Repeated Exposure to Umami Taste on Taste Perception, Hedonics, and Satiety

January 24, 2022 updated by: Cornell University

Does Repeated Dietary Exposure to Umami Taste Affect Umami Perception, Hedonics, or Satiety? A Randomized Controlled Study

The purpose of this study is to determine how repeated dietary exposure to umami taste affects umami taste perception, hedonics, food preferences, and satiety. Healthy adult subjects will consume a low glutamate vegetable broth daily for one month, where the experimental group's broth is supplemented with the umami-rich stimuli of monosodium glutamate (MSG) and the control group's low glutamate broth is matched for sodium (NaCl).

The investigators hypothesize that repeated dietary exposure to umami taste will:

  1. diminish umami suprathreshold intensity perception and hinder the ability to discriminate varying MSG concentrations
  2. decrease liking of umami-rich foods and shift preferences upwards towards more intense umami stimuli
  3. decrease satiation and decrease the satiating effect of a test meal

Study Overview

Study Type

Interventional

Enrollment (Actual)

64

Phase

  • Not Applicable

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 60 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Have normal sense of taste and smell (self-report)
  • Likes soups or broths (self-report)
  • Able to report to study site daily (self-report)

Exclusion Criteria:

  • Restrained eater (score > 12 on restrained eating subscale from Three Factor Eating Questionnaire)
  • BMI < 18 or > 25 kg/m2 (self-report)
  • Vegan (self-report)
  • Hypertensive or on low-sodium diet (self-report)
  • Allergic or sensitive to MSG (self-report)

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

  • Primary Purpose: BASIC_SCIENCE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Increased exposure to MSG
Subjects consume vegetable broth daily containing MSG
Subjects eat normal diet and consume 8 ounces of vegetable broth with added MSG one time per day for 1 month
SHAM_COMPARATOR: No change in exposure to MSG
Subjects consume low glutamate vegetable broth daily, sodium-matched to the broth of the experimental group with NaCl
Subjects eat normal diet and consume 8 ounces of low glutamate vegetable broth without MSG (sodium-matched with NaCl) one time per day for 1 month

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in umami taste intensity perception
Time Frame: 1 month (at baseline and post intervention)
Subjects rate the umami intensity of aqueous solutions and foods on the general Labeled Magnitude Scale before and after a month-long dietary supplementation to determine how perception changes with repeated exposure to umami taste
1 month (at baseline and post intervention)
Change in umami taste discrimination
Time Frame: 1 month (at baseline and post intervention)
Subjects rank solutions of varying umami intensity before and after a month-long dietary supplementation to determine how perception changes with repeated exposure to umami taste
1 month (at baseline and post intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in umami liking and preference
Time Frame: 1 month (at baseline and post intervention)
Subjects rate liking and preference in a variety of umami-rich foods before and after a month-long dietary supplementation to determine how liking and preference of umami-rich foods changes with repeated exposure to umami taste
1 month (at baseline and post intervention)
Change in liking and wanting of high protein foods
Time Frame: 1 month (at baseline and post intervention)
Subjects complete the Leeds Food Preference Questionnaire before and after a month-long dietary supplementation to determine how explicit liking and implicit wanting of high-protein foods changes with repeated exposure to umami taste
1 month (at baseline and post intervention)
Change in satiation
Time Frame: 1 month (at baseline and post intervention)
Subjects consume a test meal and the amount of food eaten is measured before and after a month-long dietary supplementation to determine how satiation from a test meal differs after repeated exposure to umami taste
1 month (at baseline and post intervention)
Change in satiety
Time Frame: 1 month (at baseline and post intervention)
Subjects consume a test meal and rate appetite sensations on a visual analog scale throughout the test meal before and after a month-long dietary supplementation. A satiety quotient will be derived from these values with the formula: Satiety Quotient = (rating pre-eating episode-rating post-eating episode) / (intake of eating episode) to determine how satiety changes with repeated exposure to umami taste
1 month (at baseline and post intervention)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Height
Time Frame: 1 month (at baseline and post intervention)
Body height (centimeters) will be measured with standard procedures and equipment. Using this information, BMI will be calculated with the formula: BMI=[kg/m]2 to ensure that BMI does not change with repeated exposure to umami taste
1 month (at baseline and post intervention)
Weight
Time Frame: 1 month (at baseline and post intervention)
Body weight (kilograms) will be measured with standard procedures and equipment. Using this information, BMI will be calculated with the formula: BMI=[kg/m]2 to ensure that BMI does not change with repeated exposure to umami taste
1 month (at baseline and post intervention)
Habitual glutamate consumption
Time Frame: 1 month (at baseline and post intervention)
Subjects complete the National Cancer Institute's monthly diet history questionnaire to estimate habitual glutamate consumption. Baseline habitual glutamate consumption, in addition to gender, will be assessed as effect modifiers in the analysis.
1 month (at baseline and post intervention)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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, 2016

Primary Completion (ACTUAL)

November 1, 2016

Study Completion (ACTUAL)

November 1, 2016

Study Registration Dates

First Submitted

December 15, 2016

First Submitted That Met QC Criteria

January 3, 2017

First Posted (ESTIMATE)

January 5, 2017

Study Record Updates

Last Update Posted (ACTUAL)

February 7, 2022

Last Update Submitted That Met QC Criteria

January 24, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 1608006563

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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