Real-time Symptom Monitoring Using ePROs to Prevent Adverse Events During Care Transitions
Sponsor: Brigham and Women's Hospital
Trial Details
| Condition | Multiple Chronic Conditions, Adverse Event |
| Intervention | ePRO Application |
| Phase | NA |
| Status | Recruiting |
| Participants | 1,300 |
| Est. Completion | 15 Sept 2026 |
| Last Updated | 20 Apr 2026 |
Primary Outcome
Actual adverse events (AEs); Actual preventable adverse events (AEs)
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: * 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) * Non-English-speaking patients who have an English-speaking legally designated healthcare proxy or next of kin (i.e., a family caregiver) * Two or more chronic conditions: Anxiety, Asthma\*, Arthritis (Osteoarthritis, Rheumatoid), Atrial Fibrillation, Cancer\*, Cerebral vascular accident, Chronic kidney disease\*, Chronic obstructive pulmonary disease (COPD)\*, Cirrhosis, Coronary artery disease/Ischemic heart disease, Dementia, Depression, Diabetes mellitus\*, End-stage renal disease\*, Heart failure\*, Hepatitis B, C\*, HIV/AIDs, Hyperlipidemia, Hypertension, Inflammatory bowel disease, Osteoporosis, Sickle cell disease, Substance abuse (Alcohol/Opioid) Exclusion Criteria: * 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 Sites
Countries
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