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Evaluation of the Effectiveness of a Comprehensive Visceral Adiposity-Focused Anti-Obesity Program

2

20Lighter

Status

Completed

Conditions

Hypertension
Visceral Obesity
Dyslipidemias
Obesity, Visceral
Central Obesity
Obesity
Type 2 Diabetes
Metabolic Disease
Obesity, Morbid

Treatments

Other: 20Lighter anti-obesity program

Study type

Observational

Funder types

Industry

Identifiers

NCT04807959
2016-443A

Details and patient eligibility

About

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.

Full description

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.

Enrollment

2,200 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • BMI >25
  • ability to stand on platform for body composition analysis

Exclusion criteria

  • Pregnant at time of enrollment
  • Breastfeeding at time of enrollment
  • Undergoing treatment for cancer at time of enrollment
  • History of major organ transplant with immunosuppressant medication
  • Over the 70 years of age with diagnosis of three cardiovascular comorbidities at time of enrollment
  • Adult with a vegetarian diet
  • Diagnosis of psychiatric conditions including: schizophrenia, bipolar disorder, manic depression

Trial design

2,200 participants in 1 patient group

20Lighter Program Participants
Description:
All enrolled subjects will have completed a 20Lighter anti-obesity program prior to enrollment.
Treatment:
Other: 20Lighter anti-obesity program

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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