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Dietary SupplementsCAF+BJNCT06596395

Effect of Acute Caffeine and Beetroot Juice Intake on Strength, Power, and Muscular Endurance

A study testing Acute caffeine and beetroot juice, Acute caffeine and Acute beetroot juice in people with Dietary Supplements and Caffeine, run by University of Alcala at 1 site in Spain.

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

Introduction: Several studies have evaluated and confirmed the ergogenic effect of acute caffeine and beetroot juice intake on sports performance. However, there are few studies focused on the production of strength, power, and muscle endurance, particularly when both supplements are ingested together. Read more about this study

Who is it for?
Ages 18 to 35 years, men onlyHealthy volunteers can take part
Conditions the study is for
Dietary Supplements, Caffeine, Nitrates
What is being tested?
Acute caffeine and beetroot juice, Acute caffeine and Acute beetroot juice
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
14 participants
Where
1 siteSpain
Study dates
1 Sep 2023to 1 May 2024
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 35 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age between ≥ 18 and ≤ 35 years.
  • Body Mass Index (BMI) \< 25 kg/m².
  • Resistance-trained individuals (\> 2 years of structured trained).
  • Healthy men and women without neurological, cardiometabolic, immunological, or physical conditions that prevent them from exercising.
  • Participants must be able to perform the tests described in the following section.

Who cannot join

  • History of neuromuscular diseases, heart diseases, or diseases that may affect liver or muscle metabolism.
  • Use of drugs, other stimulants or sport supplements that interfere with the intake of the study\'s dietary supplements.
  • Sedentary habits (\< 150 min/week of moderate exercise).
  • Having undergone prolonged periods of forced physical inactivity during the 6 months prior to the study.
  • Performing strenuous exercise during the 48 hours prior to the tests.
  • Failure to replicate the same food intake on the two days of the experiments.
  • Consuming caffeine or any other stimulant after 6 pm the day before the training or tests, to avoid headaches, discomfort, or lethargy among regular caffeine consumers.
  • Consuming foods rich in NO3- (e.g., beetroot, spinach, or celery) during the 48 hours prior to each experimental condition.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Facultad de Medicina y Ciencias de la Salud. Universidad de Alcalá

    Alcalá de Henares, Madrid, 28805

Other trials in Spain

About this study

Official title: Effect of Acute Caffeine and Beetroot Juice Intake on Strength, Power, and Muscular Endurance Based on Circadian Rhythms.

Introduction: Several studies have evaluated and confirmed the ergogenic effect of acute caffeine and beetroot juice intake on sports performance. However, there are few studies focused on the production of strength, power, and muscle endurance, particularly when both supplements are ingested together.

Objectives: Evaluate the acute effect of combined and isolated intake of caffeine and beetroot juice on the production of strength, power, and muscle endurance in young adults, analyzing the effect of circadian rhythms (morning vs. afternoon) on the exercise performed (bench press vs. squat).

Methods: A total of 12 healthy and physically active participants will be recruited for the study. Through a double-blind, crossover, randomized, and controlled design, participants will ingest: a) Caffeine (3 mg/kg body mass); b) Beetroot juice (70 ml, 6.5 mmol of nitrates); c) Caffeine + Beetroot juice; d) Placebo (maltodextrin, 3 mg/kg). The supplements will be ingested 120 minutes (beetroot juice or placebo) and 60 minutes before (caffeine or placebo), the latter dissolved in 200 ml of water. After the ingestion period, strength, power, and muscle endurance will be analyzed with 1RM tests, strength and power tests at 25%, 50%, 75%, and 90% 1RM, and muscle endurance tests at 65% 1RM, in all cases for squat and bench press exercises. Additionally, dynamometry (manual and the isometric mid-thigh pull test) and vertical jump (squat jump and countermovement jump) will be analyzed. The four experimental conditions will be conducted in the morning (8:00 am to 10:00 am) and in the afternoon (4:30 pm to 6:30 pm).

