PatientWing Blog

PatientWing is thrilled to be attending the 16th Annual Summit for Clinical Ops Executives (SCOPE) in sunny Orlando, Florida, from February 3rd to 6th! 🌞

Trust is the foundation of any meaningful relationship, especially when engaging patients in clinical studies. At its core, trust means having confidence in someone—believing they are genuine, sincere, and have your best interests at heart. It’s also about knowing that the information you receive is reliable and truly trustworthy. For patients living with rare diseases and serious conditions, trusting the people and process behind a clinical study can make all the difference.

In clinical research, finding the right participants for a study is like solving a puzzle. But the puzzle is more complex than just matching patients to trials—it involves earning their trust, understanding their needs, and helping them overcome barriers to participation. This is where advocacy partnerships come in.

If you’re reading this, you may be considering participating in a clinical study. This is an exciting step in your health journey, but it’s crucial you ensure your rights, safety, and well-being are protected throughout the research process. Advocating for yourself and your health is vital to ensure you get the care you need and deserve.