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Oral Processing and Appetite in Older Adults

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University of Reading

Status

Completed

Conditions

Appetitive Behaviour
Older Adults
Oral Processing
Food Intake

Study type

Observational

Funder types

Other

Identifiers

NCT05671003
UREC 22/29

Details and patient eligibility

About

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).

Full 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.

Enrollment

88 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial contacts and locations

1

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Central trial contact

Lisa Methven, BSc, PhD; Miriam Clegg, BSc, PhD

Data sourced from clinicaltrials.gov

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