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Impact of 60 Days Powdered Tart Cherry Supplementation on Metabolic Syndrome

Not Applicable
Recruiting
Conditions
Metabolic Syndrome
Interventions
Dietary Supplement: Placebo
Dietary Supplement: Powdered tart cherry
Registration Number
NCT05614947
Lead Sponsor
Ohio University
Brief Summary

Metabolic syndrome (MetSyn) is a growing health concern, with up to 25% of the worlds population having the syndrome. MetSyn is a primary risk factor for cardiovascular disease and type II diabetes development, and is independently associated with all-cause mortality, making it an important disease target. The primary treatment for MetSyn is exercise and weight loss, along with medically necessary treatment. Exercise, along with dietary changes such as increased fiber and polyphenol intake can positively impact many of the metabolic abnormalities seen with MetSyn. For example, polyphenols have been shown to decrease lipid concentration and improved glucose clearance as well as decreased oxidative stress and inflammation. Powdered tart cherry capsules, which contain the skin of the fruit, provides polysaccharides (fiber) that would likely act as a substrate for gut bacteria degradation, providing energy substrates and barrier integrity to the colonocytes and increasing the bioavailability of the polyphenols to other cells in the body. However there have been no long-term investigations into the use of powdered tart cherry supplements in MetSyn, therefore we aim to determine if 60 days tart cherry supplementation modify criteria for MetSyn in currently diagnosed individuals including body mass, waist circumference, blood pressure, blood lipid levels and blood glucose control.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Have been diagnosed with metabolic syndrome by a physician or meet the diagnostic criteria: Waist circumference greater than 40 inches (men) or greater than 35 inches (women), High blood pressure (greater than 130/80) or taking medication for high blood pressure, High triglycerides (greater than 150 mg/dL) or low HDL (less than 40 for men, less than 50 for women), High fasting blood glucose (100-126 mg/dL) or diagnosed as pre-diabetic
  • Age 25-60
Exclusion Criteria
  • currently taking medication for glucose or lipid control, such as metformin and/or statin
  • currently using anti-inflammatory medications & have not used corticosteroids in the last two months
  • diagnosed with or currently being treated for an inflammatory condition
  • major organ system impairment (heart failure, renal failure, severe impairment of respiratory function)
  • currently a smoker or quit less than 12 months ago

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placeboPlacebotwo capsules daily for 60 days
tart cherryPowdered tart cherrytwo capsules daily for 60 days
Primary Outcome Measures
NameTimeMethod
Change in fasting triglyceride levelsbaseline, 30 days post supplementation, 60 days post supplmentation
Change in baseline systolic and diastolic blood pressurebaseline, 60 days post supplmentation
Change in waist circumferencebaseline, 60 days post supplmentation
Change in erythrocyte sedimentation ratebaseline, 30 days post supplementation, 60 days post supplmentation
Change in fasting high-density lipoprotein (HDL) cholesterolbaseline, 30 days post supplementation, 60 days post supplmentation
Change in body fat distributionbaseline, 60 days post supplmentation
Change in fasting blood glucose levelbaseline, 30 days post supplementation, 60 days post supplmentation
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ohio University Exercise Physiology Lab

🇺🇸

Athens, Ohio, United States

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