Actively Recruiting
Interaction Between White Potato Consumption and Meal Timing on Glycemic Response and Appetite in Adults
Led by Toronto Metropolitan University · Updated on 2025-11-17
30
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
Sponsors
T
Toronto Metropolitan University
Lead Sponsor
A
Alliance for Potato Research and Education
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the interaction between white potato consumption and meal timing on glycemic response, subjective appetite, and energy intake in adults. The investigators hypothesize that white potatoes will modulate glycemic response, enhance satiety, and mitigate subsequent meal consumption and overall food intake when compared with meals containing low glycemic carbohydrates. Furthermore, they anticipate that the timing of white potato consumption will yield differential effects, with breakfast consumption exerting a more pronounced impact on satiety and subsequent food intake reduction compared to dinner consumption.
CONDITIONS
Official Title
Interaction Between White Potato Consumption and Meal Timing on Glycemic Response and Appetite in Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 65 years
- Healthy body weight with body mass index (BMI) between 18.5 and 24.9 kg/m2
You will not qualify if you...
- Previous diagnosis of diabetes or gastrointestinal, liver, or kidney disease
- Major medical or surgical event within the past 6 months
- Significant weight change in the past 6 months
- Taking medication that could affect study measurements
- On a diet within the past 6 months
- Skip breakfast or unable to consume test treatment food
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Centre for Urban Innovation (CUI-109), School of Nutrition, Toronto Metropolitan University
Toronto, Ontario, Canada, M5B2K3
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
6
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