Idiopathic Pulmonary Fibrosis is a devastating disease that ultimately leads to death. The median survival after diagnosis is 2-3 years with a continuous worsening of the disease (breathlessness, limited exercise capacity, need for oxygen). The cause of IPF is unknown. Individuals with IPF may experience symptoms such as breathlessness during activity, a dry and persistent cough, chest discomfort and finger clubbing. The disease is most common in males between 50 to 70 years old.

Completing a daily exercise routine within a pulmonary rehabilitation program (that also include disease education, nutrition and psychosocial support) has been shown to improve IPF patients mobility. However, outside of the hospital, it is difficult to keep IPF patients involved with the continuos exercise training and breathing techniques that can improve their quality of life. How can we prevent patients from becoming apathetic or forgetful about these routines?