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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TERMINATED
NA
1 participants
INTERVENTIONAL
2017-10-03
2018-05-24
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
OTHER
QUADRUPLE
Study Groups
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Saturated Fat/SFA
30 grams saturated fat (SFA) in the form of heavy whipping cream will be provided to subject in a mixed meal shake
SFA
High saturated fatty acid/SFA oil source
Monounsaturated Fat/MUFA
30 grams monounsaturated fat (MUFA) in the form of olive oil will be provided to subject in a mixed meal shake
MUFA
High monounsaturated fatty acid/MUFA oil source
Polyunsaturated Fat Linoleic/PUFA
30 grams high linoleic polyunsaturated fat (PUFA) in the form of high linoleic sunflower oil will be provided to subject in a mixed meal shake
PUFA
High polyunsaturated fatty acid (linoleic)/PUFA oil source
Polyunsaturated Fat Omega-3/LCn3
30 grams high omega-3 polyunsaturated fat (LCn3) in the form of fish oil will be provided to subject in a mixed meal shake
LCn3
High polyunsaturated fatty acid (omega-3)/LCn3 oil source
Interventions
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SFA
High saturated fatty acid/SFA oil source
MUFA
High monounsaturated fatty acid/MUFA oil source
PUFA
High polyunsaturated fatty acid (linoleic)/PUFA oil source
LCn3
High polyunsaturated fatty acid (omega-3)/LCn3 oil source
Eligibility Criteria
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Inclusion Criteria
* free of major diagnosed, untreated medical conditions
* non-smoking or use of other tobacco products, including e-cigarettes
* not taking steroid-based medications
* not planning to or currently attempting to gain or lose weight
* willing to comply with study demands
* low intake of long chain omega-3 fatty acids (\<0.10 g/d) or willing to reduce intake for 6 weeks prior to starting the study
Exclusion Criteria
* diabetes (blood sugar ≥ 126 mg/dl)
* hypertension (systolic \> 160 mmHg or diastolic \> 100 mmHg)
* diagnosed cardiovascular, pulmonary, skeletal and metabolic diseases
* currently pregnant or planning to become pregnant, or lactating
* taking medications known to affect appetite, blood lipids, body composition, body weight, or food intake (appetite control drugs, steroids, antidepressants)
20 Years
55 Years
ALL
Yes
Sponsors
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USDA Grand Forks Human Nutrition Research Center
FED
Responsible Party
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Principal Investigators
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Susan Raatz, PhD
Role: PRINCIPAL_INVESTIGATOR
USDA Grand Forks Human Nutrition Research Center
Locations
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USDA Grand Forks Human Nutrition Research Center
Grand Forks, North Dakota, United States
Countries
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Other Identifiers
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GFHNRC509
Identifier Type: -
Identifier Source: org_study_id
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