ClinicalTrials.gg
CompletedNCT05591612Updated Aug 1, 2024

Increasing Vegetable Intake Using Monosodium Glutamate: A Reduced-Effort Intervention

An interventional study of Salt replacement seasoning (50% salt and 50% MSG) mix and Salt replacement seasoning (70% salt and 30% MSG) mix in Healthy Nutrition, Culinary Medicine and Sodium Excess, sponsored by Texas Tech University. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-01.

Sponsored by Texas Tech University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
148
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Food Intake Study: This will be a 4-week randomized controlled intervention study with a vegetable intake questionnaire, daily food intake, and seasoning usage measurement to test the acceptability of different seasoning ingredients and vegetable intake in healthy adults. Participants will be randomly assigned to one of three groups (a) vegetables prepared with 50% NaCl and 50% MSG (50/50MSG Mix); (b) vegetables prepared with 70% NaCl and 30% MSG (70/30 MSG Mix); (c) vegetables prepared with NaCl (table salt).

Sensory Evaluation Study: A sensory evaluation utilizing all seasoning methods from the intervention will be conducted at a Texas Tech University culinary education lab. In a Texas Tech University culinary education lab, 2-4 vegetables will be cooked and seasoned with either 50/50MSG Mix, 70/30 MSG Mix, or NaCl for taste testing. Then, using a standardized form, participants will rate their acceptability and preference of each vegetable, including sensory characteristics such as appearance, color, odor, texture, and flavor.

Read the detailed description

Food Intake Study: This will be a 4-week randomized controlled intervention study with a vegetable intake questionnaire, daily food intake, and seasoning usage measurement to test the acceptability of different seasoning ingredients and vegetable intake in healthy adults. Participants will be randomly assigned to one of three groups (a) vegetables prepared with 50% NaCl and 50% MSG (50/50MSG Mix); (b) vegetables prepared with 70% NaCl and 30% MSG (70/30 MSG Mix); (c) vegetables prepared with NaCl (table salt). Before the intervention, each group will be asked to keep a daily food intake record for one week to determine baseline vegetable intake. Each group will receive a culinary medicine program electronically, including recipe demonstrations, cooking skills, and nutrition education videos to provide instruction for vegetable consumption according to the Dietary Guidelines for Americans. According to each treatment group, a bottle of seasoning ingredients will be provided to use on vegetables. Prior to the intervention, participants will be 1) instructed on how to track daily food intake data using the MyFitnessPal® app, 2) track food intake for seven days, and 3) complete a questionnaire regarding vegetable intake pre-intervention. According to the group assignment, each treatment group will also receive a bottle of a seasoning blend that includes either 50/50MSG Mix, 70/30 MSG Mix, or NaCl to use on vegetables prepared at home. According to the Dietary Guidelines for Americans, culinary medicine education (recipe demonstrations, cooking skills, and education videos for vegetable consumption) will be delivered electronically at baseline and once per week for four weeks to each participant. For four weeks, participants will track all meals daily, including vegetables prepared with designated seasoning at home. Remote follow-ups and dietary intake will be conducted weekly. After the intervention, the participants will 1) complete the same vegetable intake questionnaire for the four weeks of the intervention and 2) return the bottle of seasoning blend provided. Usage of seasoning for four weeks will be recorded. Data analyses will evaluate the changes in outcomes within and between groups. Participants will also be informed of the sensory evaluation study to be included among other participants of that study. MSG_Diet Food Questionaries (Updated).docx MyFitness Pal instructions.docx

Sensory Evaluation Study: A sensory evaluation utilizing all seasoning methods from the intervention will be conducted at a Texas Tech University culinary education lab. In a Texas Tech University culinary education lab, 2-4 vegetables will be cooked and seasoned with either 50/50MSG Mix, 70/30 MSG Mix, or NaCl for taste testing. Then, using a standardized form, participants will rate their acceptability and preference of each vegetable, including sensory characteristics such as appearance, color, odor, texture, and flavor.

02

Conditions studied

  • Healthy Nutrition
  • Culinary Medicine
  • Sodium Excess

Browse trials for

03

In context

Hypernatremia

49 studies on the registry are indexed under Hypernatremia; 8 are open to participants now.

This study's enrollment of 148 is above the median of 64 across 32 interventional studies indexed under Hypernatremia.

