Acceptability and Tolerance of a Protein and Micronutrient Fortified Food

University of California, Davis20 enrolled

Overview

Acceptability and tolerance of a new food product in adults and children.

Acceptability and tolerance testing will be conducted in 10 healthy male adult volunteers and 10 (40 - 60 years of age), and in children (9-13 years of age). All participants will be asked to consume 50g of a test product every day for 2 weeks for the adult volunteers, while the children will be asked to consume the same product every day for one week. The participants will record amount of daily intake, and will be given an entry and exit surveys. These surveys will include the assessment of potential gastrointestinal changes with daily product intake, and will include questions on how they liked the product. Acceptability will be measured as the number of servings and portion of serving completed each day over the trial period. In adults only, fasting blood samples and a spot urine will be collected towards preliminary work on potential changes in the metabolome and lipidome with the inclusion of the test product within the habitual diet.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Poor Nutrition

Interventions

Food Product 1OTHER

50 grams of fortified nutritious product from legumes

Eligibility

Sex: ALLMin age: 9 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

° Inclusion Criteria: * Male, 40-60 years old * Male or Female 9-13 years old * Subject is willing and able to comply with the study protocols * Subject is willing to consume the test products Exclusion Criteria: * Allergies or intolerances to peas, legumes, pulses, soy, dairy or wheat/gluten * Under current medical supervision * Non-English speaking * Self-reported history of cardiovascular disease, stroke, cancer, renal, hepatic, or thyroid disease, GI tract disorders, previous GI surgery * Currently taking prescription drugs or supplements * Daily use of aspirin and or non-steroidal anti-inflammatory medicines. * Indications of substance or alcohol abuse within the last 3 years * Any supplement use, including multi-vitamin/ mineral, herbal, plant or botanical, fish oil, and oil supplements. * Self-reported malabsorption * Current enrollee in a clinical research study.

Locations (1)

Department of Nutrition

Davis, California, United States

Outcomes

Primary Outcomes

GI function

GI function questionnaire with categorical numerical score

Time frame: at 2 weeks

Data from ClinicalTrials.gov

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