MedPath

Improving How People Living With Dementia Are Selected for Care Coordination

Not Applicable
Completed
Conditions
Dementia
Registration Number
NCT05651308
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

Many people living with dementia (PLWD) and their care partners may benefit from the assistance of a care coordinator, a member of the medical team who facilitates communication among all the people involved. However, care coordinators' time is limited, and there is uncertainty about which patients should be selected to receive their help. This pragmatic clinical trial embedded in an accountable care organization will determine the comparative effectiveness of two approaches for assigning care coordinators to PLWD.

Detailed Description

This project will use a pragmatic clinical trial embedded in an accountable care organization (ACO) to determine the comparative effectiveness of two different approaches for selecting PLWD to receive support from care coordinators: (1) an approach that assigns PLWD to care coordinators based on care partners' self-reported difficulty with care coordination, or (2) usual care, which generally assigns PLWD to care coordinators after hospital discharge, regardless of perceived need. The investigators will include community-dwelling Medicare beneficiaries ≥65 years old with dementia who have been attributed to the NewYork Quality Care ACO and who have fragmented care. The investigators will randomize the participants into two groups. This study is highly pragmatic, and the intervention is sustainable and scalable. Moreover, the proposed approach has the potential to improve care delivery and outcomes for PLWD.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
385
Inclusion Criteria
  • Medicare beneficiaries ≥65 years old who:
  • Are attributed to the NewYork Quality Care accountable care organization by Medicare,
  • Have dementia (as measured in claims using the Bynum standard 1-year definition),
  • Reside in the community, and
  • Had fragmented ambulatory care in the previous 12 months (defined as a reversed Bice-Boxerman Index greater than or equal to the median score for this population, using Medicare claims)
Exclusion Criteria
  • Those who reside in long-term care or nursing home facilities (based on addresses in Medicare claims), or
  • Enrolled in home hospice

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Number of Emergency Department Visits or Hospital AdmissionsOver 12 months (beginning 1 month after the start of care coordination)

Occurrence of an emergency department visit or hospital admission, as measured in Medicare claims

Secondary Outcome Measures
NameTimeMethod
AcceptabilityUp to 1 year

The number of people who accepted care management in each group

AppropriatenessUp to 1 year

The number of people with problems in scope for care coordinators, out of all people who received care management

FidelityUp to 1 year

The number of people who actually received care coordination services, out of all of those who agreed to receive it

EfficiencyUp to 1 year

The number of care coordinator encounters in each group. This measure allows more than one encounter per person.

Trial Locations

Locations (1)

New York Presbyterian Hospital - Weill Cornell Medicine

🇺🇸

New York, New York, United States

New York Presbyterian Hospital - Weill Cornell Medicine
🇺🇸New York, New York, United States

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.