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Impact of 60 Days Powdered Tart Cherry Supplementation on Metabolic Syndrome

Impact of 60 Days Powdered Tart Cherry Supplementation on Metabolic Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05614947
Enrollment
25
Registered
2022-11-14
Start date
2022-04-06
Completion date
2025-07-25
Last updated
2025-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome

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.

Interventions

DIETARY_SUPPLEMENTPowdered tart cherry

500 mg freeze-dried tart cherry per capsule

DIETARY_SUPPLEMENTPlacebo

500 mg colored cornstarch per capsule

Sponsors

Ohio University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Change in baseline systolic and diastolic blood pressurebaseline, 60 days post supplmentation
Change in fasting high-density lipoprotein (HDL) cholesterolbaseline, 30 days post supplementation, 60 days post supplmentation
Change in fasting triglyceride levelsbaseline, 30 days post supplementation, 60 days post supplmentation
Change in fasting blood glucose levelbaseline, 30 days post supplementation, 60 days post supplmentation
Change in waist circumferencebaseline, 60 days post supplmentation
Change in body fat distributionbaseline, 60 days post supplmentation
Change in erythrocyte sedimentation ratebaseline, 30 days post supplementation, 60 days post supplmentation

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026