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Investigating the Effect of Whole-fruit Coffee Extract on Exercise Performance

Investigating the Effect of Whole-fruit Coffee Extract on Exercise Performance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05404841
Acronym
PACE
Enrollment
14
Registered
2022-06-03
Start date
2022-02-04
Completion date
2023-01-25
Last updated
2023-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caffine and Endurance Performance

Brief summary

Caffeine is a widely used efficacious supplement by both the general public, and athletes, with the goal of improving performance. The effects of caffeine alone are well known, but it is not clear whether a multi-ingredient supplement (containing both caffeine and polyphenols) can affect exercise performance. This study aims to determine if a low dose of caffeine, in the form of a whole-fruit coffee extract also containing polyphenols, can improve exercise performance compared to a placebo condition, with a secondary objective of identifying if this supplement can improve post exercise refuelling (glycogen resynthesis). Participants will consume either the supplement or a placebo before engaging in an exercise protocol. Muscle biopsies will then be obtained so as to measure subsequent glycogen resynthesis, with multiple blood samples being taken through the day. The following morning another biopsy will be taken before the exercise protocol will be repeated. This research will inform us of the efficacy of caffeine and polyphenols on improving exercise performance.

Interventions

DIETARY_SUPPLEMENTCoffeeBerry Supplement

A Coffeeberry supplement containing 200mg Caffeine and 14mg polyphenols, manufactured by FutureCeuticals Inc.,

DIETARY_SUPPLEMENTPlacebo

Placebo

Sponsors

VDF FutureCeuticals Inc.
CollaboratorINDUSTRY
University of Exeter
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Exclusion criteria

* Allergy to Lidocaine * Exclusion critera * Any diagnosed metabolic health condition * Pregnant * Non-habitual caffeine intake * Smoker * No endurance training * Diagnosed Cardiovascular disease * Beta-Blockers * Recent history of musculoskeletal injury Inclusion criteria: * Age 18-40 * Heathy * Highly trained endurance athletes (V̇O2max: males \>55 and females \>50 mL⋅kg bm-1⋅min-1) * Both males and females are allowed to participate. If females are on the oral contraceptive pill they are to be tested on consecutive weeks. If they are not on the oral contraceptive pill, then female subjects are to be tested every 4 weeks, at the same point of their menstrual cycle.

Design outcomes

Primary

MeasureTime frameDescription
Exercise performance15 MinituesAmount of work completed in 15 minutes

Secondary

MeasureTime frameDescription
Alertness1 Minitue10 cm visual analog scale (Ranging from Not Alert to Extremly Alert)
Motivation1 Minitue10 cm visual analog scale (Ranging from Not motivated to Extremly motivated)
Glycogen Resynthesis24 HoursThe diffrence in glycogen within the muscle between two time points
Urine osmolarity24 HoursThe hydration status of the individual measured in mOsmo\|/kg
GI comfort1 Minitue10 cm visual analog scale (Ranging from No discomfort to Extreme discomfort)
Rate of perceived exertion1 MinitueValidated Borg scale (6-20 Arbitrary units)

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026