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N/A N=410 Health Services Research

Implementation of MIND at Home Into Primary Care for People Living With Dementia

Dementia

Enrolled (actual)
410
Serious AEs
27.6%
Results posted
Jan 2025
Primary outcome: Primary: Change in Number of Hospital Transfers Pre/Post Intervention — 0.97; 0.65; NA hospital transfers per 1000 person days

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
MIND at Home (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
American Medical Group Association
Primary completion
Apr 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Number of Hospital Transfers Pre/Post Intervention
0.97; 0.65; NA
SECONDARY
Change in Number of Medications Pre/Post Intervention
-0.43; 0.33; NA <0.05 sig

Summary

The number of people living with dementia (PLWD) is growing. PLWD are often cared for at home by an informal caregiver, but this care is often not sufficient, resulting in costly hospitalizations and other unnecessary and avoidable use of health services. In addition, many PLWD are transferred to costly long-term care facilities despite their preference to live at home. One way to improve care for PLWD is to work with their primary care doctors to provide better quality of care at lower costs for their patients. To accomplish this, we propose to collaboratively implement the MIND at Home Dementia Care Coordination Program into primary care clinics. The program expands the skills of existing primary care staff to the level of Memory Care Coordinators (MCCs), who will work with a larger primary care team on combining the benefits of clinic-based services with home-based services that support PLWD, their families, and care partners. Two health care organizations will enroll 150 people in the MIND at Home program for 3 months at a time. The program includes one home visit per month, a comprehensive needs assessment (which assesses medical, nonmedical, social, and environmental issues), the subsequent development and implementation of an individualized care plan, and unlimited contact with the MCC for the PLWD, their family, and care partner. The primary care team, including the MCC, will also have access to weekly virtual sessions focused on dementia and including short lectures and the discussion of specific case examples. Rates of monthly hospitalizations among participants and emergency room (ER) visits and number of medications the PLWD takes every month will be collected from the health care organization. The hypothesis is that the rate of hospitalizations and ER visits will decrease, and the number of medications will also decrease. We hope to positively impact the quality and costs of care associated with caring for PLWD. This pilot seeks to test the feasibility of implementing the MIND at Home program into primary care in a racially, ethnically, and geographically diverse population of PLWD to prepare for a larger study that will determine this program's effectiveness and spread it broadly into primary care clinics across the country. From the perspectives of health systems and overall society, MIND at Home will reduce costs, improve primary care team satisfaction, and preserve the dignity and independence of PLWD by enabling them to age at home.

Eligibility Criteria

Inclusion Criteria

  • Community residing adults, ≥18 years
  • People Living with Dementia (PLWD) defined by a diagnosis using algorithms based on CMS' Chronic Care Warehouse definition of Alzheimer's Disease, Related Dementias, Related Disorders, and Senile Dementia.11 This definition includes those who have an eligible diagnosis code on any eligible claim (i.e., inpatient, outpatient, skilled nursing facility (SNF), or home health visit or stay) in the past three years or a diagnosis on the patient problem list.
  • Actively receiving primary care services at one of three primary care practices within two participating health care organizations selected as study sites.
  • Have a reliable care partner who speaks English (or a language spoken by the Memory Care Coordinator).
  • Willing to participate in all study home visits and related activities for the entire length of the study (3 months).

Exclusion Criteria

  • PLWD in crisis, e.g., show signs of abuse, neglect, extreme risk of danger to self or others), will be connected to appropriate services, but will be excluded from the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05406921). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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