Appetite Disorders Clinical Trial
— CMP2Official title:
Characterization of the Physiological and Subjective Satiety Response to Preloads Varying in Bioactive Dairy Proteins
Verified date | August 2017 |
Source | University of California, Davis |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Assessing 5 different milk derived proteins versus placebo for appetite regulation and satiety, delivered via shake vehicle.
Status | Completed |
Enrollment | 20 |
Est. completion date | September 2015 |
Est. primary completion date | May 2009 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Healthy - Unrestrained (score = 10 on the Eating Inventory (EI) questionnaire, Stunkard and Messick 1985) - Women - 18 years of age - Consume a low/moderate protein diet (12-20% protein energy). - Meet BMI criteria of 19 to 24 kg/m2 OR 29 to 34 kg/m2, inclusive. Exclusion Criteria: - Women who score = 10 on the Beck Depression Inventory (BDI, Beck and Beamesdorfer 1974) - Women who score = 30 on Eating Attitudes Test (EAT, Garner and Garfinkel 1979), - Have current or past (previous 1 year) medical conditions that may interfere with any of the outcomes of this study. - Weigh less than 110 lbs - Are currently or have been modifying diet or exercise patterns to gain or lose weight in previous 60 days - Have unstable body weight (fluctuations of = 5 kg in 60 day period) - Are excessive exercisers or trained athletes - Taking any medications that would affect appetite or any other study-described endpoint will also be excluded. - Allergies or intolerances to foods consumed in the study. - Smoker - Pregnant/lactation |
Country | Name | City | State |
---|---|---|---|
United States | University of California, Davis (Ragle Human Nutrition Research Center) | Davis | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Davis |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Post-prandial satiety | Blood biochemical markers of appetite regulation. | 6 hours | |
Primary | Post-prandial satiety | Assessing biobehavioral aspects of appetite regulation through VAS. | 6 hours | |
Secondary | Extended satiety | Utilizing self reported food intake, looking for changes associated with the different proetin compositions of the shakes. | 48 hours |
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