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Comparing Devices That Measure Body Fat and Lean Mass in Adults

Compares body composition measurements from different devices in healthy adults, including people with overweight.

Plain-language title generated from the registry record
Registry title: Redefining Evaluation of Adiposity and Leanness: Broadening Objective Diagnostics for Obesity

Key facts

Where
Boston, Menlo Park, and Phoenix, United StatesSee the 3 sites

Where in United States

  • Exponent BostonBoston, United StatesTaking people
  • Exponent Menlo ParkMenlo Park, United StatesTaking people
  • Exponent PhoenixPhoenix, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Foundation for the National Institutes of Health
Trial code
NCT07776678
Record updated
26 October 2026
Original description
The purpose of this study is to evaluate body composition across a variety of medical, professional, and commercial devices, including: bioelectrical impedance analysis (BIA) devices, 3-dimensional optical imaging (3DO), manual anthropometry measurements, dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI), and blood tests. The secondary study purpose is to compare body composition measurements from BIA devices, 3DO, and manual anthropometry measurements within a 1-week period for a subset of the study population.Read full original descriptionShow less

Redefining Evaluation of Adiposity and Leanness: Broadening Objective Diagnostics for Obesity (REAL-BODY)

The purpose of this study is to evaluate body composition across a variety of medical, professional, and commercial devices, including: bioelectrical impedance analysis (BIA) devices, 3-dimensional optical imaging (3DO), manual anthropometry measurements, dual-energy X-ray absorptiometry (DXA), magnetic resonance imaging (MRI), and blood tests. The secondary study purpose is to compare body composition measurements from BIA devices, 3DO, and manual anthropometry measurements within a 1-week period for a subset of the study population.

The study plans to enroll 300 healthy (having no life-threatening conditions or diseases; male and female) participants, 18 years of age or older.

Inclusion: Being willing to provide written informed consent prior to participation Being willing to complete the study visits and comply with the study procedures; Being willing to travel to the various study locations for On-site, DXA, MRI, and Phlebotomy visits; Being willing to change into appropriate form-fitting clothing for 3DO assessments and/or appropriate gowns for DXA and MRI imaging; Must have a BMI within the range of 18.5 - 45 kg/m2; Being willing to refrain from all food, drink, and substances for 8 hours prior to the On-site visit(s) and phlebotomy visit; Being willing to refrain from all food, drink, and substances for 4 hours prior to the DXA and MRI scan visits; Being willing to refrain from any exercise or vigorous physical activity for 24 hours prior to all visits; Stable weight (no more than 5 kg change) for 3 months prior to screening; If recruited in the Phoenix, AZ area, participants must be willing to drive yourself to the Phoenix Office location for the On-site Visits 1 and 2 (if applicable) located at the Exponent Phoenix Office.

Exclusion: Having medical implants, such as a pacemaker or metal joint replacements, or other metal implants contraindicated for MRI; Cosmetic implants, such as breast implants; Prior amputation or major body-altering surgery that could invalidate body composition estimates; Having claustrophobia or a history of claustrophobia; Known HIV infection; Known hydration abnormality (e.g., significant edema, end-stage renal disease, end-stage liver disease); Severe illness or life-threatening conditions such as end-stage kidney, liver, lung disease, NYHA III-IV heart failure, or active malignancy; Being pregnant or attempting to become pregnant; Having a height greater than DXA scanning limit (77 inches); Having a body weight greater than indicated for the equipment (400 lbs); Known Lipodystrophy.

ClinicalTrials.gov NCT07776678