About this trial
This study aims to predict and minimize post-discharge adverse events (AEs) during care transitions through early identification and escalation of patient-reported symptoms to inpatient and ambulatory clinicians by way of predictive algorithms and clinically integrated digital health apps. We will (1) develop and prospectively validate a predictive model of post-discharge AEs for patients with multiple chronic conditions (MCC); (2) combine, adapt, extend, and iteratively refine our EHR-integrated digital health infrastructure in a series of design sessions with patient and clinician participants; (3) conduct a RCT to evaluate the impact of ePRO monitoring on post-discharge AEs for MCC patients discharged from the general medicine service across Brigham Health; and (4) use mixed methods to evaluate barriers and facilitators of implementation and use as we develop a plan for sustainability, scale, and dissemination.
Eligibility criteria
Qualifiers
Adult (18 years or older)
Hospitalized on the general medicine services at Brigham and Women's Hospital or Brigham and Women's Faulkner Hospital for at least 24 hours
Have a discharge status of home, home with services, or facility
English-speaking patients or their English-speaking legally designated healthcare proxy or next of kin (i.e., a family caregiver)
Disqualifiers
Less than 18 years of age
Less than two chronic conditions
Hospitalized less than 24 hours
No identifiable healthcare proxy or next of kin (i.e., a family caregiver)
Trial design
Treatments tested in this trial
- ePRO Application
Treatment groups
Sponsors and collaborators
Brigham and Women's Hospital
Lead sponsor
RAND
Collaborator