- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02357329
Food Composition and Palatability (FCandP)
February 2, 2015 updated by: Richard Mattes, Purdue University
This study will investigate fat taste and if free fatty acids (FFA) in food function as a signal for fat content.
FFA are quite unpleasant - the investigators want to measure if the concentration in different foods correlates with hedonic preference.
FFA concentration from a variety of foods will be used to determine if people who have greater sensitivity for FFA find foods with higher FFA concentrations less acceptable.
Further, this study with determine whether the relationship between fat taste and hedonic food preference is modified by sex and body mass index (BMI).
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
52
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Indiana
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W. Lafayette, Indiana, United States, 47907
- Purdue Univeristy
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 64 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
unselected convenience sample
Description
Inclusion Criteria:
- Age 18-64
- Healthy
- Non-smoker
Exclusion Criteria:
- Food allergies
- Inability to detect and identify basic tastes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Taste and hedonic ratings of NEFA
Linoleic acid solutions from 0.005% to 1.58%.
Participants swish and spit 10 - 7.5mL solutions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
NEFA sensitivity (Participants will taste and rate 10 solutions based on intensity)
Time Frame: 1 day
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Participants will taste and rate 10 solutions based on intensity
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1 day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Food consumption and preference (Participants will answer questions regarding consumption of foods and preference)
Time Frame: 1 day
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Participants will answer questions regarding consumption of foods and preference.
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1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2014
Primary Completion (Actual)
November 1, 2014
Study Completion (Actual)
November 1, 2014
Study Registration Dates
First Submitted
December 22, 2014
First Submitted That Met QC Criteria
February 2, 2015
First Posted (Estimate)
February 6, 2015
Study Record Updates
Last Update Posted (Estimate)
February 6, 2015
Last Update Submitted That Met QC Criteria
February 2, 2015
Last Verified
December 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- 055-0390
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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