patientMpower for Idiopathic Pulmonary Fibrosis (IPF) provides the tools for patients to manage their treatment, get access to their medical data and help improve their outcome.
We empower patients with tools, data and information which is validated by their care team. Our platform connects with hospital systems allowing them to send data to patients and receive questions and
home measurements such as measuring their lung function. We are working with IPF Clinical centres and Researchers in Europe & USA.
Key benefits for patients include:
Track your Data
Record Forced Vital Capacity (FVC) and other lung measures with integrated home spirometry. Patients also log, Oxygen Saturation, Body Temperature and more.
Record Appointments & keep a Health Journal
Prepare for your appointments and record journal entries on anything related to your health (e.g. impact of breathlessness on your quality of life).
Help with your medications
Record your anti-fibrotic and any other medications and get reminders when to take them.
Complete Health Surveys
We are working with an academic partner in bringing the world’s first validated PROM for IPF patients – to understand disease progression and quality of life.
Set Exercise Goals
Set and track exercise goals, helping patients to improve their lung function with the support of their care team.
patientMpower curates content specific to IPF patients. We have videos available such as how to manage breathlessness, and have pulmonary rehabilitation videos in development.