Asthma Data Innovation Demonstration Project (ADID)
Asthma, Bronchial Diseases, Respiratory Tract Diseases
About this trial
This is an interventional treatment trial for Asthma focused on measuring asthma, asthma control, healthcare utilization costs, community hotspots, public health research
Eligibility Criteria
Inclusion Criteria:
- Self-reported provider diagnosis of asthma
- Prescription for Short Acting Beta Agonist (SABA) at study intake
Exclusion Criteria:
- Subject is under the age of 5 at the beginning of the study
- Subject does not speak English
- Subject does not have access to the Internet or email to receive reports
- Subject has substantial co-morbidity (self-reported provider diagnosis of COPD)
Sites / Locations
- Jefferson County
Arms of the Study
Arm 1
Other
Propeller Health intervention group
All participants attached the Propeller sensor to their SABA medications and tracked the time and location of use for up to 13 months, to capture seasonal variation in medication use, symptoms and environmental triggers. The first 30-day run-in period served as a control period to assess levels of asthma control and SABA use; subject actuations were tracked, but participants and physicians did not receive their data or feedback. After the run-in period, participants received the full intervention for 12 months (see intervention for description).