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Preliminary Data for Breath Biofeedback of Dietary Compliance

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01043783
First Posted: January 7, 2010
Last Update Posted: October 8, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University of Wisconsin, Madison
  Purpose
The investigators ultimate goal is to test the hypothesis that immediate feedback of dietary adherence will enhance compliance to a weight loss program. This study deals directly with gathering the needed preliminary data for a grant submission.

Condition Intervention
Obesity Other: Dietary Adherence

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Preliminary Data for Breath Biofeedback of Dietary Compliance

Further study details as provided by University of Wisconsin, Madison:

Primary Outcome Measures:
  • Breath CO2, ketones, aldehydes, alcohols [ Time Frame: Daily for 5-7 days ]

Enrollment: 6
Study Start Date: July 2009
Study Completion Date: April 2011
Intervention Details:
    Other: Dietary Adherence
    Subjects consumed a specified healthy, balanced, reduced calorie diet and provided timed breath samples.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy males or females age 18 or older

Exclusion Criteria:

  • Chronic disease
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01043783


Locations
United States, Wisconsin
University of Wisconsin-Madison
Madison, Wisconsin, United States, 53792
Sponsors and Collaborators
University of Wisconsin, Madison
  More Information

Responsible Party: University of Wisconsin, Madison
ClinicalTrials.gov Identifier: NCT01043783     History of Changes
Other Study ID Numbers: M-2009-1107
First Submitted: December 15, 2009
First Posted: January 7, 2010
Last Update Posted: October 8, 2015
Last Verified: October 2015

Keywords provided by University of Wisconsin, Madison:
Obesity