Orlando, FLNCT06723119Now EnrollingIRB Ready

Effect of Resveratrol on Performance and Recovery Clinical Trial in Orlando, FL

Access cutting-edge effect of resveratrol on performance and recovery treatment through this clinical trial at a research site in Orlando. Study-provided care at no cost to qualified participants.

Sponsored by University of Central Florida

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IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related effect of resveratrol on performance and recovery treatment provided free

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Why Participate?

  • No-Cost Study Care

  • Local to Orlando

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Orlando site if eligible
  4. 4Begin participation

About This Effect of Resveratrol on Performance and Recovery Study in Orlando

To examine the effects of once daily supplementation with 500mg VeriSperse® resveratrol (VRES) for 17 days on muscle function, delayed onset muscle soreness, systemic concentrations of muscular damage markers and markers of oxidative stress in resistance trained young adult males following a damaging isoinertial squat protocol (ISP).

Sponsor: University of Central Florida

Who Can Participate

Inclusion Criteria

• Male between the ages of 18-40 years old
Healthy, and ready for physical activity as determined by the PAR-Q+, and MHQ.
Participants will be required to be recreationally active (defined according to ACSM standards of at least 150 minutes exercise per week).
Participants will be required to have been actively resistance training for a minimum of 6 months as defined by 3 resistance training sessions per week with at least one lower body session.
Participants must be willing to abstain from the consumption of bananas of non-steroidal anti-inflammatory drugs (NSAIDs) for the duration of their enrollment in study.
Participants must be willing to abstain from dietary supplementation that are viewed by study investigators to confound the outcomes of the study (e.g., Creatine). Those currently supplementing must be willing to undergo a 28-day washout prior to beginning study procedures.
Participants must be consuming \<300 mg·day-1 (Equivalent to 3 cups of coffee per day or 2 16oz cans of Redbull) and willing to keep their caffeine consumption consistent throughout the duration of the study.
Participants will be required to have access to the online MyFitnessPal application either via cellphone or computer and be willing to download and maintain the application for the duration of the study.
Free from previous or current lower body injuries that are viewed by the investigators to potentially limit ability of the participant to perform the assessments.
Willing to abstain from lower body resistance training for the 14 days preceding ET1 and ET2

Exclusion Criteria

• Individual does not provide consent to participate in this study.
Inability to perform physical exercise (determined by MHQ, and PAR Q+). That is Answering "Yes" to any question on the PAR-Q +, or having a pre-existing condition such as musculoskeletal injury, back pain, chronic pain etc. that the investigative team perceives will prevent a participant from safely completing the protocol.
Not currently participating in at least 150 minutes of physical activity per week.
Not currently resistance trained (as defined within the inclusion criteria)
Currently taking any performance-enhancing drug (determined from health and activity questionnaire)
Currently taking a nutritional supplement known to improve physical performance and not willing refrain form the consumption of the supplement for at least 28-days prior to beginning study procedures.
Regularly taking any type of prescription or over-the-counter medication deemed to affect performance, or having any chronic illnesses, which require medical care.
Have used nicotine or tobacco at any time within the last three months.
Report consuming bananas or NSAIDS at any time during your enrollment in the study.
Report daily caffeine consumption \>300 mg·day-1
Report any lower extremity muscle soreness for visits ET1 and ET2
Previous or current lower body injuries viewed by the investigators to potentially limit the ability of the participant to perform the assessments.
Inability or unwillingness to consume the provided standardized snacks and meals in their entirety.
Inability or unwillingness to adhere to the diet restrictions of the study.
Have a food allergy to either of the two provided energy bars.
Inability or unwillingness to report all food and beverage consumption during the two 5-day dietary log periods.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Orlando?

Yes, this clinical trial (NCT06723119) has an active research site in Orlando, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Effect of Resveratrol on Performance and Recovery Treatment Options in Orlando, FL

If you're searching for effect of resveratrol on performance and recovery treatment options in Orlando, FL, this clinical trial (NCT06723119) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Orlando research site is actively enrolling participants for this clinical trial. You'll receive care from experienced effect of resveratrol on performance and recovery specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all effect of resveratrol on performance and recovery clinical trials near you to find additional studies recruiting in your area.

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