Status:

UNKNOWN

Walnut Consumption and Gut Microbiota

Lead Sponsor:

University of Illinois at Urbana-Champaign

Conditions:

Obesity

Inflammation

Eligibility:

All Genders

25-75 years

Phase:

NA

Brief Summary

Obesity is a growing health issue that effects the majority of adults in the United States. Prevalence of other metabolic diseases are increased in obese adults, including systemic inflammation. There...

Eligibility Criteria

Inclusion

  • Participants will include adults ages 25-75 years BMI of \> 30 kg/m2 Ability to drop-off fecal sample within 15 minutes of defecation

Exclusion

  • Walnut allergy or intolerance
  • Food allergies or intolerances
  • Prior diagnosis of metabolic or gastrointestinal disease (cardiovascular disease and type 1 or type 2 diabetes, chronic constipation, diarrhea, Crohn's disease, celiac disease, ulcerative colitis, irritable bowel syndrome, diverticulosis, stomach or duodenal ulcers, hepatitis, HIV, cancer, etc.)
  • Women that are pregnant, had a baby within the last 12 months, or lactating
  • Individuals that smoke, use tobacco, abuse drugs, or consume \> 2 alcoholic beverages per day.
  • \> 5% weight change in the past month or \> 10% change in the past year
  • Oral antibiotics during the previous 6 weeks
  • Fasting blood glucose \>126 mg/dL, blood pressure \>160/100 mm Hg, elevation in serum transaminases (i.e. \>3 times the upper limit of normal) or with evidence of liver disease, including primary biliary cirrhosis or gallbladder disease, constipation, are currently taking lipid-lowering medications, oral hypoglycemic agents, or insulin, or certain medications (laxatives, bile acid sequestrants, and opiates)
  • History of malabsorptive or restrictive bariatric surgeries (e.g., gastric bypass, sleeve gastrectomy, adjustable gastric band) or gall bladder removal surgery.
  • Are unable to consume the experimental meals/snacks.
  • Participants who have donated blood within the last 8 weeks
  • Recent diagnosis of anemia
  • Concurrent enrollment in another dietary, exercise, or medication study

Key Trial Info

Start Date :

June 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2024

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT05441748

Start Date

June 1 2022

End Date

July 1 2024

Last Update

June 18 2023

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Hannah Holscher

Urbana, Illinois, United States, 61801