Effects of Dietary Protein Intake From Beef/Pork and Soy/Legumes on Appetite, Mood, and Weight Loss - NCT01005563-47907(Clinical Trial 709324)
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W Lafayette |
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State:
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IN |
| Zip Code: |
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47907 |
| Conditions: |
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Appetite - Mood - Weight Loss |
| Purpose: |
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The primary aims of this study are to assess the effects of habitual dietary protein intakes
across the acceptable macronutrient distribution range with lean beef/pork or soy/legumes as
the predominate sources of protein on indices of daily appetite and mood, and on
postprandial appetite, mood, energy expenditure, and glycemic responses during
energy-restricted weight loss in overweight adults.
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| Study summary: |
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| Criteria: |
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Inclusion Criteria:
- Age range: 21 years and older
- Body mass index between 27.0-36.9 kg/m2
- Non-smoking (within the last 6 months)
- Weight stable (< 3 kg (~7 lbs) weight gain or loss within last 3 months)
- Energy need for weight maintenance 1950-2750 kcal/day
- Not dietary restrained
- Menstruating women not pregnant or lactating
- Constant habitual activity patterns (within last 3 months)
- No Acute Illness (or have chronic diseases known to influence protein or energy
metabolism)
- Non-diabetic
- Clinically normal blood profiles (within 10% of clinical normalcy)
- Non-hypertensive
- Not taking medications known to influence appetite or metabolism
- Willingness to eat study foods
- Able to travel to testing facility
Exclusion Criteria:
- Age: <21 years
- Body mass index: outside of the 27.0-36.9 kg/m2 range
- Smoker (currently or within the last 6 months)
- Gained or lost > 3.0 kg (7 lbs) within the last 3 months
- Energy need for weight maintenance < 1950 or > 2750 kcal/day
- Dietary restrained (≥ 14 on Three Factor Eating Questionnaire)
- Pregnant, lactating, or non-menstruating women
- Clinically diagnosed as a diabetic, or with liver or kidney disease/dysfunction, or
osteoporosis
- Clinically abnormal blood profiles as identified by our study physician, Arthur
Rosen, MD
- Hypertensive
- Taking medications (currently or within the last 3 months) known to influence
appetite or metabolism
- Allergies to eggs
- Lactose intolerance
- Unwillingness to eat study foods
- Inability to travel to testing facility |
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| Study is available at: |
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Purdue University W Lafayette, IN 47907 United States
Primary Contact: Jan Green Email: jkgreen@purdue.edu Phone: 765-496-6342 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
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