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CompletedNCT07421466OptUmamiUpdated Feb 19, 2026

Umami Taste Intensity and Meal Intake

An interventional study of Hedonic mapping and Ad libitum risotto test meal in Taste Sensitivity, Umami Taste Perception and Food Intake Regulation, sponsored by Wageningen University. Completed at 1 site in Netherlands. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-19.

Sponsored by Wageningen University · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
47
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

Sweet and salty tastes can influence food intake. Increased intensity of these tastes has been shown to decrease food intake and increase satiation compared to the less intense taste, independent of palatability. Umami taste intensity has been shown to reduce subsequent food intake, especially when paired with protein content in foods. Taste can be related with nutrient content of the diet, with sweet foods having carbohydrates, salty foods containing sodium, and umami foods containing protein.

However, no study has yet investigated the impact of umami and food intake, using the approach of similar palatability and differing taste intensity levels. Given its relationship with nutrient signaling, it is important to explore the relationship between umami intensity and satiation. Therefore, this study aims to compare ad libitum food intake of two levels with similar palatability and differing umami taste intensities (high and low) to food intake from a meal with optimum taste intensity.

Study population 40-50 healthy, normal weight participants from Wageningen and surroundings will be included. Previous studies have applied this method in sweet and salty tastes with 15-59 participants.

Test session 1: Hedonic mapping Determine individual's most preferred level of umami taste in 6 risotto samples, using pairwise staircase comparison. Samples will contain a fixed level of salt (0.2 w/w%), and MSG concentrations ranging from 0.2-2.1 w/w%. Per individual, The optimal tasting MSG intensity will be selected based on forced choice.

Test session 2, 3 and 4: ad libitum risotto lunch meals In a randomized cross-over design, participants will receive the optimum, high and low MSG risotto. The following will be measured:

  • Test meal consumption (primary outcome);
  • Meal liking after one bite;
  • Water consumption;
  • Absolute taste intensity ratings of the meal;
  • Relative taste intensity ratings of the meal;
  • Habitual dietary taste exposure (tasteFFQ).

Study procedures Subjects will be provided with a standardized breakfast and to not consume anything between breakfast and lunch session. This will be validated upon arrival to the lunch meal. They will also be asked to refrain from eating for one hour after the test session. Participants will be asked to fill in the tasteFFQ, to investigate the link between dietary taste patterns and hedonic umami taste ratings.

Data analysis Data will be analyzed using Rstudio. First, normality will be assessed, and data will be normalized if needed. Difference in food intake in grams between the three intensities will be compared using ANOVA. A post-hoc test will be applied if statistical outcomes are significant. Categorical variables will be compared using Chi-square test.

02

Conditions studied

  • Taste Sensitivity
  • Umami Taste Perception
  • Food Intake Regulation
  • Hedonic Function
  • Palatability

Keywords

  • umami
  • savoury
  • ad libitum
  • taste intensity
  • palatability
  • food intake
  • hedonic mapping
  • PCA
  • MSG
03

In context

Lead sponsor

Wageningen University is the lead sponsor of 150 studies on the registry; 15 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Self-reported healthy;
  • BMI between 18.5 and 25 kg/m2;
  • Age between 18 and 55 years old;
  • Able to visit the research facilities on the Wageningen campus for hedonic mapping (once) and for the risotto lunch meal (three times);
  • Able to provide informed consent.

Exclusion criteria

Exclusion Criteria:

  • Diagnosed with smell- or taste disorder(s);
  • Use of medication that could influence taste ability and/or food intake behaviour;
  • Food allergy or intolerance to any of the ingredients used in the ad libitum test meal;
  • Consumption of more than 14 (women) or 21 (men) glasses of alcohol per week;
  • Student or personnel of the Health Research Unit at Wageningen University
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
47 participants (actual)

Study arms

  • Experimental
    Low umami taste intensity

    The low umami intensity meal will have a taste intensity corresponding with a lower than ideal than the MSG concentration in the sample that came out as 'winner' by forced choice during the first test session in which umami taste preferences per individual will be assessed by hedonic mapping (PCA). The palatability ratings of the lower than ideal will correspond to the palatability ratings of the higher than ideal condition.

