The investigators will perform a parallel-group multicenter randomized controlled trial of a 1-year pre-enrolled acute hospital care at home intervention vs usual care for people living with dementia. Patients will be randomized only after eligibility determination and after the family caregiver agrees to enroll; people living with dementia will assent when able. Patients will be allocated in a concealed fashion to the control and intervention groups in randomly selected block sizes of 4 or 6 in 4 strata reflecting their functional status (activities of daily living: 0, 1, 2-3, 4-6). Although family and clinicians cannot be blinded, the investigators will blind the data collectors and assessors.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
200
Home visit for a serious illness conversation. Acute illness evaluation on demand. Acute hospital care at home as needed.
Standard acute and emergency care delivered in a brick-and-mortar hospital setting.
Brigham and Women's Hospital
Boston, Massachusetts, United States
Number of days at home
Sum of the number of days spent at home within the 30-days after an acute care episode
Time frame: Discharge to 30-days post discharge, up to 30 days
30-day unplanned readmission or mortality
Percentage of unplanned readmissions or mortality
Time frame: Discharge to 30-days post discharge, up to 30 days
Delirium
Percentage of days experiencing delirium while receiving acute care using the short confusion assessment method.
Time frame: Date of admission to date of discharge, estimated 5 days
Health-related quality of life
Absolute change of health-related quality of life over the year through the dementia quality of life survey (DEMQOL), or for patients unable to complete the survey, its proxy version (DEMQOL-Proxy).
Time frame: From enrollment for the period of one year
Physical activity
Percent of time sedentary as measured by patch monitoring system.
Time frame: Date of admission to date of discharge, estimated 5 days
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