Status:
COMPLETED
Glycemic and Satiety Response Study of Fibre-Enriched Pudding Products
Lead Sponsor:
University of Guelph
Collaborating Sponsors:
Ontario Ministry of Agriculture, Food and Rural Affairs
Natural Sciences and Engineering Research Council, Canada
Conditions:
Type 2 Diabetes Mellitus
Eligibility:
All Genders
18-70 years
Phase:
NA
Brief Summary
The purpose of this study is to determine the specific properties of a variety of dietary fibres that lead to different postprandial glycemic and satiety responses in individuals at risk for type 2 di...
Detailed Description
The purpose of this study is to determine the specific properties of a variety of dietary fibres that lead to different postprandial glycemic and satiety responses in individuals at risk for type 2 di...
Eligibility Criteria
Inclusion
- Men/Women
- Age 18-70 years
- CANRISK Questionnaire score ≥21 (brief questionnaire that identifies risk of diabetes)
- BMI ≥25 and \<40 kg/m2
- Prior use of acetaminophen
Exclusion
- Smokers
- Food allergies or any life-threatening allergy (food or otherwise)
- Acetaminophen allergy
- Gastrointestinal conditions or illnesses (Including, but not limited to, lactose intolerance, Celiac, Crohn's, Ulcerative Colitis (UC), Irritable Bowel Disorder (IBD))
- Serious major medical condition (i.e. renal, liver)
- Pregnant or breastfeeding
- Food Neophobia Scale score between 30 and 54 (Food Neophobia Scale is a questionnaire which is intended to screen out individuals who are unsure of consuming new products)
- TFEQ-CR \>16 (TFEQ is a questionnaire to screen for restrained eaters)
- Alcohol consumption\>4 drinks/sitting
- Medication or natural health products (NHPs) used for diabetes (glycemic control)
- Medication or NHPs contraindicated with acetaminophen
- Recent or intended significant weight loss or gain (i.e. \>4 kg in previous 3 months)
Key Trial Info
Start Date :
November 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2015
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT02289612
Start Date
November 1 2014
End Date
October 1 2015
Last Update
May 8 2018
Active Locations (1)
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1
Human Nutraceutical Research Unit
Guelph, Ontario, Canada, N1G 2W1