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Resistance Exercise PerformanceNZBC-FORCENCT07619976

Effects of New Zealand Blackcurrant Supplementation on Exercise and Cognitive Performance in Resistance-Trained Adults

A study testing Low-dose Blackcurrant Supplement and High-dose Blackcurrant Supplement in people with Resistance Exercise Performance and Cognitive Function, run by Jacksonville State University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

New Zealand blackcurrant (NZBC) is a supplement made from a berry naturally rich in plant compounds called anthocyanins. Researchers have studied these compounds for years and found that they may help the body by improving blood flow, reducing post-exercise stress on the body, and supporting energy production. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
What is being tested?
Low-dose Blackcurrant Supplement and High-dose Blackcurrant Supplement
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
20 participants
Where
1 siteUnited States
Study dates
21 Jan 2023to 10 Jul 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age 18-40 years
  • At least 2 years of regular resistance training that included the bench press and either the leg press or squat
  • Body mass index (BMI) of 18.5-24.9 kg/m²

Who cannot join

  • Diagnosed with a metabolic, cardiovascular, or thyroid disorder
  • Current use of prescription or over-the-counter agents with potential cardiovascular or neurocognitive effects (e.g., beta-blockers or stimulants)
  • Tobacco use, vaping, or smokeless nicotine use
  • Self-reported blackcurrant sensitivity
  • Habitual alcohol intake greater than 12 standard drinks per week
  • Any recent musculoskeletal injury likely to impair testing
Show all 9Show fewer
  • Resting heart rate exceeding 100 bpm at familiarization
  • Resting blood pressure ≥140/90 mmHg at familiarization after repeat confirmation
  • Body fat percentage exceeding the study's predefined threshold at familiarization

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Exercise Physiology and Nutrition Laboratory (EPNL) at Jacksonville State University

    Jacksonville, Alabama, 36265-1724

Other trials in United States

About this study

Official title: Effects of Short-Term Low- and High-Dose New Zealand Blackcurrant Supplementation on Exercise and Cognitive Performance in Resistance-Trained Adults: A Randomized, Double-Blind, Placebo-Controlled Crossover Study

New Zealand blackcurrant (NZBC) is a supplement made from a berry naturally rich in plant compounds called anthocyanins. Researchers have studied these compounds for years and found that they may help the body by improving blood flow, reducing post-exercise stress on the body, and supporting energy production. Most of that research, however, has focused on endurance athletes like runners and cyclists. Almost nothing was known about whether NZBC could benefit people who do strength training. That is what this study was designed to find out.

Twenty healthy, resistance-trained men and women between the ages of 18 and 40 were recruited. Each participant completed four different conditions over the course of the study: taking no supplement at all, taking a placebo (a dummy capsule with no active ingredient), taking a low dose of NZBC (250 mg per day for seven days), and taking a higher dose of NZBC (600 mg per day for seven days). Neither the participants nor the researchers evaluating them knew which capsule was being taken at any given time, a design that helps ensure the results are as reliable as possible.

Read more

At the end of each seven-day period, participants came into the lab and completed a full battery of tests. Measurements included how much weight could be lifted for one maximum effort on the bench press and leg press, how much total volume could be completed across multiple sets, and how fast and powerfully the bar could be moved. Participants also completed a 30-second all-out cycling sprint to test anaerobic fitness, and a paper-and-pencil color-word test to measure focus and mental sharpness.

Strength increased noticeably. After taking either dose of NZBC, participants were able to lift more weight on both the bench press and leg press than when taking the placebo or no supplement. The lower dose had a particularly striking effect on leg training: participants pushed through roughly 38% more total volume in their leg press sets. For bar speed and explosive power on the bench press, the higher dose had the edge. Cognitive performance followed a similar pattern. The lower dose sharpened mental performance across several parts of the color-word test, while the higher dose made a more modest but still meaningful difference on one section. The sprint cycling test showed no differences between conditions. Importantly, both doses were safe and well-tolerated, with no meaningful side effects reported throughout the study.

