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Tart Cherry Extract for Muscle Recovery (TCR Trial)

N/A
Waitlist Available
Led By Chad M Kerksick, PhD
Research Sponsored by Lindenwood University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 10 days
Awards & highlights

TCR Trial Summary

This trial evaluates effects of tart cherry powder on muscle power & force, soreness, inflammation & oxidative stress after sprints in male & female athletes.

Who is the study for?
This trial is for healthy men and women aged 18-35 who exercise at least four days a week, including high-intensity workouts. Participants should have a BMI of 18.0 - 30.0 kg/m2, though certain exceptions apply based on body fat percentage. They must not have any major health issues or be taking medications that affect muscle recovery.Check my eligibility
What is being tested?
The study tests if powdered tart cherry extract helps with muscle recovery after intense sprints compared to a placebo. It measures changes in muscle strength, soreness, inflammation, and oxidative stress in trained individuals following the sprinting activity.See study design
What are the potential side effects?
While the side effects are not explicitly listed for this trial, powdered tart cherry is generally considered safe with potential mild digestive discomfort as a common concern when consumed in large quantities.

TCR Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~10 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 10 days for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Changes in Creatine Kinase concentrations
Changes in Creatine Kinase-myocardial band concentrations
Counter movement Jump Height
+8 more
Secondary outcome measures
Changes in 8-isoprostane concentration
Changes in IL-10 concentration
Changes in IL-6 concentration
+7 more
Other outcome measures
Reported Adverse Events
Resting Blood pressure
Resting Heart Rate

TCR Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Tart Cherry Extract PowderExperimental Treatment1 Intervention
Tart Cherry Extract Powder (NordicCherry, SpecNova, LLC). Dispensed during visit 1. Participants will consume 1 dose per day for 10 days.
Group II: PlaceboPlacebo Group1 Intervention
Rice Flour. Dispensed during visit 1. Participants will consume 1 dose per day for 10 days.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tart Cherry Extract Powder
2023
N/A
~40

Find a Location

Who is running the clinical trial?

Lindenwood UniversityLead Sponsor
18 Previous Clinical Trials
726 Total Patients Enrolled
Chad M Kerksick, PhDPrincipal InvestigatorLindenwood University
7 Previous Clinical Trials
328 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Does this investigation accept participants who are at least 45 years old?

"This medical trial is recruiting participants who are of legal age and younger than 35 years old."

Answered by AI

Are there still openings available for participants in this clinical investigation?

"According to clinicaltrials.gov, this experiment is open for recruitment and was first announced on April 25th of 2023 with the latest edits having been made on November 2nd of that same year."

Answered by AI

How many participants will be included in this medical experiment?

"Affirmative. The information available on clinicaltrials.gov demonstrates that this medical trial, originally published on April 25th 2023, is currently recruiting participants. 40 patients are required for the study to be conducted at one particular site."

Answered by AI

Could I be accepted to participate in this experiment?

"To be eligible to join this clinical trial, individuals must suffer from muscular pain and fall in the age bracket of 18-35 years old. A total of 40 patients are required for enrolment."

Answered by AI

What are the main goals of this experimental research study?

"This 10 day experiment is designed to measure Counter movement Jump Height, with secondary objectives being Peak Power during a Wingate Anaerobic Test, Desire to Exercise Visual Analog Scale (range of 0-100), and Pittsburgh Sleepiness Scale Score (lower scores equate higher sleepiness)."

Answered by AI
~20 spots leftby May 2025