N/A
N=138
Evaluation of the Accuracy of a Computer Vision-based Tool for Assessment of Total Body Fat Percentage
Obesity
Bottom Line
View on ClinicalTrials.gov: NCT04854421 ↗Enrolled (actual)
138
Serious AEs
0.0%
Results posted
Aug 2024
Primary outcome: Primary: Comparison of Body Fat Percentage Estimates to DXA References Classified by Body Mass Index — 2.50; 6.36; 5.75; 7.66 Total Body Fat Percentage
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- VBC (Device)
- Age
- Adult, Older Adult · 21+ yrs
- Sex
- All
- Sponsor
- Pennington Biomedical Research Center
- Primary completion
- Dec 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Comparison of Body Fat Percentage Estimates to DXA References Classified by Body Mass Index |
2.50; 6.36; 5.75; 7.66; 4.29; 4.41 | — |
| PRIMARY Comparison of Body Fat Percentage Estimates to DXA References Classified by Sex |
1.88; 4.53; 6.23; 4.11; 3.37; 5.01 | — |
Summary
This research study is designed to validate the precision and accuracy of body measurement and composition results from a novel 2D imaging device that operates through a smart-phone application. Measurement references will be obtained through dual energy x-ray absorptiometry, air displacement plethysmography, bioelectrical impedance analysis, manual anthropometry, and previously validated 3D optical scanners.
Eligibility Criteria
Inclusion Criteria
- Being either male or female
- Being from 21 to 80 years of age
- Having a body weight of less than 440 pounds
- Being willing to comply with the study procedures
Exclusion Criteria
- Being pregnant or attempting to become pregnant
- Having medical implants such as a pacemaker or metal joint replacements
- Having undergone any previous body altering procedures such as breast augmentation or amputation
- Having a body weight greater than 440 pounds
Data sourced from ClinicalTrials.gov (NCT04854421). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.