- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03769389
Assessing the Glycaemic Index of Two Different Cultivars of Date Fruit
Assessing the Glycaemic Index of Two Different Cultivars of Date Fruit When Mixed With 0% Fat Yogurt on Healthy Volunteers.
Fruit of the date palm (P. dactylifera) may be considered as an emerging and potential candidate for the development of health-promoting foods, owing to its high nutritional values.
Furthermore, aqueous extracts of dates have previously been shown to have potent antioxidant activity, because they inhibit in vitro lipid and protein oxidation and possess free radical scavenging capacity.
Although the high sugar content of date fruit has always been a concern, date fruit has been regarded as a low-GI to medium-GI food. However, very limited, inconsistent and contradictory information is available on the glycaemic index values of different date varieties, which may be attributed to both the methodology as well as other food factors. Date consumption is high among people of Arabic origin, where it's very common for them to be eaten with coffee or yoghurt. Therefore, in view of these concerns, the objective of this trial is to evaluate the glycaemic response of two different varieties of dates, named Birhi & Khassab, in an early maturation stage (Rutab stage), when mixed with 0% fat yogurt, on ten healthy participants aged between 18 and 45.
Study Overview
Status
Intervention / Treatment
Detailed Description
Introduction Although, the fruit of the date palm (P. dactylifera) may be considered an emerging and potential candidate for the development of health-promoting foods owing to its high nutritive values,the high sugar content of date fruit has always been a concern. Sun-dried dates, which is the well-known ripening stage of date fruit, can be regarded as low-GI to medium-GI food. However, very limited, inconsistent and contradictory information is available on the glycaemic Index values of different date varieties. This variation could be attributed to either the methodology or the food factors.
Rational and objective Nowadays, low-GI foods have often been found to induce beneficial effects on risk factors for certain non-communicable chronic diseases . As the chemical composition of dates can vary depending on cultivar, soil conditions, agronomic practices as well as the ripening stage. It is important to know the GI of the local/regional date varieties, and in different date products such as dates with yoghurt. Date consumption is high among people of Arabic origin, where it is very commonly eaten with coffee or yoghurt. During the first trial of this PHD project, treatments containing 150g of 0% fat yoghurt and two different freeze dried date powders, depending on if it was a Birhi treatment or Khassab treatment, were formulated. These were used to assess acute effects of date fruit and yoghurt on mood and cognitive performance in healthy volunteers, as per the ethical approval from Newcastle University. These exact treatments will be used again, and the trial will aim to evaluate their glycaemic index on 10 healthy participants.
Participants Ten healthy participants aged between 18 and 45 will be recruited. Participants will be required to undergo a screening visit, followed by three study visits, which will last 2:15 minutes for each visit. Glycaemic indexes will be calculated using standard methods. Results will be calculated using means and standard deviations.
Design
A standard experimental study involving the measurement of the glycaemic responses of the ingestion of two different varieties of dates, when mixed with 0% fat yoghurt, and a placebo treatment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Tyne And Wear
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Newcastle upon Tyne, Tyne And Wear, United Kingdom, NE1 7RU
- NU-Food Research Facility
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants A total of 10 healthy participants aged between 18 and 45 will be recruited through advertisement via poster and flyer. This is an internationally recognised standard protocol which recommends using 10 volunteers or replicates for each foodstuff, and all participants will be required to undergo a screening visit.
Inclusion Criteria Healthy participants aged 18-45 with a BMI >18 <36 will be recruited from the Newcastle Upon-Tyne area.
Exclusion Criteria:
Participants will be considered ineligible to participate in the study if they meet any of the following criteria:
- They have any metabolic diseases such as type 1 or type 2 diabetes.
- They have a BMI above 35kg/m2 or lower than 18kg/m2
- They are taking any illicit or prescribed drugs.
- They are using dietary supplements, over the counter medicine or recreational drugs
- They are females who are pregnant or seeking to become pregnant.
- They have allergies to any food products.
- They have any dairy intolerances.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: BASIC_SCIENCE
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: assessing the GI + GL of Birhi + YEO 0% fat yoghurt
47g of total carbohydrate in which contains 43.6g of Freeze-dried of Birhi powder+ 150g of 0% fat yoghurt
|
Birhi which contain the following: 43.6g of Freeze-dried date powder+ 150g of 0% fat yoghurt
34.6g of freeze-dried date powder+ 150g of 0% fat yoghurt
50g of pure glucose dissolved in 100ml of water
|
|
EXPERIMENTAL: assessing the GI + GL of Khassab + YEO 0% fat yoghurt
47g of total carbohydrate in which contains34.6g of freeze-dried Khassab powder+ 150g of 0% fat yoghurt
|
Birhi which contain the following: 43.6g of Freeze-dried date powder+ 150g of 0% fat yoghurt
34.6g of freeze-dried date powder+ 150g of 0% fat yoghurt
50g of pure glucose dissolved in 100ml of water
|
|
EXPERIMENTAL: assessing the GI + GL of 50g of Glucose in 100 ml of water
50g of pure glucose dissolved in 100ml of water
|
Birhi which contain the following: 43.6g of Freeze-dried date powder+ 150g of 0% fat yoghurt
34.6g of freeze-dried date powder+ 150g of 0% fat yoghurt
50g of pure glucose dissolved in 100ml of water
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood glucose concentrations (mml/15 min)after the consumption Birhi
Time Frame: Change from baseline BG level at minute 15,30,45,60,75,90,105, 120 post dose
|
On each of the study days, blood glucose will be measured at baseline, 15 min post-dose, 30 min post-dose, 45 min post-dose, 60 min post-dose, 75 min post-dose, 90 min post-dose, 105 min post-dose and 120 min post- dose.
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Change from baseline BG level at minute 15,30,45,60,75,90,105, 120 post dose
|
|
Blood glucose concentrations (mml/15 min)after the consumption Khassab
Time Frame: Change from baseline BG level at minute 15,30,45,60,75,90,105, 120 post dose
|
On each of the study days, blood glucose will be measured at baseline, 15 min post-dose, 30 min post-dose, 45 min post-dose, 60 min post-dose, 75 min post-dose, 90 min post-dose, 105 min post-dose and 120 min post- dose.
|
Change from baseline BG level at minute 15,30,45,60,75,90,105, 120 post dose
|
|
Blood glucose concentrations (mml/15 min)after the consumption Placebo
Time Frame: Change from baseline BG level at minute 15,30,45,60,75,90,105, 120 post dose
|
On each of the study days, blood glucose will be measured at baseline, 15 min post-dose, 30 min post-dose, 45 min post-dose, 60 min post-dose, 75 min post-dose, 90 min post-dose, 105 min post-dose and 120 min post- dose.
|
Change from baseline BG level at minute 15,30,45,60,75,90,105, 120 post dose
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- DFGI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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