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Clinical Trials/NCT05671003
NCT05671003
Completed
Not Applicable

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

University of Reading1 site in 1 country88 target enrollmentJanuary 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Older Adults
Sponsor
University of Reading
Enrollment
88
Locations
1
Primary Endpoint
Objective appetite assessment: Ad-libitum meal consumption
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 15, 2023
End Date
September 15, 2023
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Miriam Clegg

Associate Professor

University of Reading

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Objective appetite assessment: Ad-libitum meal consumption

Time Frame: During the procedure

Consumption of the ad-libitum meal is measured (g). Participants are instructed to eat until they feel comfortable full

Secondary Outcomes

  • BMI(During the procedure)
  • Oral Health(During the procedure)
  • Subjective appetite assessment: VAS(During the procedure)
  • Salivary a-amylase(During the procedure)
  • Salivary flow rate(During the procedure)
  • Glucose(During the procedure. Every 15 minutes for the first hour after the meal and every 30 minutes thereafter till the end of the total 3 hours)
  • Gastric Emptying(During the procedure)
  • Chewing rate(During the procedure)
  • Chewing ability(During the procedure)
  • Insulin(During the procedure. Every 15 minutes for the first hour after the meal and every 30 minutes thereafter till the end of the total 3 hours)

Study Sites (1)

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