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Upprätta det glykemiska indexet för fruktdrycker med olika mätmetoder

17 september 2026 uppdaterad av: Emma Greatorex Brooks, University of Bath

Studie för att undersöka glykemiska svar på intag av fruktjuicer och smoothies med olika mätmetoder.

Glycaemic responses to carbohydrates ingested as fruit sugars may vary depending on factors inherent to the fruit and the type of sugar. The aim of this project is to investigate the glycaemic responses to a range of commercially available fruit drinks and to establish the glycaemic index for each product relative to a glucose reference. Differences in recorded responses could also be influenced by the sample type (capillary blood vs interstitial fluid) and participant characteristics. Participants will ingest 8 test drinks including 5 different fruit drinks (OJ, AJ, S&B, ENERGISE, BLUE), each matched for carbohydrate to the glucose reference (CONTROL) which will be sampled two times, an additional sample of one of the smoothies (S&B) will also be replicated. Fingerstick capillary blood sampling alongside dual sited continuous glucose monitors (CGM) will measure glucose and lactate concentrations, subjective appetite sensations will also be recorded. The tests will follow best practice guidelines for glycaemic index testing. These data will provide insight into how differing formulations can alter the glycaemic responses to fruit drinks, and whether sampling technique can affect the interpretations of measurement.

Studieöversikt

Status

Avslutad

Intervention / Behandling

Studietyp

Interventionell

Inskrivning (Faktisk)

11

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Bath, Storbritannien, BA2 7AY
        • Department for Health, University of Bath

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 65 år (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Allt

Beskrivning

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).

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Grundläggande vetenskap
  • Tilldelning: Randomiserad
  • Interventionsmodell: Crossover tilldelning
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: CONTROL

50 g glucose (55 g dextrose powder accounting for hydration) plus 641 mL water

Commercially available fruit drinks or smoothies

Aktiv komparator: REPLICATE CONTROL

50 g glucose (55 g dextrose powder accounting for hydration) plus 641 mL water

Commercially available fruit drinks or smoothies

Experimentell: S&B

417 mL of commercially available "Strawberries & Bananas" fruit smoothie providing 50 g carbohydrate [strawberries (31%), apples, bananas (22%), white grapes, oranges, blackcurrants]. Plus 224 mL water to standardise volume

Commercially available fruit drinks or smoothies

Experimentell: REPLICATE S&B

417 mL of commercially available "Strawberries & Bananas" fruit smoothie providing 50 g carbohydrate [strawberries (31%), apples, bananas (22%), white grapes, oranges, blackcurrants]. Plus 224 mL water to standardise volume

Commercially available fruit drinks or smoothies

Experimentell: OJ

641 mL of commercially available "Smooth Orange Juice" providing 50 g of carbohydrate [100% oranges]

Commercially available fruit drinks or smoothies

Experimentell: AJ

455 mL commercially available "Apple Juice" providing 50 g of carbohydrate [apples, ascorbic acid]. Plus 186 mL water to standardise volume

Commercially available fruit drinks or smoothies

Experimentell: ENERGISE

417 mL of commercially available "Energise Super Smoothie" providing 50 g carbohydrate [apples (50%), red grapes, bananas, strawberries (10%), blackcurrants, sour cherries (3.3%), pressed beetroot, flax seeds (0.56%), guarana infusion (0.01%), vitamins B1, B2, B3, B6, C & E]. Plus 224 mL water to standardise volume

Commercially available fruit drinks or smoothies

Experimentell: BLUE

521 mL of commercially available "Bolt from the Blue" juice drink providing 50 g carbohydrate [apple (66%), coconut water (18%), white grapes, white guava (5.2%), passion fruit, lime (0.87%), spirulina extract (0.81%) vitamins B1, B2, B3, B6, C & E]. Plus 120 mL water to standardise volume

Commercially available fruit drinks or smoothies

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Glycaemic indices for 5 test drinks measured using capillary blood samples
Tidsram: 120 minutes

