Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
19 participants
INTERVENTIONAL
2023-05-13
2024-05-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
SINGLE
Study Groups
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Intervention Treatment
Experimental treatment will contain a cereal product that contains a dietary fiber. This will be consumed three times daily for two weeks.
Fiber
The intervention treatment will contain fiber.
Control treatment
Control treatment will contain a corn meal cereal product that will be consumed three times daily for two weeks.
Control
The control treatment will contain corn meal.
Interventions
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Fiber
The intervention treatment will contain fiber.
Control
The control treatment will contain corn meal.
Eligibility Criteria
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Inclusion Criteria
* BMI between 18.5 and 39.9 kg/m2
* Ability to drop-off 1 fecal sample within 15 minutes of defecation
* Ability to pick-up meals daily
* Ability to collect fecal and urine samples daily
* Fasting glucose of \<126 mg/dL
Exclusion Criteria
* Any food allergies or intolerances
* Prior diagnosis of metabolic or gastrointestinal disease (kidney disease, liver disease, gout, hyperthyroidism, untreated or unstable hypothyroidism, certain cancers, gastrointestinal disease, pancreatic disease, diabetes requiring medication)
* Women that are pregnant, had a baby within the last 12 months, or are 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
* History of malabsorptive or restrictive bariatric surgeries (e.g., gastric bypass, sleeve gastrectomy, adjustable gastric band) or gall bladder removal surgery
* Are unable or unwilling to consume the experimental meals/snacks.
* Taking certain medications (Orlistat, bile binding resins, insulin, oral hypoglycemic agents, laxatives)
* Concurrent enrollment in another dietary, exercise, or medication study
22 Years
75 Years
ALL
Yes
Sponsors
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University of Illinois at Urbana-Champaign
OTHER
Responsible Party
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Locations
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Edward R Madigan Laboratory
Urbana, Illinois, United States
Countries
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Other Identifiers
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24042
Identifier Type: -
Identifier Source: org_study_id