    Other: Hedonic mapping · Other: Ad libitum risotto test meal

  • Experimental
    Ideal umami taste intensity

    The ideal umami intensity meal will have a taste intensity corresponding with the MSG concentration in the sample that came out as 'winner' by forced choice during the first test session in which umami taste preferences per individual will be assessed by hedonic mapping (PCA).

    Other: Hedonic mapping · Other: Ad libitum risotto test meal

  • Experimental
    high umami taste intensity

    The high umami intensity meal will have a taste intensity corresponding with a higher than ideal than the MSG concentration in the sample that came out as 'winner' by forced choice during the first test session in which umami taste preferences per individual will be assessed by hedonic mapping (PCA). The palatability ratings of the higher than ideal will correspond to the palatability ratings of the lower than ideal condition.

    Other: Hedonic mapping · Other: Ad libitum risotto test meal

Interventions

  • OtherHedonic mapping

    During the first session, participants will be presented with 2 risotto samples simultaneously, differing in MSG content and thus umami taste intensity, by PCA. First, samples will be presented in ascending concentration, with the best rated sample (forced choice) from the previous round, and the next concentration. This will be replicated in descending order. Based on these individual outcomes, umami taste intensities of the ad libitum test meals will be calculated per participant.

  • OtherAd libitum risotto test meal

    During the ad libitum test meal, participants will be presented with 1200 grams of risotto with either high-, low-, or optimum umami taste intensity.

06

What researchers measure

Primary outcomes

  1. Difference in food intake from ad libitum test meal between taste intensity conditions

    Difference in food intake in volume (grams) from the ad libitum test meal between the three (high-, low- and ideal) umami taste intensities.

    Time frame: Test session 2, 3 and 4 (week 2, 3 and 4)

Secondary outcomes

  1. Difference in test meal liking between taste intensity conditions

    Difference in test meal liking (VAS) between the three (high-, low- and ideal) umami taste intensities.

    Time frame: Test session 2, 3 and 4 (week 2, 3 and 4)

  2. Absolute difference in umami taste intensity ratings of the ad libitum test meal between taste intensity conditions

    Difference in absolute taste intensity ratings of the ad libitum test meal between the three (high-, low- and ideal) umami taste intensities. This will be rated after each lunch meal on a visual analogue scale (VAS).

    Time frame: Test session 2, 3 and 4 (week 2, 3 and 4)

  3. Relative difference in umami taste intensity ratings of the ad libitum test meal between taste intensity conditions

    Relative taste intensity ratings based on ranking. Participants will be asked to rank the three meals based on umami taste intensity after the 3rd lunch meal. Ranking will be used, with anchors "least intense" to "most intense".

    Time frame: Test session 4 (week 4)

  4. Difference in water consumption during the ad libitum test meal between taste intensity conditions

    Difference in water consumption in volume (grams) from the ad libitum test meal between the three (high-, low- and ideal) umami taste intensities

    Time frame: Test session 2, 3 and 4 (week 2, 3 and 4)

  5. Difference in reported appetite and fullness ratings between the three conditions

    Before and after the ad libitum test meals, appetite and fullness ratings of participants will be assessed on a Visual Analogue Scale (VAS). Differences of these rating between umami taste intensity conditions (low-, high- and ideal umami taste intensity) will be assessed. VAS 0-100 will be used, with anchors "Not at all" to "Extremely".

    Time frame: Test session 2, 3 and 4 (week 2, 3 and 4)

  6. Difference in test meal liking between taste intensity conditions

    Difference in test meal liking (VAS) between the three (high-, low- and ideal) umami taste intensities. VAS 0-100 will be used, with anchors "Not tasty at all" to "Extremely tasty".

