The National Jewish Health is conducting a study on Symptoms and Activity in Pulmonary Fibrosis.
The medical field knows very little about how symptoms and activity levels change over time, or in response to supplemental oxygen use, in patients with PF.
The P₃F team (of patients, physicians, patient advocacy group representatives, PF support group leaders and others) wants to change this.
A real-world study of how symptoms and activity levels change in patients with pulmonary fibrosis (PF), from before to after daytime oxygen is initiated
By joining the P₃F team, you can help move the PF field forward by participating in this innovative research study!
- No travel required – not even to your doctor’s office
- Sign up is simple – just contact our study personnel to get started (click here for our contact information)
- You do not need a computer to participate but it helps if you have access to one with internet capabilities
- There is no cost to you or your insurance
Click on the link HERE to go to the website.