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CompletedNCT02357329FCandPUpdated Feb 6, 2015

Food Composition and Palatability

An observational study in Fat Taste, sponsored by Purdue University. Completed at 1 site in United States. Open to participants aged 18 Years to 64 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-02-06.

Sponsored by Purdue University · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
52
Ages
18 Years to 64 Years
Sex
All
01

Study summary

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).

02

Conditions studied

  • Fat Taste

Keywords

  • fat taste
  • food preference
  • consumption
  • free fatty acids
03

In context

Lead sponsor

Purdue University is the lead sponsor of 168 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 64 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

unselected convenience sample

Inclusion criteria

  • Age 18-64
  • Healthy
  • Non-smoker

Exclusion criteria

Exclusion Criteria:

  • Food allergies
  • Inability to detect and identify basic tastes
05

Study design

Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
52 participants (actual)
Patient registry
No

Groups and cohorts

  • Taste and hedonic ratings of NEFA

    Linoleic acid solutions from 0.005% to 1.58%. Participants swish and spit 10 - 7.5mL solutions.

06

What researchers measure

Primary outcomes

  1. NEFA sensitivity (Participants will taste and rate 10 solutions based on intensity)

    Participants will taste and rate 10 solutions based on intensity

    Time frame: 1 day

Secondary outcomes

  1. Food consumption and preference (Participants will answer questions regarding consumption of foods and preference)

    Participants will answer questions regarding consumption of foods and preference.

    Time frame: 1 day

07

Study locations

1 site
  • Purdue Univeristy
    W. Lafayette, Indiana 47907, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 6, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02357329
Lead sponsor
Purdue University
Responsible party
Richard Mattes (Distinguished Prof. Nutrition Sciences, Purdue University) — Principal investigator
First posted
Feb 6, 2015
Start date
Oct 2014
Primary completion
Nov 2014
Completion
Nov 2014
Last update
Feb 6, 2015
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2014. You cannot join it, but the record below documents what was studied.

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