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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COMPLETED
NA
22 participants
INTERVENTIONAL
2014-01-31
2018-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Inulin
Participants will receive 10 g of inulin powder each day for 6 weeks.
Inulin
The treatment will be mixed in orange juice or other beverage and will be consumed at breakfast each day in our metabolic kitchen.
Placebo
Participants will receive 10 g of maltodextrin each day for 6 weeks.
Placebo
The placebo will be mixed in orange juice or other beverage and will be consumed at breakfast each day in our metabolic kitchen.
Interventions
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Inulin
The treatment will be mixed in orange juice or other beverage and will be consumed at breakfast each day in our metabolic kitchen.
Placebo
The placebo will be mixed in orange juice or other beverage and will be consumed at breakfast each day in our metabolic kitchen.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Fasting glucose between 5.6 - 6.9 mmol/L and/or a 2h plasma glucose between 7.8-11.1 mmol/L following a 75 g oral glucose tolerance test.
* Weight stable for previous 6 months (+/- 2.0 kg).
* Sedentary to recreationally active
* Willing to be randomized to treatment or placebo.
* Verbal and written informed consent.
* No plans to gain/lose weight or change physical activity level.
* Willing to pick up food daily, and consume foods provided for the 6-week controlled feeding period.
Exclusion Criteria
* Diabetes or diabetes medications
* Prebiotic or probiotic supplement or product consumption in prior 3 months.
* Total cholesterol \> 6.2 mmol/L; triglycerides \> 4.5 mmol/L.
* Blood pressure \> 140/90 mmHg or antihypertensive medications.
* Diagnosed inflammatory disease (e.g. lupus, irritable bowel, periodontal disease, etc)
* Fructo, galacto-, xylo-oligosaccharide intake \> 3 g/day.
* Past or current ischemic heart disease, stroke, respiratory disease, endocrine or metabolic disease, neurological disease, or hematological-oncological disease.
* Smoking, alcohol consumption \> 2 servings /d for males and 1 serving/d for females, or taking medications (including but not limited to statins or other drugs with anti-inflammatory actions) or antioxidant vitamins or supplements.
* Known allergy, hypersensitivity, or intolerance to inulin.
40 Years
70 Years
ALL
No
Sponsors
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Virginia Polytechnic Institute and State University
OTHER
Responsible Party
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Kevin Davy
Kevin P. Davy, PhD
Principal Investigators
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Kevin P Davy, PhD
Role: PRINCIPAL_INVESTIGATOR
Virginia Polytechnic and State University
Locations
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Virginia Polytechnic and State University
Blacksburg, Virginia, United States
Countries
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Other Identifiers
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Prebiotics-Prediabetes
Identifier Type: -
Identifier Source: org_study_id
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