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OpenTrials
Completed

NCT Number: NCT01049269

Validation and Evaluation of a Portable Body Scanner for Determination of Obesity

The objective of this study is to validate a portable 3D human body measurement system which will improve approaches in obesity assessment.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The Uniersity of Texas at Austin

Austin, Texas, 78712, United States

About this study

Obesity has become an epidemic in the United States. A new technique of three-dimensional (3 D) photonic scanning will be used to create and validate a portable instrument that rapidly assesses obesity in clinical and field settings. This new portable body scanner will be a safe and easy method to help determine the incidence and type of obesity.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-60 years old
  • BMI between 18.50 to 39.99 kg/m3
  • Free of known diseases
  • Hispanic and Not Hispanic or Latino Whites

Exclusion criteria

  • Women who are pregnant, could be pregnant, or lactating

Treatment and study plan

Primary outcomes

  1. Body volume

    Time frame: 3 hours

Secondary outcomes

  1. Validating body imaging as an indicator of central obesity

    Time frame: 3 hours

Sponsors and collaborators

Lead sponsor

University of Texas at Austin

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Important dates

Study start
2007
Primary completion
2013
Study completion
2013
First posted
Jan 14, 2010
Registry last updated
Jun 25, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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