Introduction and Maintenance of Still Eating Protein Blends in Support of Infant Nutritional Goals

NCT ID: NCT03667118

Last Updated: 2019-03-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

705 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-06-18

Study Completion Date

2017-10-09

Brief Summary

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The purpose of the study is to test a food supplement to:

* Show that the food supplement is well tolerated and safe to feed to infants;
* Find out how often parents/caregivers feed their infants the food supplement;
* Find out how parents/caregivers usually add the food supplement to infants' regular solid or liquid food; and
* Learn what aspects of the food supplement are more or less attractive to infants and to parents/caregivers.

Detailed Description

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The study involves parents/caregivers of infants, ≥ 5 months but \< 11 months of age. Parents who enrolled their infants complete a 1-month blinded placebo run-in period, followed by randomization to placebo or the food supplement.

During the intervention period, infants randomized to the food supplement are fed a once daily, individual packet of the food supplement mixed into liquid (e.g., breast milk, infant formula) or solid (e.g., applesauce, pureed carrots) foods being fed to the infant. The food supplement is a blend of 16 common allergenic proteins (\[oat, milk, egg, sesame, wheat\] \[almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut\] \[cod, shrimp, salmon\]) combined with 400 IU of Vitamin D3. Parents complete a daily diary about any reactions or symptoms within 2 hours of ingesting the food supplement. Infants randomized to the placebo are also fed a once daily individual packet of the placebo mixed into liquid or solid foods being fed to the infant. Parents also complete a daily diary about any reactions or symptoms within 2 hours of ingesting the placebo.

Conditions

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Food Allergy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Participants
Parents received packets of the powder to be fed from their infant directly from the manufacturer.

Study Groups

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Food Supplement

Infants who received the active food supplement powder

Group Type EXPERIMENTAL

Food Supplement

Intervention Type DIETARY_SUPPLEMENT

A powder blend of 16 common allergenic proteins (\[oat, milk, egg, sesame, wheat\] \[almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut\] \[cod, shrimp, salmon\]) combined with 400 IU of Vitamin D3

Placebo

Infants who received the placebo powder

Group Type PLACEBO_COMPARATOR

Food Supplement

Intervention Type DIETARY_SUPPLEMENT

A powder blend of 16 common allergenic proteins (\[oat, milk, egg, sesame, wheat\] \[almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut\] \[cod, shrimp, salmon\]) combined with 400 IU of Vitamin D3

Interventions

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Food Supplement

A powder blend of 16 common allergenic proteins (\[oat, milk, egg, sesame, wheat\] \[almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut\] \[cod, shrimp, salmon\]) combined with 400 IU of Vitamin D3

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* healthy infants, ≥ 5 months but \< 11 months of age whose parent/caregiver can provide, in English, consent, understand instructions and complete a daily diet diary for their child, answer questions about how much and in what food they mix the Food supplement, and report any reaction or adverse event. Pregnant women will not be excluded if they have a child who is eligible for the study.

Exclusion Criteria

* \- Any parent/caregiver who cannot provide consent.
* Any parent/caregiver who cannot understand or write English.
* A parent/caregiver who is in prison.
* Any infant who

* Has a previous or current diagnosis of food allergy, made by a board-certified allergy and immunology specialist;
* Was born before 37 weeks of pregnancy (premature birth);
* Has severe eczema, as determined by two parent/caregiver questions:

1. During the past 6-11months, have you been told by a doctor or other health professional that your infant has eczema or any kind of skin allergy? (National Health Interview Survey, 2012) If yes, go to Question 2.
2. Would you describe (his/her) eczema or skin allergy as mild, moderate, or severe? (National Survey of Children's Health, 2007) If described as severe, infant is excluded.
* Has a current serious, chronic condition, as measured by:

1. Does you infant have a health condition that has lasted for more than three (3) months? If yes, go to Question 2.
2. Has your infant been hospitalized more than 2 times since birth for this condition? If yes to Question 1 and 2, infant is excluded.
* If a parent/caregiver has multiple birth infants (e.g., twins), only one eligible infant will be selected.
* Any person who works for Before Brands or who has a family member working for Before Brands.
Minimum Eligible Age

5 Months

Maximum Eligible Age

11 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Northwestern University

OTHER

Sponsor Role lead

Responsible Party

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Jane Holl

Director, Center for Healthcare Studies

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jane L Holl, MD MPH

Role: PRINCIPAL_INVESTIGATOR

Professor of Pediatrics, Feinberg School of Medicine

Locations

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Jane L Holl

Chicago, Illinois, United States

Site Status

Countries

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United States

Other Identifiers

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STU00205862

Identifier Type: -

Identifier Source: org_study_id

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