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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05766956
Other study ID # 22-013387
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date July 10, 2023
Est. completion date June 2024

Study information

Verified date August 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare two care delivery models that are currently being implemented in routine practice settings. The findings from this study will inform future clinical decision making, such as which patients might be more suited for which care delivery model.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 360
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients, 18 years of age and older - Present to one of the participating hospitals - Have a chief complaint of one of the target diagnoses - Are within a certain geographical area (based on zip codes) - Have a health insurance plan that covers ACH services - Have the capacity to consent or could assent with the consent of a health care proxy who is physically present Exclusion Criteria: - Not suitable for ACH or inpatient hospital care as determined by the patient's clinical team - Do not have the capacity to consent or assent with the assistance of a health care proxy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Advanced Care at Home (ACH)
Inpatient hospitalization offered in the home setting.
Traditional Brick-and-Mortar Hospitalization
Inpatient hospitalization offered in the hospital setting.

Locations

Country Name City State
United States Mayo Clinic Health System Eau Claire Wisconsin
United States Mayo Clinic Jacksonville Jacksonville Florida
United States Mayo Clinic Arizona Phoenix Arizona
United States Mayo Clinic Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The primary outcome is a composite outcome of all-cause mortality The rate of death 30 days post-discharge
Primary 30-day readmission Readmission between discharge from ACH/traditional inpatient hospital care and 30 days post-discharge 30 days post-discharge
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