A retrospective review of body composition outcomes of participants of a comprehensive visceral-fat focused anti-obesity program. Data from approximately 2000-2500 participants are expected to be included in the study.
This is a retrospective, multi-center clinical study to evaluate the efficacy of the 20Lighter comprehensive anti-obesity program in reducing body composition measures including body weight, body fat, visceral adiposity, intracellular fluid, and other metrics of interest. Anecdotal evidence on reductions of prescription medication, chronic health issues, and improvements in quality of life will be gauged via review of patient assessment forms and surveys.
Study Type
OBSERVATIONAL
Enrollment
2,200
A customized expert supervised 3-phase program including non-invasive proprietary nutritional, behavioral, and physiological components.
Reduction of Visceral Adiposity
% reduction of visceral adiposity (as measured by visceral fat rating) measured via an FDA-cleared Class 2 medical device with Bioelectrical Impedance Analysis (BIA) via bipolar foot electrodes.
Time frame: Change from baseline to program completion (60 Days)
Reduction of Body Weight
% reduction of body weight measured via an FDA-cleared Class 2 medical device with Bioelectrical Impedance Analysis (BIA) via bipolar foot electrodes.
Time frame: Change from baseline to program completion (60 Days)
Reduction of Body Mass Index
% reduction of body mass index measured via an FDA-cleared Class 2 medical device with Bioelectrical Impedance Analysis (BIA) via bipolar foot electrodes.
Time frame: Change from baseline to program completion (60 Days)
Reduction of Body Fat
% reduction of body fat measured via an FDA-cleared Class 2 medical device with Bioelectrical Impedance Analysis (BIA) via bipolar foot electrodes.
Time frame: Change from baseline to program completion (60 Days)
Increase of Intracellular Fluid
% increase of intracellular fluid (as measured by body water %) measured via an FDA-cleared Class 2 medical device with Bioelectrical Impedance Analysis (BIA) via bipolar foot electrodes.
Time frame: Change from baseline to program completion (60 Days)
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