Glycaemic indices [2-hour incremental area under the glucose curve (mmol/L-1x120 minutes) for each of the 5 test drinks relative to mean value of control conditions (CONTROL, REPLICATE CONTROL), expressed as a percentage] in capillary blood samples

120 minutes

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Glycaemic index of all conditions with capillary blood samples vs CGM
Tidsram: 120 minutes

The difference in glycaemic index [2-hour incremental area under the glucose curve (mmol/L-1x120 minutes) for 5 test drinks relative to mean control (CONTROL, REPLICATE CONTROL), expressed as a percentage] in capillary blood samples versus continuous glucose monitors.

120 minutes

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Comparisons between conditions in glucose concentration in capillary samples
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 120 minutes

Comparison of blood glucose concentration mmol/L at 2 hours between test conditions

120 minutes
Comparisons between conditions in glucose concentration with CGM
Tidsram: 120 minutes

Comparison of glucose concentration 2-hour incremental area under the curve (iAUC) min.mmol/L between test conditions

120 minutes
Comparisons between conditions in glucose concentration with CGM
Tidsram: 120 minutes

Comparison of postprandial peak concentration mmol/L of glucose between test conditions (Cmax)

120 minutes
Comparisons between conditions in glucose concentration with CGM
Tidsram: 120 minutes

Comparison of time to peak glucose concentration in minutes (Tmax) between test conditions

120 minutes
Comparisons between conditions in glucose concentration with CGM
Tidsram: 120 minutes

Comparison of glucose concentration mmol/L at 2 hours between test conditions

120 minutes
Comparisons between conditions in lactate concentration in capillary samples
Tidsram: 120 minutes

Comparison of blood lactate concentration 2-hour incremental area under the curve (iAUC) min.mmol/L between test conditions

120 minutes
Comparisons between conditions in lactate concentration in capillary samples
Tidsram: 120 minutes

Comparison of postprandial peak concentration mmol/L of blood lactate between test conditions (Cmax)

120 minutes
Comparisons between conditions in lactate concentration in capillary samples
Tidsram: 120 minutes

Comparison of time to peak blood lactate concentration in minutes (Tmax) between test conditions

120 minutes
Comparisons between conditions in lactate concentration in capillary samples
Tidsram: 120 minutes

Comparison of blood lactate concentration mmol/L at 2 hours between test conditions

120 minutes
Comparisons between conditions of appetite ratings
Tidsram: 120 minutes

Comparison of subjective appetite sensations assessed with visual analogue scales (2-hour area under the curve min.mmVAS)

120 minutes
Comparisons between individuals
Tidsram: 120 minutes

Comparison of Postprandial lactate concentration min.mmol/L between individuals 2-hour incremental area under curve (iAUC)

120 minutes
Comparisons between individuals
Tidsram: 120 minutes

Comparison of Postprandial glucose concentration min.mmol/L between individuals 2-hour incremental area under curve (iAUC)

120 minutes
Comparisons between individuals
Tidsram: 120 minutes

Comparison of Appetite rating responses min.mmVAS between individuals 2-hour area under curve (AUC)

120 minutes
Comparisons within individuals
Tidsram: 120 minutes

Comparison within individuals of interstitial glucose concentrations measurements from continuous glucose monitors on left and right arms.

120 minutes

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

13 mars 2025

Primärt slutförande (Faktisk)

9 juli 2025

Avslutad studie (Faktisk)

9 juli 2025

Studieregistreringsdatum

Först inskickad

28 februari 2025

Först inskickad som uppfyllde QC-kriterierna

20 mars 2025

Första postat (Faktisk)

27 mars 2025

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

22 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

17 september 2026

Senast verifierad

1 september 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 7134-9931

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

JA

IPD-planbeskrivning

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.

Tidsram för IPD-delning

These will become available at the point of publication permanently

IPD-delning som stöder informationstyp

  • STUDY_PROTOCOL
  • SAV
  • ICF

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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