Preliminary Data for Breath Biofeedback of Dietary Compliance

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2010 by University of Wisconsin, Madison.
Recruitment status was  Active, not recruiting
Information provided by:
University of Wisconsin, Madison Identifier:
First received: December 15, 2009
Last updated: January 6, 2010
Last verified: January 2010

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
Other: Dietary Adherence

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: 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 ] [ Designated as safety issue: No ]

Enrollment: 6
Study Start Date: July 2009
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: Dietary Adherence
    Subjects consumed a specified healthy, balanced, reduced calorie diet and provided timed breath samples.

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Healthy males or females age 18 or older

Exclusion Criteria:

  • Chronic disease
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01043783

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

No publications provided

Responsible Party: Leah Whigham, Ph.D., Associate Scientist, Board of Regents of the University of Wisconsin System Identifier: NCT01043783     History of Changes
Other Study ID Numbers: M-2009-1107
Study First Received: December 15, 2009
Last Updated: January 6, 2010
Health Authority: United States: Institutional Review Board

Keywords provided by University of Wisconsin, Madison:
Obesity processed this record on August 31, 2015