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.
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
- Conditions the study is for
- Resistance Exercise Performance, Cognitive Function, Anaerobic Performance
- 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
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.
- Conditions
- Resistance Exercise Performance, Cognitive Function, Anaerobic Performance, Dietary Supplementation Athletic Performance
- 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 group | Role | What they receive |
|---|---|---|
| No-Capsule Control | No intervention | No supplement administered. Participants completed all testing procedures without receiving any substance. |
| Placebo | Placebo comparator | Participants received maltodextrin capsules matched in appearance to the blackcurrant supplement capsules. Receives: Dietary Supplement: Maltodextrin (Placebo) |
| Low-Dose Blackcurrant | Experimental | Participants received 250 mg of blackcurrant supplement per day. Receives: Dietary Supplement: Low-dose Blackcurrant Supplement |
| High-Dose Blackcurrant | Experimental | Participants 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.
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.
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)
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).
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)
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)
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)
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)
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.
- First posted2 Jun 2026
- Study start21 Jan 2023
- Primary completion25 Apr 2023
- Study completion10 Jul 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Resistance Exercise PerformanceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Jacksonville State University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Majid Koozehchian, PhD, Jacksonville State University
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.
Study at a glance
From the registry record, last updated by the sponsor on 2 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT07619976
- Acronym / sponsor ID
- NZBC-FORCE / JSU-EPNL-2026-02
- Conditions
- Resistance Exercise Performance, Cognitive Function, Anaerobic Performance, Dietary Supplementation Athletic Performance
- Keywords
- Blackcurrant, Anthocyanins, Anaerobic Exercise, Cognitive Function, Resistance Training, Dose-Response, Sports Nutrition, Placebo-Controlled
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Jacksonville State UniversityUniversity, hospital or other
- Study start
- 21 Jan 2023 (actual)
- Primary completion
- 25 Apr 2023 (actual)
- Study completion
- 10 Jul 2023 (actual)
- First posted
- 2 Jun 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
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.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Double blind (participant, investigator)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| No-Capsule Control | No intervention | –No supplement administered. Participants completed all testing procedures without receiving any substance. |
| Placebo | Placebo comparator | Dietary Supplement: Maltodextrin (Placebo)Participants received maltodextrin capsules matched in appearance to the blackcurrant supplement capsules. |
| Low-Dose Blackcurrant | Experimental | Dietary Supplement: Low-dose Blackcurrant SupplementParticipants received 250 mg of blackcurrant supplement per day. |
| High-Dose Blackcurrant | Experimental | Dietary Supplement: High-dose Blackcurrant SupplementParticipants received 600 mg of blackcurrant supplement per day. |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- 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
Key exclusion criteria (9 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Low-dose Blackcurrant SupplementA low-dose blackcurrant (250 mg) supplement was administered to examine its effects on anaerobic exercise performance and cognitive function. | Dietary supplement | Low-Dose Blackcurrant |
| High-dose Blackcurrant SupplementA high-dose blackcurrant (600 mg) supplement was administered to examine its effects on anaerobic exercise performance and cognitive function. | Dietary supplement | High-Dose Blackcurrant |
| Maltodextrin (Placebo)Maltodextrin capsules matched in appearance to the blackcurrant supplement capsules, serving as an inert placebo control. | Dietary supplement | Placebo |
Primary outcome
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.
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).
Anaerobic 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)
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).
6 secondary outcomes
Cognitive Function
Time frame: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation).
Rating of Perceived Exertion (RPE)
Time frame: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)
Heart Rate (HR)
Time frame: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)
Systolic Blood Pressure (SBP)
Time frame: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)
Diastolic Blood Pressure (DBP)
Time frame: Baseline, end of Week 1 (post-supplementation), end of Week 2 (post-washout), and end of Week 3 (post-crossover supplementation)
Tolerability and Adverse Events
Time frame: 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)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Jun 2026.
- Individual participant dataSharing planned: 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.
Related trials for Resistance Exercise Performance
Not yet recruiting
Acute Effects of Breathing Resistance During Exercise in Football Players
Respiratory Muscle Function and Football Performance
Recruiting
Effects of Rotator Cuff Drills Versus Progressive Resistance Exercises on Chronic Rotator Cuff Tendinopathy
Rotator Cuff Tendinosis
Recruiting
Acute Power Training Effects in Older Adults
Muscle Power, Functional Performance
Recruiting
Effect of Blood Flow Restriction on Recovery After Maximal Resistance Exercise
Recovery, Recovery Time
RecruitingObservational study
100-Year Human Aging Study
Aging, Aging Well
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.