- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07729631
Establishing the Glycaemic Index of Vegetable Smoothies (VEG-GI)
July 22, 2026 updated by: Emma Greatorex Brooks, University of Bath
Study to Establish Glycaemic Response to the Ingestion of Vegetable Smoothies Expressed as Glycaemic Index Following Best Practice Guidelines
Glycaemic responses to carbohydrates ingested as fruit and vegetables may vary depending on factors inherent to the fruit or vegetable, and on the type of sugar.
The aim of this project is to investigate the glycaemic responses to two new fruit and vegetable smoothies, and to establish the glycaemic index for each product relative to a glucose reference.
Participants will undertake 4 postprandial tests with 2 different test drinks following best practice guidelines for glycaemic index testing.
The test drinks (GREEN and RED) will be matched for carbohydrate to the glucose reference (CONTROL) which will be sampled two times.
Fingerstick capillary blood sampling will measure glucose concentrations.
These data will provide insight into how differing formulations can alter the glycaemic responses to fruit and vegetable drinks.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
16
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bath, United Kingdom, BA2 7AY
- Department for Health, University of Bath
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age: 18-65 years
- Body mass index 18-30 kg/m2
Exclusion Criteria:
- diagnosis of any form of diabetes
- intolerances or allergies to any of the study procedures (e.g. fructose/inulin intolerance)
- Fructose malabsorption
- Inborn errors of fructose metabolism (e.g. fructokinase deficiency, aldolase B deficiency, fructose-1,6-bisphosphatase deficiency)
- pregnant or lactating
- any condition that could introduce bias to the study (e.g. diagnoses of lipid disorders, including cardiovascular disease, or therapies that alter lipid or glucose metabolism, such as statins or niacin).
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: CONTROL
50 g glucose (55 g dextrose powder accounting for hydration) plus 519 mL water
|
Commercially available fruit and vegetable smoothie
|
|
Active Comparator: REPLICATE CONTROL
50 g glucose (55 g dextrose powder accounting for hydration) plus 519 mL water
|
Commercially available fruit and vegetable smoothie
|
|
Experimental: RED
500 mL of commercially available "Red Goodness" providing 50 g of carbohydrate [apple (47%), banana, chayote (8%), beetroot (7%), carrot (5%), cucumber (5%), cherry (3%), spinach (2%), mandarin, lemon, apple water, beetroot extract].
Plus 19 mL water to standardise volume
|
Commercially available fruit and vegetable smoothie
|
|
Experimental: GREEN
519 mL of commercially available "Green Goodness" smoothie providing 50 g carbohydrate [apples (46%), banana, courgette (10%), chayote (8%), guava, cucumber (5%), lemon (3%), spinach (2%), mandarin, apple water spirulina extract, turmeric extract, mint extract].
|
Commercially available fruit and vegetable smoothie
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Glycaemic indices for 2 test drinks measured using capillary blood samples
Time Frame: 120 minutes
|
Glycaemic indices [2-hour incremental area under the glucose curve (mmol/L-1x120 minutes) for each of the 2 test drinks relative to mean value of control conditions (CONTROL, REPLICATE CONTROL), expressed as a percentage] in capillary blood samples
|
120 minutes
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparisons between conditions in glucose concentration in capillary samples
Time Frame: 120 minutes
|
Comparison of blood glucose concentration 2-hour incremental area under the curve (iAUC) min.mmol/L
between test conditions
|
120 minutes
|
|
Comparisons between conditions in glucose concentration in capillary samples
Time Frame: 120 minutes
|
Comparison of postprandial peak concentration mmol/L of blood glucose between test conditions (Cmax)
|
120 minutes
|
|
Comparisons between conditions in glucose concentration in capillary samples
Time Frame: 120 minutes
|
Comparison of time to peak blood glucose concentration in minutes (Tmax) between test conditions
|
120 minutes
|
|
Comparisons between conditions in glucose concentration in capillary samples
Time Frame: 120 minutes
|
Comparison of blood glucose concentration mmol/L at 2 hours between test conditions
|
120 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Brouns F, Bjorck I, Frayn KN, Gibbs AL, Lang V, Slama G, Wolever TM. Glycaemic index methodology. Nutr Res Rev. 2005 Jun;18(1):145-71. doi: 10.1079/NRR2005100.
- Gonzalez JT. Are all sugars equal? Role of the food source in physiological responses to sugars with an emphasis on fruit and fruit juice. Eur J Nutr. 2024 Aug;63(5):1435-1451. doi: 10.1007/s00394-024-03365-3. Epub 2024 Mar 16.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 22, 2025
Primary Completion (Actual)
December 15, 2025
Study Completion (Actual)
December 15, 2025
Study Registration Dates
First Submitted
July 22, 2026
First Submitted That Met QC Criteria
July 22, 2026
First Posted (Actual)
July 27, 2026
Study Record Updates
Last Update Posted (Actual)
July 27, 2026
Last Update Submitted That Met QC Criteria
July 22, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 10814-13276
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
De-identified data will be made available open access on the University of Bath Research Data Archive (RDA) at the point of publication in a peer-reviewed journal
IPD Sharing Time Frame
These will become available at the point of publication permanently
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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