Analysis of the Virtual Acute Care at Home Experience
Part of paid clinical trials in Peoria, Illinois.
- Sponsor
- OSF Healthcare System
- Study ID
- NCT05952999
- Status
- Enrolling By Invitation
Conditions
- Asthma, Chronic Obstructive Pulmonary Disease (COPD)
- Bronchitis
- Conditions
- Diabetes
- Fever
- Heart Failure
- Hypertension
- Infections
- Renal and Urinary Disorders
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Digital Care Solution as supportive personalized care — OTHERPatients will need to meet screening and inclusion criteria at time of enrollment. As a pragmatic study, researchers will not determine criteria or management of care aspects for patients.
- Traditional Hospital Level Care — OTHERPatients will be cared for in the inpatient setting for management of diseases that meet screening and inclusion criteria at time of enrollment for hospital at home. As a pragmatic study, researchers will not determine criteria or management of care aspects for patients.
Study Details
The purpose of this study is to examine the implementation, intervention effectiveness, and dissemination of a digital acute care delivery model for improving selected health outcomes in the Hospital at Home population.
Key Dates
- Start date
- Aug 15, 2023
- Status verified
- Mar 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 9,654 participants (estimated)
Arms
- Arm: Hospital at Home CareThe population for this study includes adult patients who are acutely ill and presenting to the emergency room, and are discharged to their home for hospital-level care in the home setting. The patients in this cohort may also include those who are discharged from the hospital early, but receive hospital-level care in the home setting.
- Arm: Traditional Hospital CareThe population for this study includes adult patients who are acutely ill and presenting to the emergency room who elect not to be discharged, choose to be cared for in the hospital setting.
Primary Outcome Measure
Composite of all-cause mortality for patients admitted to digital hospital [ Time Frame: Up to 30 days, (date of death from any cause, whichever came first, assessed up to 30 days) ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| OSF HealthCare | Peoria | Illinois | 61602 | - |
Find similar trials in Peoria, IL
By condition
By specialty
By research site
Related Studies
- The EMPOWER Trial - The Carillon Mitral Contour System® in Treating Heart Failure With FMRRecruiting · Cardiac Dimensions, Inc. · Gilbert, Arizona
- A Study Evaluating the Long-Term Efficacy and Safety of Ralinepag in Subjects With PAH Via an Open-Label ExtensionPHASE3 · Enrolling By Invitation · United Therapeutics · Phoenix, Arizona
- Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS)Recruiting · Duke University · Phoenix, Arizona
- Community Intervention to Reduce CardiovascuLar Disease in ChicagoRecruiting · Northwestern University · Chicago, Illinois