AzTrials
AzTrials

Umami Taste PerceptionNCT03010930

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

A study testing Supplementation of diet with MSG and No supplementation of diet with MSG in people with Umami Taste Perception, run by Cornell University.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

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… Read more about this study

Who is it for?
Ages 18 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Umami Taste Perception
What is being tested?
Supplementation of diet with MSG and No supplementation of diet with MSG
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
64 participants
Where
No sites listed yet
Study dates
Oct 2016to Nov 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

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

Who cannot join

  • 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)

About this study

Official title: 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
Being tested
Supplementation of diet with MSG, No supplementation of diet with MSG

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Supplementation of diet with MSGOther

    Subjects eat normal diet and consume 8 ounces of vegetable broth with added MSG one time per day for 1 month

  • No supplementation of diet with MSGOther

    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

Study groups in NCT03010930
Study groupRoleWhat they receive
Increased exposure to MSGExperimentalSubjects consume vegetable broth daily containing MSG
Receives: Other: Supplementation of diet with MSG
No change in exposure to MSGSham comparatorSubjects consume low glutamate vegetable broth daily, sodium-matched to the broth of the experimental group with NaCl
Receives: Other: No supplementation of diet with MSG

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in umami taste intensity perception

    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

    Measured: 1 month (at baseline and post intervention)

  2. Change in umami taste discrimination

    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

    Measured: 1 month (at baseline and post intervention)

Secondary outcomes (4)
  1. Change in umami liking and preference

    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

    Measured: 1 month (at baseline and post intervention)

  2. Change in liking and wanting of high protein foods

    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

    Measured: 1 month (at baseline and post intervention)

  3. Change in satiation

    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

    Measured: 1 month (at baseline and post intervention)

  4. Change in satiety

    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

    Measured: 1 month (at baseline and post intervention)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Jan 2017 (estimated)
  2. Study startOct 2016
  3. Primary completionNov 2016
  4. Study completionNov 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
64 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03010930
Sponsor's protocol ID
1608006563
Status last verified
Jan 2022
First submitted
15 Dec 2016
Last updated
7 Feb 2022
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Noel CA, Finlayson G, Dando R. Prolonged Exposure to Monosodium Glutamate in Healthy Young Adults Decreases Perceived Umami Taste and Diminishes Appetite for Savory Foods. J Nutr. 2018 Jun 1;148(6):980-988. doi: 10.1093/jn/nxy055.

    PubMed 29796671

Questions about this trial

What is this clinical trial studying?

A study testing Supplementation of diet with MSG and No supplementation of diet with MSG in people with Umami Taste Perception, run by Cornell University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 7 Feb 2022. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in umami taste intensity perception (time frame: 1 month (at baseline and post intervention)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03010930, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Feb 2022.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in