Education with or without reminders for continued peanut feeding after supervised introduction in infants

You may qualify if

• Caregivers:
• You are 18 years old or older.
• You are the infant's parent or legal guardian.
• You are able to give permission for yourself and your infant to participate in the study.
• You can speak and read English.
• You are interested in introducing peanut-containing foods to your infant and continuing to feed peanut regularly.
• You are willing to attend the supervised peanut feeding event and complete study follow-up activities.
• You are willing to receive study-related reminders and communications by phone, email, or text message.
• Infants:
• They are 4 to 8 months old at the time they join the study.
• They are developmentally ready to safely eat foods by mouth.
• They have never eaten peanut before.
• The study team determines that they are an appropriate candidate for supervised peanut introduction.
• Advisory Panel Participants:
• You are 18 years of age or older.
• You are able to provide informed consent.
• You have experience related to one or more of the following: Community feeding events, Behavioral interventions, Pediatric allergy care, Community medical practice, Implementation or program development, Health equity, Participant recruitment and retention, Community engagement
• You are willing to participate in a virtual discussion group or feedback session that may be audio recorded.

You can't join if

• Caregiver-Infant Pairs
• The infant has already eaten peanut.
• The infant has a known peanut allergy or has been diagnosed with a peanut allergy by a doctor.
• The infant has had a previous reaction that may have been caused by a peanut allergy.
• The infant has a diagnosed feeding disorder.
• The infant has a medical, developmental, or feeding condition that could make peanut introduction unsafe or make it difficult to participate in the study.
• The caregiver is not the infant's parent or legal guardian.
• The caregiver is unable or unwilling to provide consent for participation.
• The caregiver is unable to participate in study activities and follow-up assessments in English.
• The caregiver or infant has another condition or circumstance that the study doctor believes would make participation unsafe, impractical, or not in their best interest.
• Advisory Panel Participants:
• You are unable or unwilling to provide informed consent.
• You are unable to participate in the virtual discussion group or feedback session.
• The study team determines that a conflict of interest, role limitation, or other circumstance makes participation inappropriate.