Healthy Clinical Trial
— AMOREOfficial title:
Gastrointestinal and Blood Glucose Responses to Breakfast Porridges Made From Different Grains: A Magnetic Resonance Imaging Pilot Study in Healthy Volunteers
Breakfast porridges are made from milled grains and are commonly eaten worldwide.
Traditionally different grains are used in different countries. For example, oats are more
common in the Anglo-Saxon countries; rye is favoured in the Scandinavian countries whilst
millet is very common in parts of India and Africa. However the nutritional value and
potential metabolic and health effects may vary dramatically between different grains. For
example what is the effect of the different grains on blood sugar or on how fast the stomach
empties after eating the porridge and how full people feel. All these physiological
responses may differ between these grains resulting in potential health benefits.
RESEARCH QUESTION: The investigators hypothesise that porridges made from different grains
will behave differently during the digestion and cause differences in blood glucose levels,
gastric emptying and appetite.
This study, which is a 4-way, randomized, cross over pilot study in healthy participants,
aims to answer this research question.
The participants will be asked to eat a porridge breakfasts made with oats, rye and millet
of different varieties (but containing the same amount of calories), in 4 morning studies
one week apart. MRI will be used to monitor the gastrointestinal fate of the breakfasts and
measure gastric emptying using MRI, blood glucose levels using a finger prick test and
self-reported appetite scores.
| Status | Completed |
| Enrollment | 16 |
| Est. completion date | May 2016 |
| Est. primary completion date | March 2016 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Aged 18-65 - Body mass index (BMI) = 18.0 and = 30.0 kg/m2 - Able to give informed consent - Apparently healthy: no medical conditions which might affect study measurements (judged by study physician) Exclusion Criteria: - Use of medication which interferes with study measurements (as judged by the study physician). - Participation in another nutritional or biomedical trial 3 months before the pre-study examination or during the study. - Not used to eating breakfast - Not used to eating three meals a day - Reported participation in night shift work during the two weeks prior to pre-study investigation or during the study. Night work is defined as working between midnight and 6.00 AM. - Strenuous exercise for more than10 hours per week. - Consumption of =21 alcoholic drinks in a typical week - Reported weight loss or gain = 10 % of bodyweight during the six months period before the pre-study examination. - Following a medically- or self-prescribed diet during the two weeks prior to the pre-study examination and until the end of the study - Dislike of the products served as the dietary test treatments - Any allergy or food intolerance to the test treatments - An eating disorder as indicated by the Three factor eating questionnaire - Not suitable for MRI scanning (e.g., presence of metal implants, infusion pumps and pacemakers) as assessed by standard MRI safety questionnaire. - Pregnancy declared by candidate - Antibiotic or prescribed probiotic treatment in the past 12 weeks - Inability to lie flat - Exceeding the scanner bed weight limit of120kg - Poor understanding of the spoken and/or written English language |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Nottingham Digestive Disases Centre | Nottingham | Nottinghamshire |
| Lead Sponsor | Collaborator |
|---|---|
| University of Nottingham |
United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Time to peak of blood glucose | Time to peak of post prandial blood glucose, measured using finger prick method, up to 2h (AUC2h) postprandially | From baseline up to 2 hours postprandially | No |
| Other | Appetite VAS | Area Under the Curve for appetite (Fullness, Hunger, Prospective food consumption) post prandial 100 mm VAS scores AUC2h and AUC 3h | From baseline up to 3 hours postprandially | No |
| Other | Small bowel water content | Area Under the Curve of post prandial small bowel water content, measured by MRI, up to 2h (AUC2h) postprandially | From baseline up to 2 hours postprandially | No |
| Other | Food diaries | Records of all food eaten on the study day beyond the breakfast porridge provided in the morning | From 12:00 hours to 22:00 hours on the study day | No |
| Other | Correlations between blood, MRI and satiety data | Exploratory correlations between blood, MRI and satiety data | From baseline up to 2 hours postprandially | No |
| Primary | Blood glucose level | Area Under the Curve of post prandial blood glucose, measured using finger prick method, up to 2h (AUC2h) postprandially | From baseline up to 2 hours postprandially | No |
| Secondary | Gastric volumes | Area Under the Curve of post prandial gastric volumes, measured by MRI, up to 2h (AUC2h) postprandially | From baseline up to 2 hours postprandially | No |
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