None listed
Conditions
Brief summary
Scientific evidence suggests that berry fruit-derived polyphenolic compounds can regulate the digestion, absorption and utilisation of sugar. This presents an opportunity for the development of blackcurrant foods that regulate sugar metabolism and energy production. We have gathered proprietary information on the composition and bioavailability of NZ blackcurrant fruits and derived products, and now turn our focus to how to explore how the ‘timed’ consumption of blackcurrants influences sugar metabolism to maximise energy production. In particular pilot study, we aim to explore the interactions between blackcurrant and sugar 1 hr post-consumption on sugar metabolism and energy production.
Interventions
This trial is aimed at assessing how ‘timed’ blackcurrant consumption influences sugar metabolism and energy production. The trial is a parallel design consisting of three trial arms. This design was selected since the influence of blackcurrant on sugar metabolism is currently unknown; a parallel trial design will eliminate any potential problems from a cross-over design. In all three trial arms, participants will be asked to fast for 12 hrs the night before and eat a set breakfast (One Square Meal Bar [Cookie Time Ltd.]) 2 hrs before the start of the trial. Participants will be randomised into 3 trial arms; arm 1 will consume a 200 mL drink containing fruit sugar (equivalent to the amount in the blackcurrant extract, i.e. for 2.2 g glucose, 2.6 g fructose, 0.36 g sucrose) diluted in water and then 1 hr later a 200 ml sugar drink containing 40 g sucrose diluted in water, arm 2 will consume a 200 ml fruit sugar drink (as described above) and then 1 hr later a blackcurrant / sugar drink (containing a whole blackcurrant extract equivalent to 3.2 mg polyphenolic compounds /Kg and 40 g sucrose) diluted in water, and arm 3 will consume a 200 mL blackcurrant drink (containing a whole blackcurrant extract equivalent to 3.2 mg polyphenolic compounds /Kg) diluted in water and then 1 hr later a 200 mL sugar drink containing 40 g sucrose diluted in water. The blackcurrant extract was commercially sourced from Sujon Berries (New Zealand) and the sugars purchased from Healtheries (New Zealand) and dinks were prepared under New Zealand food safety requirements. The trial will take place in designated clinical facilitates within PFR and will be conducted by experience trial co-ordinators, who are also First Aider and trained phlebotomist. The trial co-ordinator will monitor the welfare of participants and ensure that they adhere to trial arm protocols. Participants will be randomised into one of the trial three arms. In all three trial arms a small amount of blood (capillary samples) will be taken prior to the start of the trial, after the consumption fruit sugar, blackcurrant + / - sugar drinks and then 1 hr later at specific times over a 4 hr period; 0, 15, 30, 45, 60, 90, 120, 150, 180, 240 mins after the consumption of the sugar or blackcurrant/sugar drink.
Sponsors
Study design
Eligibility
Inclusion criteria
Healthy individuals (male or female) aged 16-60 years old. Individuals will be required to complete a health questionnaire and provide informed written consent
Exclusion criteria
Individuals will be excluded if they are unwilling or unable to provide informed written consent or comply with the study procedures. Participants will also be excluded if they have (i) known hypersensitivity or intolerance to blackcurrants or berry fruit-derived products, (ii) health conditions that may a ect their ability to regulate sugar digestion/absorption (i.e. diabetes, metabolic syndrome). In addition, participants will be excluded if they are pregnant or planning to get pregnant in the near future or have any of the following conditions: (i) blood borne diseases (e.g. hepatitis), (ii) clinically diagnosed high/low blood pressure, (iii) recent bacterial or vial illness, (iv) are taking any mediation that a ects the properties of blood (e.g. blood clotting). Furthermore, potential volunteers will be excluded if they have donated blood within 4 weeks from the start of the study.