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Study identifier: NCT07065461 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Satiation, Satiety · Postprandial Glycemia · Postprandial Lipemia  ·  Sponsor: University of Guelph

PhaseNA
Planned participants35
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersYes

About this study

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 correlation between chewing behaviour, satiation, and changes in postprandial glucose, triacylglycerols, and satiety ratings? Participants will attend the research centre fasted on three occasions to consume an ad libitum meal, complete questionnaires, and provide fasting and postprandial finger prick blood samples.

This description comes directly from the study's public registry record.

Talk to the study team

Amanda J Wright, PhD  ·  519-824-4120  ·  ajwright@uoguelph.ca

Always discuss trial participation with your own doctor first.

Locations (1)

Department of Human Health SciencesGuelph, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07065461