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Clinical Trials/NCT05952999
NCT05952999
Enrolling by Invitation
N/A

Examining the Intervention Effectiveness of Hospital at Home for Improving Health Outcomes and Experiences for Patients, Clinicians, and Caregivers

OSF Healthcare System1 site in 1 country9,654 target enrollmentAugust 15, 2023

Overview

Phase
N/A
Intervention
Digital Care Solution as supportive personalized care
Conditions
Conditions
Sponsor
OSF Healthcare System
Enrollment
9654
Locations
1
Primary Endpoint
30-day readmission rate
Status
Enrolling by Invitation
Last Updated
last month

Overview

Brief Summary

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.

Detailed Description

The investigators will conduct a mixed-methods quasi-experimental research study that will explore the effectiveness of the Hospital at home programs using qualitative interviews and quantitative data as a means to also conduct a process evaluation related to the implementation and efficacy of Hospital at Home programs. The purpose of this pragmatic study is to inform scalability beyond the initial site for implementation within a large healthcare system with a diverse patient population located in various communities, including rural and urban locations.

Registry
clinicaltrials.gov
Start Date
August 15, 2023
End Date
December 31, 2026
Last Updated
last month
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Colleen J Klein

Education & Research Scientist, Center for Advanced Practice, Principal Investigator

OSF Healthcare System

Eligibility Criteria

Inclusion Criteria

  • Patients 18 years and older who are admitted into the Hospital at Home program after presenting to the emergency department or who are inpatients that can be cared at home for hospital level needs
  • Patients meeting the hospital's criteria for admission by diagnosis type (e.g., heart failure, respiratory infections and inflammations, renal failure, diabetes, pneumonia, bronchitis, chronic obstructive pulmonary disease, fever and inflammatory conditions, viral illnesses, other disorders of the nervous system). Diagnoses are determined by clinicians not researchers.
  • Patients will need to reside within 30 minutes' drive time from the hospital
  • Patient caregiver inclusion criteria: (not required for patient participation):
  • Age \>= 18 years old
  • as capacity to consent to study
  • Clinician or stakeholder inclusion criteria:
  • Any member of the home hospital clinical team (a healthcare professional who providing care or equipment for use in the home) who will be participating in delivery of healthcare services,
  • Any member of the hospital care teams, including the screening and recruitment of patients for the home hospital intervention and/or providing care to patients that enroll in the intervention that is provided
  • Any member of the leadership team who are involved in the operational aspects of program delivery

Exclusion Criteria

  • Need for long-term facility level care or current residence in a facility of this type
  • No one will be excluded on the basis of sex or race

Arms & Interventions

Hospital at Home Care

The 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.

Intervention: Digital Care Solution as supportive personalized care

Traditional Hospital Care

The 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.

Intervention: Traditional Hospital Level Care

Outcomes

Primary Outcomes

30-day readmission rate

Time Frame: Up to 30 days (date of readmission from any cause, whichever came first, assessed up to 30 days)

Number of 30-day readmissions as defined by Organization using preset criteria

Patient Satisfaction at discharge

Time Frame: up to 1 week

1-item measure: I would recommend this \[insert program name\] to others, assessed at discharge name\] to others.

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)

Total number of deaths over total number of patients admitted to the digital hospital.

Patient Perception of Digital Care at discharge

Time Frame: up to 1 week

Results of Digital Care - Likert Scale (very satisfied to very dissatisfied)

Secondary Outcomes

  • Unplanned readmission within 30-days of discharge(up to 30 days)
  • Length of Stay(assessed up to 2 weeks)
  • Number of participants with Hospital Acquired Infections(assessed up to 1 week)
  • Escalations (for management and treatment of early decompensation)(up to 2 weeks)

Study Sites (1)

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