New treatment option for Effect of Resveratrol on Performance and Recovery
Official title Effect of Resveratrol Supplementation on Exercise Performance and Recovery
ClinicalTrials.gov ID: NCT06723119
What this study is testing
- What it's testing
- 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).
- You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 40, men only. Healthy volunteers may be eligible.
You may be able to join if
- 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...
- Participants must be willing to abstain from the consumption of bananas of non-steroidal anti-inflammatory drugs (NSAIDs) for the duration of their...
You likely can't join if
- 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...
- 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...
See the full eligibility 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...
- 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
- 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...
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Orlando, Florida, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling male, 18 years to 40 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Orlando, Florida, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.