Being tested
Acute caffeine and beetroot juice, Acute caffeine, Acute beetroot juice, Placebo

What participants receive

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

  • Acute caffeine and beetroot juiceDietary supplement

    Combined effect of beetroot juice and caffeine intake on muscular strength, power and endurance performance

  • Acute caffeineDietary supplement

    single effect of caffeine intake on muscular strength, power and endurance performance

  • Acute beetroot juiceDietary supplement

    single effect of beetroot juice intake on muscular strength, power and endurance performance

  • PlaceboDietary supplement

    single effect of placebo on muscular strength, power and endurance performance

Study groups in NCT06596395
Study groupRoleWhat they receive
Caffeine + Beetroot JuiceExperimental70 mL of concentrated NO3--rich (BJ, 6.5 mmol NO3-) + 3 mg/kg of caffeine
Receives: Dietary Supplement: Acute caffeine and beetroot juice
Beetroot JuiceExperimental70 mL of concentrated NO3--rich (BJ, 6.5 mmol NO3-) + 3 mg/kg of placebo (maltodextrin)
Receives: Dietary Supplement: Acute beetroot juice
CaffeineExperimental70 mL of NO3--depleted (BJ, 0.04 mmol NO3-) + 3 mg/kg of caffeine
Receives: Dietary Supplement: Acute caffeine
PlaceboPlacebo comparator70 mL of NO3--depleted (BJ, 0.04 mmol NO3-) + 3 mg/kg of placebo (maltodextrin)
Receives: Dietary Supplement: Placebo

What is being measured

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

  1. Mean and peak velocity and time to reach peak velocity at different %1RM

    Measuring bar velocity desplacement during bench press and back squat exercises.

    Measured: On each trial, after dietary supplement intake, during 2 weeks

  2. Mean and peak power output and time to reach peak power output at different %1RM

    Measuring power output generated during bench press and back squat exercises.

    Measured: On each trial, after dietary supplement intake, during 2 weeks

  3. Number of repetitions performed at 65%1RM until task failure

    Additionally to mean and peak velocity, mean and peak power output, time to reach peak velocity and peak power

    Measured: On each trial, after dietary supplement intake, during 2 weeks

Secondary outcomes (4)
  1. Mood state (tension, depression, anger, vigor, fatigue and confusion)

    Participants graded a set of 29 items related to the mood on a Likert scale from 0 (not at all) to 4 (extremely) in reply to the question \"How do you feel at this moment?\" to assess six scales: tension, depression, anger, vigor, fatigue and confusion.

    Measured: On each trial, after dietary supplement intake, during 2 weeks

  2. Adverse effects

    perception of power, endurance, energy and exertion, as well as heart, muscular and gastrointestinal discomfort.

    Measured: On each trial, after dietary supplement intake, during 2 weeks

  3. handgrip and isometric mid-thigh pull tests

    N generated

    Measured: On each trial, after dietary supplement intake, during 2 weeks

  4. Vertical Jump (cm and power)

    Measured: On each trial, after dietary supplement intake, during 2 weeks

Timeline

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

  1. First posted19 Sep 2024
  2. Study start1 Sep 2023
  3. Primary completion30 Jan 2024
  4. Study completion1 May 2024

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
Other
Allocation
Randomised
Intervention model
Crossover
Model description
Triple-blind, cross-over, randomized controlled-trial
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
14 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06596395
Sponsor's protocol ID
CEIP/2023/4/093
Acronym
CAF+BJ
Status last verified
Sep 2024
First submitted
6 Sep 2024
Last updated
19 Sep 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

A study testing Acute caffeine and beetroot juice, Acute caffeine and Acute beetroot juice in people with Dietary Supplements and Caffeine, run by University of Alcala at 1 site in Spain.

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 5 inclusion and 8 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 19 Sep 2024. 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 Spain. 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?

Mean and peak velocity and time to reach peak velocity at different %1RM (time frame: On each trial, after dietary supplement intake, during 2 weeks). The study lists 3 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 19 Sep 2024.

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