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Innovation of Breakfast Cereals and Snacks for Control of Appetite and Post-Prandial Glycemia

Innovation of Breakfast Cereals and Snacks for Control of Appetite and Post-Prandial Glycemia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02465021
Enrollment
30
Registered
2015-06-08
Start date
2015-03-31
Completion date
2015-10-31
Last updated
2017-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes, Obesity

Keywords

Satiety, Food intake, Breakfast cereals/snacks, Postprandial glycemia

Brief summary

The goal of the proposed research is to investigate the effects of novel snack products differing in macronutrient composition, fibre and sugar content on post-prandial glycemia and short-term appetite control in healthy adults.

Interventions

OTHERDietary intervention

All arms are given to all participants, in a randomized order

Sponsors

General Mills
CollaboratorINDUSTRY
University of Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy, non-smoking individuals aged 18-55 years with a body mass index of 20.0-29.9 kg/m2

Exclusion criteria

* Smokers, individuals with diabetes or other cardiometabolic diseases, persons who suffer from gastrointestinal disorders or have had gastric surgery, or people who regularly use bulk laxatives * Women with irregular menstruation or who use hormonal contraceptives or hormone replacement therapy * Individuals who regularly skip breakfast, have allergies to any of the test food ingredients, or who follow a restrictive diet

Design outcomes

Primary

MeasureTime frameDescription
Food intake120 minutesFood intake (kCal) is assessed 120 min after consumption of the treatments, using an ad libitum pizza lunch design. Participants are asked to eat, during a 20-min period, until feeling comfortably full

Secondary

MeasureTime frameDescription
Perceived satiety120 minutesSatiety scores (mm) are assessed using 100-mm Motivation to Eat visual analog scale questionnaires. A composite score of the four appetite questions, including Desire to Eat, Hunger, Fullness and Prospective Food Consumption, in the Motivation to Eat visual analog scale is calculated to obtain the average appetite score for statistical analysis
Blood glucose0 to 120 min (pre-ad libitum lunch) and 140 to 260 min (post-ad libitum lunch) after consumption of treatmentsBlood glucose (mmol/L) is measured using finger prick capillary blood samples
Blood insulin0 to 120 min (pre-ad libitum lunch) and 140 to 260 min (post-ad libitum lunch) after consumption of treatmentsBlood insulin (μU/mL) is measured using finger prick capillary blood samples

Other

MeasureTime frameDescription
Food Recall24 hoursParticipants are asked to complete a 24-hour Food Recall starting at dinner the night before each study session and ending at dinner the day of that session.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026