number
NCT02742662
Lead Sponsor
Temple University
Brief Summary

The study will evaluate whether a technology-based lifestyle intervention program using primarily a smartphone platform is an acceptable and effective way for treating obesity. The goal of the program is to achieve weight loss and enhance the health of overweight or obese subjects by improving their diet and activity via smartphone applications as compared with conventional in-person weight management programs.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
29
Inclusion Criteria
  • Overweight or obese BMI 25-42 kg/m2
  • Employed in sedentary occupations
  • Own a personal smartphone with unlimited data plan or >4 GigaByte data
  • Proficient with use of smartphone applications and technology with current daily usage
  • Ability to engage in moderate intensity exercise
  • Weight stability for the last 2 months
  • Participants must be willing to comply with all study-related procedures
Exclusion Criteria
  • Current or planned pregnancy
  • Cardiovascular, pulmonary, renal disease, joint disease
  • Uncontrolled thyroid disease
  • History of eating disorders, psychiatric disease
  • History of substance abuse or dependence in the last 1 year
  • Diabetes
  • Shift work
  • Previous weight loss surgery
  • Use of weight loss drugs/diet/program in the last 6 weeks
  • Inability to increase walking as a form of exercise and to engage in moderate intensity exercise
  • Other conditions or medications that affect body weight/appetite/metabolism
  • Serious or unstable medical or psychological conditions that would compromise the subject's safety for successful participation
  • Incapable of adhering with an intensive lifestyle intervention using technology and smartphone applications

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Smart Technology GroupSmartphone applicationsThe Smart Technology Group will receive a technology-based lifestyle intervention program which uses wearable technology, smartscales and smartphone applications to track and deliver feedback on caloric expenditure, physical activity, caloric intake and body weight. Participants will receive information through smartphone applications on strategies to make changes to their diet, physical activity, and weight-related behaviors along with standard 3 monthly in-person weight management visits.
Standard Weight Management GroupStandard Weight Management VisitsThe Standard Weight Management Group will receive 3 monthly in-person weight management visits during which they will receive standard of care lifestyle recommendations in accordance with the 2013 American Heart Association/American College of Cardiology/The Obesity Society Guideline.
Smart Technology GroupWearable technology, smartscaleThe Smart Technology Group will receive a technology-based lifestyle intervention program which uses wearable technology, smartscales and smartphone applications to track and deliver feedback on caloric expenditure, physical activity, caloric intake and body weight. Participants will receive information through smartphone applications on strategies to make changes to their diet, physical activity, and weight-related behaviors along with standard 3 monthly in-person weight management visits.
Smart Technology GroupStandard Weight Management VisitsThe Smart Technology Group will receive a technology-based lifestyle intervention program which uses wearable technology, smartscales and smartphone applications to track and deliver feedback on caloric expenditure, physical activity, caloric intake and body weight. Participants will receive information through smartphone applications on strategies to make changes to their diet, physical activity, and weight-related behaviors along with standard 3 monthly in-person weight management visits.
Primary Outcome Measures
NameTimeMethod
Change in body weight in kg6 months
Secondary Outcome Measures
NameTimeMethod
Change from baseline blood pressure12 months
Change from baseline waist circumference12 months
Change from baseline insulin resistance by homeostasis model assessment (HOMA-IR)6 months
Change from baseline hemoglobin A1c6 months
Change from baseline plasma triglycerides6 months
Change from baseline body weight in kg12 months
Change in Quality of Life6 months after receiving the intervention

SF36 Questionnaire in wait-listed control group after the intervention

Change in insulin resistance by homeostasis model assessment (HOMA-IR)12 months compared to baseline and 6 months after receiving the intervention

Wait-listed control group

Change in hemoglobin A1c12 months compared to baseline and 6 months after receiving the intervention and from baseline

Wait-listed control group

Change in plasma triglycerides12 months compared to baseline and 6 months after receiving the intervention

Wait-listed control group

Trial Locations

Locations (1)

Temple University

🇺🇸

Philadelphia, Pennsylvania, United States

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