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Oral Processing and Appetite in Older Adults

The Effect of Dentition, Eating Rate, Oral Processing, and Gastric Emptying on Appetite and Satiety in Older Adults (≥65 Years of Age)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05671003
Enrollment
88
Registered
2023-01-04
Start date
2023-01-15
Completion date
2023-09-15
Last updated
2024-07-05

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

Conditions

Appetitive Behaviour, Food Intake, Older Adults, Oral Processing

Keywords

older adults, appetite, oral processing, food intake, chewing, salivary flow, gastric emptying

Brief summary

The goal of this observational study is to learn about changes in oral processing and appetite in older adults aged 65+ years old. The main question it aims to answer is if oral processing affects gastric emptying in older adults (≥65 years old).

Detailed description

* To investigate if food intake and satiety differ between faster and slower eaters, within older adults (≥65 years old). * To assess if chewing rate, salivary flow rate, oral processing and gastric emptying differ between older adults (≥65 years old) with smaller versus bigger appetites.

Interventions

None listed

Sponsors

University of Bern
CollaboratorOTHER
Wageningen University
CollaboratorOTHER
Queen's University, Belfast
CollaboratorOTHER
University of Reading
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* 65 years old or over (no upper age limit);each group will contain an equal number of male and female participants; * living sufficiently local to attend the two visits needed; * able to understand and communicate in English language.

Exclusion criteria

* Diagnosed dysphagia; * (recent) oral surgery that significantly affects eating and/or swallowing; * diagnosis of type 1 or type 2 diabetes; * participant undergoing current treatment for cancer; * participants with zero natural teeth; * severe loss of appetite and not able to finish a meal (based on CNAQ) and/or people on special or therapeutic diets that restrict the consumption of a full meal and/or the meals provided; * not able to provide informed consent as defined by the T-CogS test (participants with T-CogS \< 22 will be excluded); * participants having a pacemaker; * not able to accept the two meal dishes provided and/or relevant food/ingredient included in the meals allergies or intolerances or aversions; * not able to feed themselves.

Design outcomes

Primary

MeasureTime frameDescription
Objective appetite assessment: Ad-libitum meal consumptionDuring the procedureConsumption of the ad-libitum meal is measured (g). Participants are instructed to eat until they feel comfortable full

Secondary

MeasureTime frameDescription
Gastric EmptyingDuring the procedureGastric emptying is measured using of 100 microliters of 13C Octanoic Acid breath test
Chewing rateDuring the procedureChewing rate would be assessed with recording the preload breakfast meal provided and analysing the video recording in software (ELAN 6.4) for number of chews, bites, swallows, time of food in the mouth.
Salivary flow rateDuring the procedureStimulated and unstimulated salivary flow rate would be assessed with passive drooling method.
BMIDuring the procedureBMI is assessed by using a body composition monitor (OMRON Viva)
Subjective appetite assessment: VASDuring the procedureAppetite are assessed using a 100 mm Visual Analogue Scales (VAS, scale 0-100)
Chewing abilityDuring the procedureChewing ability will be assessed by using a colour mixing ability chewing gum test (Heu-Check test, University of Bern)
GlucoseDuring the procedure. Every 15 minutes for the first hour after the meal and every 30 minutes thereafter till the end of the total 3 hoursGlucose will be assessed from finger prick blood samples
InsulinDuring the procedure. Every 15 minutes for the first hour after the meal and every 30 minutes thereafter till the end of the total 3 hoursInsulin will be assessed from finger prick blood samples
Salivary a-amylaseDuring the procedureSalivary a-amylase activity will be assessed from the stimulated saliva collected, by using a-amylase kinetic kit
Oral HealthDuring the procedureOral Health will be assessed by using an Oral Health Questionnaire

Countries

United Kingdom

Outcome results

None listed

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