Back to resultsValidation and Evaluation of a Portable Body Scanner for Determination of Obesity
Primary Purpose
Obesity
Status
Completed
Phase
Locations
United States
Study Type
Observational
Intervention
Sponsored by
About this trial
This is an observational trial for Obesity focused on measuring Body Scanning, Body Fat, Body Volume, Obesity, No Conditions
Eligibility Criteria
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
Sites / Locations
- The Uniersity of Texas at Austin
Arms of the Study
Arm 1
Arm Type
Arm Label
1:one group
Arm Description
Outcomes
Primary Outcome Measures
Body volume
Secondary Outcome Measures
Validating body imaging as an indicator of central obesity
Full Information
NCT ID
NCT01049269
First Posted
January 13, 2010
Last Updated
June 23, 2015
Sponsor
University of Texas at Austin
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT01049269
Brief Title
Validation and Evaluation of a Portable Body Scanner for Determination of Obesity
Official Title
Validation and Evaluation of a Portable Body Scanner for Determination of Obesity
Study Type
Observational
2. Study Status
Record Verification Date
January 2007
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Texas at Austin
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The objective of this study is to validate a portable 3D human body measurement system which will improve approaches in obesity assessment.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Body Scanning, Body Fat, Body Volume, Obesity, No Conditions
7. Study Design
Enrollment
180 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1:one group
Primary Outcome Measure Information:
Title
Body volume
Time Frame
3 hours
Secondary Outcome Measure Information:
Title
Validating body imaging as an indicator of central obesity
Time Frame
3 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Study Population Description
Subject will be 18-60 years old, BMI 18.50 to 39.99 kg/m3, and free of known diseases, who are Hispanic and Not Hispanic or Latino Whites.
Sampling Method
Non-Probability Sample
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeanne H. Freeland-Graves, Ph.D.
Organizational Affiliation
The University of Texas at Austin
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Uniersity of Texas at Austin
City
Austin
State/Province
Texas
ZIP/Postal Code
78712
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Validation and Evaluation of a Portable Body Scanner for Determination of Obesity
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