Pacify vs Kendamil Study

Pacify connects you with trusted doulas and lactation consultants, offering flexible support to guide you through every stage of pregnancy and postpartum with 1:1 video, chat and in-person care. Subscribe to one of our plans, sign up with a health plan or employer code, or easily check to see if your insurance covers Pacify at no cost to you and gain access to features like: * Doula care to prep for labor, provide birth support and ease postpartum recovery * On-demand and scheduled virtual infant feeding support with lactation consultants * Scheduled virtual care or in-person care (in select areas) * Direct chat messaging with your care team and care coordinator * Educational articles and videos in the Pacify library * Spanish language app and Spanish-speaking providers available Pacify Health is committed to protecting your privacy. Provider consultations are always private, secure, and HIPAA compliant. The features available to you depend on your coverage and plan.

Welcome to the Kendamil Study: The Kendamil app is a proprietary platform of ObvioHealth being used to manage a trial to study use of an investigational infant formula and how it affect infant growth and tolerance in comparison to current market formula. The Kendamil app removes the costly overhead of physical site visits and brings the trial directly to the mobile device of each subject. The result? Robust data collection, increased compliance, faster time to completion, and average cost savings of ~50% vs. traditional on-site trials. Subject Journey A subject who is identified as eligible for this study during pre-screening will be invited to download the Kendamil App via e-mail. Upon download, the participants create an account and complete the Informed Consent process. A series of screens explains the parameters of the study, including: o Privacy Policy o Data Gathering & Usage o Study Tasks & Surveys o Time Commitment o Option to Withdraw Subjects will have the opportunity to connect with a member of the study team to ask questions prior to signing the informed consent form. Intervention Period: Daily Tasks Subjects will contribute data to the study by completing questionnaires and data uploads over a 7-day baseline period and 16-week active trial period. Subjects can interact with the study team via secure chat as needed.