← Back to all trials
Completed
NCT05568043
The Reducing REVISITS Study: A Cluster RCT
Conditions: COPD, COPD Exacerbation Acute
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 384
Sponsor: University of Chicago
Location: University of Chicago Chicago Illinois
Summary
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.
Eligibility Criteria
Since enrollment for Aim 2 will occur on a site/system-level, the inclusion of specific individuals who meet these criteria are not applicable since Aim 2 will only enroll hospital sites, not individuals. The sites the investigators enroll will represent diverse patient populations and geographical locations across the US.
Source: ClinicalTrials.gov (NCT05568043). StuddyBuddy aggregates publicly available trial information.