SweetSpot - The Effect of Non-nutritive Sweeteners on Health
Recruiting
N/AInterventional Study
Healthy Adult
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
45 – 79
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
60 (estimated)
Sponsor
Wageningen University · Other
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
The aim of the study is to investigate the effect of non-nutritive sweeteners on glucose regulation. Secondary objectives are to investigate the effect of NNS on gut microbiome, gut hormone secretion, sweet taste sensitivity and preference, and the excretion of NNS in urine.
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Eligibility Criteria
Inclusion Criteria:
* Age 45-79 years;
* BMI of 20-35 kg/m2;
* Having veins suitable for placement of a venflon catheter.
Exclusion Criteria:
* Diseases or prior surgeries affecting the stomach, liver, kidneys or intestines (allowed i.e. appendectomy);
* Cardiovascular diseases (e.g. heart failur…
Inclusion Criteria:
* Age 45-79 years;
* BMI of 20-35 kg/m2;
* Having veins suitable for placement of a venflon catheter.
Exclusion Criteria:
* Diseases or prior surgeries affecting the stomach, liver, kidneys or intestines (allowed i.e. appendectomy);
* Cardiovascular diseases (e.g. heart failure) or cancer (e.g. non-invasive skin cancer allowed);
* Diagnosed with type 1 or type 2 diabetes;
* Drug treated thyroid diseases (well substituted hypothyroidism is allowed for inclusion);
* HbA1c level \>6.5% (\>48 mmol/mol), as measured during the screening visit;
* Anaemia defined as Hb concentrations \<8.5 mmol/L for men and \<7.5 mmol/L for women via finger prick;
* Regular use of/receiving medication interfering with research outcomes (as judged by research physician), such as use of glucose lowering drugs, insulin, or use of medication that impacts the gastro-intestinal system;
* Use of antibiotics over the last 3 months before study start;
* Donated blood within 2 months prior to the screening;
* Food allergies, intolerances (including lactose/gluten intolerance) for products used in the study design and/or dietary restrictions interfering with the study (including special diets and eating disorders);
* Followed a diet that can interfere with the study outcomes within 1 month prior to the screening (e.g. ketogenic, sugar free, carbohydrate free);
* Not willing to eat all products in the study diet, including eggs and dairy. Vegetarian is possible;
* Not willing to consume non-nutritive sweeteners;
* Not willing to quit the use of supplements that can interfere with the study outcomes (e.g. pre- or probiotics).
* Intention to change the intensity of exercise during the study period or planning to join a intensive sport event (e.g. marathon or triathlon);
* Intention to lose or gain weight;
* Working night shifts regularly;
* Smoking regularly
* Use of soft and/or hard drugs (cannabis included);
* Abuse of alcohol (defined as \>14 glasses (women) or \>21 glasses (men) of alcoholic beverages per week);
* Being pregnant or lactating or planning to become pregnant;
* Inability to understand study information and/or communicate with staff;
* Participation in another study that involves an intervention within two months prior to the intervention;
* Working or doing a thesis/internship at the division of Human Nutrition \& Health, or the Food, Health \& Consumer Research group of Wageningen Food \& Biobased Research.
Contacts
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