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Casinomacropeptide and Satiety

Characterization of the Physiological and Subjective Satiety Response to Preloads Varying in Bioactive Dairy Proteins

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01587911
Acronym
CMP2
Enrollment
20
Registered
2012-04-30
Start date
2008-05-31
Completion date
2015-09-30
Last updated
2017-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lack of Satiety, Excess Intake of Macronutrients, Appetite Disorders

Keywords

Satiety, Food intake regulation, Appetite regulation, Dairy Protein

Brief summary

Assessing 5 different milk derived proteins versus placebo for appetite regulation and satiety, delivered via shake vehicle.

Detailed description

Assessing 5 different milk derived proteins versus placebo for appetite regulation and satiety, delivered via shake vehicle. Subjects will attend a 5 hour post-prandial study day. Subjects will keep food records 1 and 3 days prior to study visit, day of visit, and day after visit; food to be weighed using study provided dietary scale.

Interventions

OTHERWhey

Preload containing complete whey protein.

OTHERWhey-CMP

Preload containing complete whey protein which is missing the CMP/GMP portion of the protein.

OTHERControl

Preload control matched for energy to the other 5 preloads.

OTHERCMP

Preload containing the CMP (casinomacropeptide) portion cleaved from complete whey protein.

OTHERMPI

Preload containing whole milk protein.

OTHERCPI

Preload containing sodium caseinate.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Post-prandial satiety6 hoursBlood biochemical markers of appetite regulation.

Secondary

MeasureTime frameDescription
Extended satiety48 hoursUtilizing self reported food intake, looking for changes associated with the different proetin compositions of the shakes.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026