Real-time Symptom Monitoring Using ePROs to Prevent Adverse Events During Care Transitions
Recruiting
N/A
Interventional Study
Multiple Chronic Conditions
Adverse Event
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 1,300 (estimated)
- Sponsor
- Brigham and Women's Hospital · Other
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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 mul…
Trial Locations
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Eligibility 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 Engl…
Contacts