Acceptability and Tolerance of a Protein and Micronutrient Fortified Food

University of California (UC) Davis

Status: Completed

Conditions: Poor Nutrition

Treatments: Other: Food Product 1

Study type: Interventional

Funder types: Other

Identifiers

NCT03041103

985880

Details and patient eligibility

About

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

Full description

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.

Enrollment: 20 patients

Sex: All

Ages: 9 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

° 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.

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 2 patient groups

Adult

Experimental group

Description:

Food Product 1:50 grams of fortified nutritious product from legumes administered to adults, for 2 weeks

Treatment:

Other: Food Product 1

Children

Experimental group

Description:

Food Product 1: 50 grams of fortified nutritious product from legumes administered to children 9-13 years of age, for 1 weeks

Treatment:

Other: Food Product 1