The Chocolate Almond Study - Relating Chewing to Satiation and Postprandial Response

Recruiting N/A Interventional Study
Satiation, Satiety Postprandial Glycemia Postprandial Lipemia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 45
Sex
Female
Study type
Interventional
Purpose
Basic Science
Participants needed
35 (estimated)
Sponsor
University of Guelph · Other
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About This Trial
The goal of this clinical trial is to relate chewing behaviours to food intake and postprandial response for a texturally complex food matrix (almonds in white chocolate) in healthy young females. The main questions it aims to answer are: * Does the presence or preparation of almonds (whole versus chopped) influence satiation, i.e., the amount consumed at an ad libitum meal? * What is the correla…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * BMI between 18.5-27.9 kg/m\^2 or waist circumference less than 88 cm * No known food allergies or sensitivities * Non-restrained eaters based on the Three Factor Eating Questionnaire * No history of gastrointestinal diseases that may interfere with eating behaviour or digestio…
Contacts

Amanda J Wright, PhD

519-824-4120

ajwright@uoguelph.ca

CONTACT