    Time frame: Test session 2, 3 and 4 (week 2, 3 and 4)

  7. Habitual taste exposure

    Habitual taste exposure will be measured with a food frequency questionnaire (tasteFFQ) specifically designed to assess relative food intake based on taste cluster. Individual optimum umami intensity will be compared to habitual dietary taste exposure to the salt, umami and fat taste cluster, as well as to the intake of umami tasting food items. Participants will fill in the tasteFFQ directly after the first (hedonic mapping session) visit. The tasteFFQ inquires average daily food intake, measured with a reference period of the previous four weeks.

    Time frame: Participants will fill in the TasteFFQ directly after the first visit (hedonic mapping). The TasteFFQ captures average daily food intake over the previous four weeks (so food intake prior to study enrollment).

07

Study locations

1 site
  • Department of Human Nutrition, Wageningen University
    Wageningen, Gelderland, Netherlands
08

References and documents

Publications

  • Masic U, Yeomans MR. Umami flavor enhances appetite but also increases satiety. Am J Clin Nutr. 2014 Aug;100(2):532-8. doi: 10.3945/ajcn.113.080929. Epub 2014 Jun 18. PubMed 24944058 ↗
  • Sorensen LB, Moller P, Flint A, Martens M, Raben A. Effect of sensory perception of foods on appetite and food intake: a review of studies on humans. Int J Obes Relat Metab Disord. 2003 Oct;27(10):1152-66. doi: 10.1038/sj.ijo.0802391. PubMed 14513063 ↗
  • Bolhuis DP, Lakemond CM, de Wijk RA, Luning PA, de Graaf C. Effect of salt intensity on ad libitum intake of tomato soup similar in palatability and on salt preference after consumption. Chem Senses. 2010 Nov;35(9):789-99. doi: 10.1093/chemse/bjq077. Epub 2010 Aug 12. PubMed 20705808 ↗
  • Bolhuis DP, Lakemond CM, de Wijk RA, Luning PA, Graaf Cd. Both longer oral sensory exposure to and higher intensity of saltiness decrease ad libitum food intake in healthy normal-weight men. J Nutr. 2011 Dec;141(12):2242-8. doi: 10.3945/jn.111.143867. Epub 2011 Nov 2. PubMed 22049294 ↗
  • Bolhuis DP, Lakemond CM, de Wijk RA, Luning PA, de Graaf C. Effect of salt intensity in soup on ad libitum intake and on subsequent food choice. Appetite. 2012 Feb;58(1):48-55. doi: 10.1016/j.appet.2011.09.001. Epub 2011 Sep 29. PubMed 21986190 ↗
  • Masic U, Yeomans MR. Monosodium glutamate delivered in a protein-rich soup improves subsequent energy compensation. J Nutr Sci. 2014 Aug 13;3:e15. doi: 10.1017/jns.2014.15. eCollection 2014. PubMed 25191607 ↗
  • Forde, C. G. (2016). Flavor perception and satiation. In Flavor (pp. 251-276). Woodhead Publishing
  • Jayasena DD, Kang T, Wijayasekara KN, Jo C. Innovative Application of Cold Plasma Technology in Meat and Its Products. Food Sci Anim Resour. 2023 Nov;43(6):1087-1110. doi: 10.5851/kosfa.2023.e31. Epub 2023 Nov 1. PubMed 37969327 ↗

Individual participant data

Plan to share: Yes — Individual study participant data will be shared after anonymization upon study publication in an open data repository (e.g. DANS or Yoda).

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07421466
Lead sponsor
Wageningen University
Responsible party
Ciaran Forde (Prof. Dr., Wageningen University) — Principal investigator
First posted
Feb 19, 2026
Start date
Sep 15, 2025
Primary completion
Oct 21, 2025
Completion
Oct 21, 2025
Last update
Feb 19, 2026

Study contacts

Monica Mars, PhD
principal investigator · WUR
Ciaran Forde, PhD
principal investigator · Wageningen University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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