One week of supplementation was sufficient to produce real differences in strength, power, and mental sharpness, and neither dose raised any safety concerns.

Read the detailed description

Background and Rationale Polyphenol-rich supplements have attracted growing interest in sports nutrition research, largely because of evidence that anthocyanins can influence several physiological processes relevant to exercise. These include improvements in vascular tone and blood flow, reductions in exercise-induced oxidative stress, changes in substrate utilization during activity, and improvements in fatigue tolerance. New Zealand blackcurrant (NZBC) extract has emerged as one of the more studied anthocyanin sources in this area, with prior research documenting benefits in high-intensity cycling, intermittent running, and fat oxidation during exercise.

Despite this growing body of evidence, nearly all existing research on NZBC has focused on endurance or aerobic exercise contexts. Whether NZBC could influence maximal strength, total lifting volume, or barbell power output in resistance-trained individuals had not been previously examined. Additionally, the potential for NZBC to influence cognitive function during resistance training is biologically plausible given its monoamine-related bioactive profile, but had not been rigorously tested in this population. This study was designed to address both gaps using a well-controlled crossover design.

Study Design This was a randomized, double-blind, placebo-controlled, four-period crossover trial conducted in the Exercise Physiology and Nutrition Laboratory at Jacksonville State University. The four conditions were a no-capsule control, a placebo, a low-dose blackcurrant condition (250 mg/day), and a high-dose blackcurrant condition (600 mg/day). Each capsule condition lasted seven consecutive days, with laboratory testing on day seven. The no-capsule control was always administered first; the three capsule conditions were assigned using a balanced 3×3 Williams design to minimize carryover effects. Randomization was computer-generated by an investigator independent of data collection. All capsule conditions were separated by washout periods, and capsules were identical in appearance and mass to maintain blinding.

Interventions The placebo capsule contained 600 mg of maltodextrin per day. The low-dose condition contained 250 mg of NZBC extract plus 350 mg of maltodextrin per day, providing an estimated 87.5 mg of anthocyanins daily. The high-dose condition delivered 600 mg of NZBC extract per day, providing approximately 210 mg of anthocyanins daily. Capsules were taken once daily, timed two hours before training on workout days or at noon on rest days. On laboratory testing days, the final capsule was taken on-site two hours before testing, with staff present to confirm ingestion.

Dietary standardization was implemented throughout the study. Beginning two weeks before the first test session, participants discontinued all dietary supplements and over-the-counter medications. In the 72 hours preceding each laboratory visit, participants abstained from structured exercise, caffeine, alcohol, dietary nitrate, polyphenol-rich foods, and antibacterial mouthwash. Dietary intake was monitored using four separate three-day recording windows via MyFitnessPal to verify consistency across conditions.

Statistical Analysis Each outcome was analyzed using a repeated-measures general linear model with treatment (four levels) as the within-subject factor and sex as the between-subject factor. The model tested the main effect of treatment and the treatment-by-sex interaction. Sphericity was assessed using Mauchly's test, with Greenhouse-Geisser corrections applied where needed. Significant overall treatment effects were followed by pairwise comparisons using estimated marginal means with the least significant difference procedure. Effect sizes for pairwise comparisons were calculated as Cohen's d_z and interpreted as trivial, small, moderate, or large. All analyses were conducted in IBM SPSS Statistics, version 31.

Being tested
Low-dose Blackcurrant Supplement, High-dose Blackcurrant Supplement, Maltodextrin (Placebo)
Keywords
Blackcurrant, Anthocyanins, Anaerobic Exercise, Cognitive Function, Resistance Training, Dose-Response, Sports Nutrition, Placebo-Controlled

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Low-dose Blackcurrant SupplementDietary supplement

    A low-dose blackcurrant (250 mg) supplement was administered to examine its effects on anaerobic exercise performance and cognitive function.

  • High-dose Blackcurrant SupplementDietary supplement

    A high-dose blackcurrant (600 mg) supplement was administered to examine its effects on anaerobic exercise performance and cognitive function.

