This type II hybrid effectiveness-implementation trial will concurrently study the comparative effectiveness of virtual vs. in-person COPD care transition programs implemented via virtual mentored implementation approaches with and without co-design methods. The investigators will enroll up to 24 randomized sites (with a goal minimum of 16 sites) to: * Deliver the COPD programs implemented via mentored support in collaboration with SHM Center for Quality Improvement. * Compare the effectiveness and penetration of virtual versus in-person COPD care transition programs implemented along with mentoring support with or without co-design. The investigators aim to determine which combined approach(es) is/are the most effective at implementing evidence-based COPD program interventions and decreasing COPD acute care revisits with the greatest overall impact and sustainability.
Age range
18 Years
Sex
ALL
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A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Healthcare Utilization: 30-day acute care revisits for COPD
Timeframe: Immediately Post-Program Implementation (12 months after enrollment in Aim 2)
Delivery of overall care transition program: penetration
Timeframe: Immediately Post-Intervention (12 months after enrollment in Aim 2)
Sustainability of effectiveness: 30-day revisits
Timeframe: Quarterly for 24 months Post-Intervention initial enrollment (Aim 3)
Sustainability of program delivery: penetration
Timeframe: Quarterly for 24 months Post-Intervention initial enrollment (Aim 3)