Skip to content

Evaluate the Link Between the Characteristics of Oral Physiology and the Formation of the Food Bolus During the Consumption of Dairy Products in Elderly People

Evaluate the Link Between the Characteristics of Oral Physiology and the Formation of the Food Bolus During the Consumption of Cheese Products in Elderly People

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03227913
Acronym
AlimaSSenSLait
Enrollment
80
Registered
2017-07-24
Start date
2016-07-28
Completion date
2017-09-30
Last updated
2017-07-24

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

Conditions

Old Person

Brief summary

The aim of this study is to understand how dairy products enriched in minerals and proteins are broken down in the mouth. More specifically, investigators wish to evaluate the link between oral physiology (salivation and mastication) and formation of the food bolus during the consumption of enriched cheese, that is to say the way in which the food is broken down to be swallowed. The study will take place at the INRA in Dijon during 2 one-hour sessions spread over 4 months. These two sessions will allow investigators to characterise the chewing behaviour of the subjects and their salivation, and the structure of the food bolus formed when eating the four products of the project. For each of the four foods in each session: * Two samples of saliva will be taken * A video will be made of subjects eating one of the study products * Subjects will chew the study foods and spit them out.

Interventions

1. Without stimulation: the first will be used to measure the flow of naturally secreted saliva 2. With stimulation: the second will will be used to measure the flow and viscosity of the saliva secreted after stimulation

Measure the time taken by subjects to chew the food and the number of bites they use before swallowing

* Analysis by a compression and viscosity test * Evaluation of the quantity of saliva incorporated by drying

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Persons who have provided written consent * Age ≥ 65 years old * Persons living at home * Persons who can travel independently

Exclusion criteria

* Adults under guardianship * Persons without health insurance cover * Persons in hospital * Persons in institutions * Persons whose Mini-Mental State Examination (MMSE) is \< 24 * Persons requiring enteral or parenteral nutrition * Persons who in the previous 12 months received € 4500 for taking part in clinical trials, including the present study * Persons in a period of exclusion of a previous study * Food allergies (dairy products in particular)

Design outcomes

Primary

MeasureTime frame
Duration of chewingChange from baseline at 4 months
Frequency of chewingChange from baseline at 4 months
Rheology testChange from baseline at 4 months
calculation of insanity rateChange from baseline at 4 months

Countries

France

Contacts

Primary ContactPatrick MANCKOUNDIA
patrick.manckoundia@chu-dijon.fr3 80 29 39 70

Outcome results

None listed

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