Browse Hypernatremia studies →

Lead sponsor

Texas Tech University is the lead sponsor of 82 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18 years old and above

Exclusion criteria

Exclusion Criteria:

  • Allergy or aversion to MSG (monosodium glutamate) or potassium chloride
  • Those that do not have a smart phone with the ability to download an app.
  • Those who do not have a full kitchen and the willingness and ability to prepare vegetables according to a recipes.
  • Those with an allergy, aversion, or dislike to vegetables that would make them not consume any vegetables during the study
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
148 participants (actual)

Study arms

  • Experimental
    50% NaCl and 50% MSG Seasoning Mix

    Participants received cooking demonstrations and nutrition education, and were asked to use the seasoning provided (50% NaCl and 50% MSG Seasoning Mix) on vegetables and foods prepared. Then they recorded their food intake to compare vegetable intake to other groups.

    Behavioral: Salt replacement seasoning (50% salt and 50% MSG) mix

  • Experimental
    70% NaCl and 30% MSG Seasoning Mix

    Participants received cooking demonstrations and nutrition education, and were asked to use the seasoning provided (70% NaCl and 30% MSG Seasoning Mix) on vegetables and foods prepared. Then they recorded their food intake to compare vegetable intake to other groups.

    Behavioral: Salt replacement seasoning (70% salt and 30% MSG) mix

  • Experimental
    NaCl seasoning

    Active Control Participants received cooking demonstrations and nutrition education, and were asked to use table salt on vegetables and foods prepared. Then they recorded their food intake to compare vegetable intake to other groups.

    Behavioral: NaCl (sodium chloride/table salt)

Interventions

  • BehavioralSalt replacement seasoning (50% salt and 50% MSG) mix

    Individuals in this group were provided a seasoning that replaced 50 % regular salt with a reduced-sodium MSG substitute. This study assessed the vegetable intake using the intervention of 50/50 MSG Mix to be added to vegetables in diet.

  • BehavioralSalt replacement seasoning (70% salt and 30% MSG) mix

    Individuals in this group were provided a seasoning that replaced 30 % regular salt with a reduced-sodium MSG substitute. This study assessed the vegetable intake using the intervention of 70/30 MSG Mix to be added to vegetables in diet.

  • BehavioralNaCl (sodium chloride/table salt)

    Individuals in this group were asked to use normal seasoning of regular salt. This study assessed the vegetable intake using table salt to be added to vegetables in diet.

06

What researchers measure

Primary outcomes

  1. Vegetable Intake

    To assess the consumption of vegetables by the participant measured by data from self-recorded diet as entered in smart phone application (My Fitness Pal©).

    Time frame: 5 weeks

Secondary outcomes

  1. Vegetable Palatability

    Preference Test Preference Test Scale * Scale Title: Likert Scale for Vegetable Preference * Minimum Value: 1 (indicating "dislike extremely") * Maximum Value: 9 (indicating "like extremely") * Higher Scores Indicate: A better outcome, meaning higher scores reflect a greater preference for the vegetables seasoned with the various NaCl/MSG mixtures.

    Time frame: day one (15 minutes)

  2. Vegetable Palatability

    Triangle Sensory Evaluation Test Triangle Test Scale * Scale Title: Confidence Scale for Triangle Test * Minimum Value: 1 (indicating "not confident") * Maximum Value: 5 (indicating "completely confident") * Higher Scores Indicate: A better outcome in terms of confidence level in identifying the odd sample out. Higher scores reflect greater confidence in distinguishing between the NaCl/MSG mixtures and pure NaCl.

    Time frame: day one (15 minutes)

  3. Seasoning Usage

    Determine which group used the most seasoning Each group will be provided a bottle of seasoning. It will be weighed prior to them taking the seasoning. The participants will be asked to bring the remaining seasoning back to weight to determine the amount of seasoning usage during the 4 week study. Usage of seasoning for four weeks will be recorded.

    Time frame: 5 weeks

07

Study locations

1 site
  • Nutrition and Metabolic Health Initiative
    Lubbock, Texas 79410, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05591612
Lead sponsor
Texas Tech University
Collaborators
American Society for Nutrition
Responsible party
Sponsor
First posted
Oct 24, 2022
Start date
Feb 10, 2023
Primary completion
Nov 15, 2023
Completion
Nov 15, 2023
Last update
Aug 1, 2024

Study contacts

Shannon Galyean, PhD
principal investigator · Texas Tech University

Oversight

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

Not currently enrolling

This study is completed, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion