Contraction Timer ™ vs Kendamil Study

Track your contractions easily and stay informed. Contraction Timer™ helps you monitor your labor patterns with clarity and calm. Whether you’re timing your first contraction or in active labor, the clean, intuitive design makes it simple to log each contraction with a single tap. Why parents love Contraction Timer™ • One-Tap Tracking: Start or stop your timer instantly. • Smart Insights: View patterns for duration, frequency, and timing. • Simple, Distraction-Free Design: Focus on what matters most. • Steady Support: Stay organized and aware throughout your labor journey. • Share & Export Data: Easily send your contraction history to your care team or birth partner. Contraction Timer™ is designed to give you confidence and peace of mind as you prepare for your baby’s arrival. Join thousands of expecting parents who use Contraction Timer™ to track their progress and stay calm, focused, and ready. Terms & Conditions https://twistedsociety.github.io/ct-tos.html Privacy Policy https://twistedsociety.github.io/ct-pp.html Disclaimer Contraction Timer™ is not a medical device and does not replace professional medical advice. Always consult qualified healthcare professionals regarding any concerns about your pregnancy or labor.

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.