  • Maltodextrin (Placebo)Dietary supplement

    Maltodextrin capsules matched in appearance to the blackcurrant supplement capsules, serving as an inert placebo control.

Study groups in NCT07619976
Study groupRoleWhat they receive
No-Capsule ControlNo interventionNo supplement administered. Participants completed all testing procedures without receiving any substance.
PlaceboPlacebo comparatorParticipants received maltodextrin capsules matched in appearance to the blackcurrant supplement capsules.
Receives: Dietary Supplement: Maltodextrin (Placebo)
Low-Dose BlackcurrantExperimentalParticipants received 250 mg of blackcurrant supplement per day.
Receives: Dietary Supplement: Low-dose Blackcurrant Supplement
High-Dose BlackcurrantExperimentalParticipants received 600 mg of blackcurrant supplement per day.
Receives: Dietary Supplement: High-dose Blackcurrant Supplement

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Resistance Exercise Performance

    Bench press and leg press 1RM, total lifting volume (sets × reps × weight), and Tendo-derived peak and mean barbell power during bench press. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout). Each measure reported separately in its respective unit (kg for 1RM and volume; watts for power).

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation); total study duration approximately 3 weeks.

  2. Anaerobic Exercise Performance

    Peak power, mean power, and total work were measured via the 30-second Wingate Anaerobic Test. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout). Each measure reported separately in its respective unit (watts for peak and mean power; joules for total work).

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)

Secondary outcomes (6)
  1. Cognitive Function

    Cognitive performance assessed using the Stroop Color-Word Test, measuring selective attention, cognitive flexibility, and processing speed. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout).

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation).

  2. Rating of Perceived Exertion (RPE)

    Perceived exertion was recorded using the Borg 6-20 scale at 1 minute post-bench press and post-leg press. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout).

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)

  3. Heart Rate (HR)

    Resting and post-exercise heart rate recorded at rest and 1 minute after the bench press, leg press, and Wingate test. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout).

    Unit of Measure: beats per minute (bpm)

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)

  4. Systolic Blood Pressure (SBP)

    Resting and post-exercise systolic blood pressure recorded at rest and 1 minute after the bench press, leg press, and Wingate test. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout).

    Unit of Measure: mmHg

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)

  5. Diastolic Blood Pressure (DBP)

    Resting and post-exercise diastolic blood pressure recorded at rest and 1 minute after the bench press, leg press, and Wingate test. Assessed at 4 time points across a crossover design (1-week supplementation, 1-week washout).

    Unit of Measure: mmHg

    Measured: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)

  6. Tolerability and Adverse Events

    Side-effects questionnaire assessing physical and psychological symptoms during each capsule condition (Placebo, Low-Dose Blackcurrant, and High-Dose Blackcurrant).

    Measured: During each of 3 supplementation weeks: Week 1, Week 2, and Week 3 (PL, LDBC, and HDBC conditions, each 1 week with 1-week washout between conditions)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Jun 2026
  2. Study start21 Jan 2023
  3. Primary completion25 Apr 2023
  4. Study completion10 Jul 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07619976
Sponsor's protocol ID
JSU-EPNL-2026-02
Other IDs
IRB #12132022-01
Acronym
NZBC-FORCE
Status last verified
May 2026
First submitted
17 May 2026
Last updated
2 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Deidentified individual participant data (IPD) for all primary and secondary outcome measures, including resistance exercise performance, anaerobic exercise performance, cognitive function (Stroop Color-Word Test), hemodynamic responses, rating of perceived exertion, and adverse events, will be made available upon reasonable request to the corresponding author beginning 6 months after publication.

Questions about this trial

What is this clinical trial studying?

A study testing Low-dose Blackcurrant Supplement and High-dose Blackcurrant Supplement in people with Resistance Exercise Performance and Cognitive Function, run by Jacksonville State University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Resistance Exercise Performance (time frame: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation); total study duration approximately 3 weeks.). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jun 2026.

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