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Interaction of Salivary Proteins and Polyphenols

Interaction and Modulation of Salivary Proteins With Repeat Exposure to Polyphenols

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03501238
Enrollment
63
Registered
2018-04-18
Start date
2017-06-08
Completion date
2018-01-01
Last updated
2023-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diet Habit, Diet Modification, Taste, Altered, Saliva Altered

Brief summary

Participants will be chosen through an initial sensory test to find high and low-perceivers of astringency. Selected participants will drink a chocolate milk or milk substitute beverage for one week each with washout weeks in between. At the end of each week participants will taste and rate multiple beverages for their astringency and other sensory properties. Participants will provide saliva samples weekly for proteomic analysis and (potentially) analysis of polyphenols. Participants will also be asked to provide a 24 hour dietary recall once per week. Data will be analyzed to determine if there is a relationship between polyphenol exposure, astringency ratings, and salivary protein composition.

Interventions

Chocolate bovine milk will be consumed everyday for 1 week. Milks will be store-bought, with added sucrose and added cocoa powder.

OTHERChocolate milk substitute

Chocolate milk substitute will be consumed everyday for 1 week. Milks will be store-bought, with added sucrose and added cocoa powder.

OTHERChocolate milk substitute with gelatin

Chocolate milk substitute with gelatin added will be consumed everyday for 1 week. Milks will be store-bought, with added sucrose and added cocoa powder.

Sponsors

Purdue University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Masking description

Participants will not know the specifics of each beverage they are taking home.

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* High or low perceivers of astringency (from initial screening)

Exclusion criteria

* Current smokers (within 30 days), dairy/nut/cocoa allergies, piercings in mouth, mid-range perceiver of astringency, issues with taste, smell, swallowing or choking.

Design outcomes

Primary

MeasureTime frameDescription
Relative salivary proteins in saliva1 yearMeasure relative amounts of salivary proteins in participant saliva.

Secondary

MeasureTime frameDescription
Subject Diets8 monthsCollect participant 24 hour dietary recalls to generate data on eating patterns and dietary choices. Analyze correlations with saliva and sensory ratings. Dietary data that will be analyzed include measures such as: fruit and vegetable intake, fat intake (and type of fat). 24 hour recalls will be assess using the ASHA online tool, which collects data on all foods eaten in the last 24 hours.
Chocolate milk flavor ratings8 monthsMeasure subjects ratings for astringency, bitterness, sweetness, and liking for chocolate milk. A generalized visual analog scale will be used, ranging from 0 (None for intensity and Worst ever for liking) to 100 (Strongest ever for intensity and Best ever for liking).
Chocolate milk substitute flavor ratings8 monthsMeasure subjects ratings for astringency, bitterness, sweetness, and liking for chocolate almond milk. A generalized visual analog scale will be used, ranging from 0 (None for intensity and Worst ever for liking) to 100 (Strongest ever for intensity and Best ever for liking).
Chocolate milk substitute with gelatin flavor ratings8 monthsMeasure subjects ratings for astringency, bitterness, sweetness, and liking for chocolate almond milk with added gelatin. A generalized visual analog scale will be used, ranging from 0 (None for intensity and Worst ever for liking) to 100 (Strongest ever for intensity and Best ever for liking).
Polyphenol content in saliva samples8 monthsMeasure polyphenol content in expectorated subject saliva samples.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026