NCT01049269

Completed

Validation and Evaluation of a Portable Body Scanner for Det...

University of Texas at Austin Source

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Other study identifiers

Sponsor study identifier

R01DK081206

Secondary identifiers

5R21DK081206

NIH

Study Type

observational

Actual enrollment (reported)

180

Locations

1 country

Sites

1

Timeline

Study Start

January 2007

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

July 2013

Actual (reported)

Study Completion

July 2013

Actual (reported)

Brief Summary

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

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 180 participants
Study completion date: July 2013
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 2007
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
January 13, 2010
Actual (reported)
First Posted
January 14, 2010
Actual (reported)
Primary Completion
July 2013
Actual (reported)
Study Completion
July 2013
Actual (reported)

Last Updated: June 25, 2015
Status Verified: January 2007
Last Update Submitted: June 23, 2015

Conditions

Obesity

Keywords

Body ScanningBody FatBody VolumeObesityNo Conditions

Outcome Measures

Primary Outcomes (1)

Body volume
3 hours

Secondary Outcomes (1)

Validating body imaging as an indicator of central obesity
3 hours

Study Arms (1)

1:one group

Eligibility Criteria

Age18 Years - 60 Years

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64)

Sampling MethodNon-Probability Sample

Study Population

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.

You may qualify if:

years old

Sponsors & Collaborators

University of Texas at Austin
Otherlead
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIHcollaborator

Study Sites (1)

The Uniersity of Texas at Austin

Austin, Texas, 78712, United States

MeSH Terms

Conditions

Obesity

Condition Hierarchy (Ancestors)

OverweightOvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

Jeanne H. Freeland-Graves, Ph.D.
The University of Texas at Austin
PRINCIPAL INVESTIGATOR

Enrollment

180 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

January 13, 2010

First Posted

January 14, 2010

Study Start

January 2007

Date type not reported

This date has not been verified as actual or estimated.

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BMI between 18.50 to 39.99 kg/m3

Free of known diseases

Hispanic and Not Hispanic or Latino Whites

You may not qualify if:

Women who are pregnant, could be pregnant, or lactating

Contact the study team to confirm eligibility.

Primary Completion

July 2013

Actual (reported)

Study Completion

July 2013

Actual (reported)

Last Updated

June 25, 2015

Record last verified: 2007-01

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT01049269
Data provider: ClinicalTrials.gov
Source updated: 2015-06-25
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:20:07 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

1:one group

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations