- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03010930
Repeated Exposure to Umami Taste on Taste Perception, Hedonics, and Satiety
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:
- diminish umami suprathreshold intensity perception and hinder the ability to discriminate varying MSG concentrations
- decrease liking of umami-rich foods and shift preferences upwards towards more intense umami stimuli
- decrease satiation and decrease the satiating effect of a test meal
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
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