Skip to main content
Clinical Trials/NCT05651308
NCT05651308CompletedNot Applicable

Improving How People Living With Dementia Are Selected for Care Coordination: A Pragmatic Clinical Trial Embedded in an Accountable Care Organization

Weill Medical College of Cornell University1 site in 1 country385 target enrollmentStarted: December 5, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
385
Locations
1
Primary Endpoint
Number of Emergency Department Visits or Hospital Admissions

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Intervention

Experimental

The intervention group will assign care coordinators to PLWD based on perceived need for assistance with care coordination. Perceived need will be measured through a proxy's responses to a previously validated telephone survey on perceptions of care coordination.

Intervention: Care coordination delivered based on perceived need (Behavioral)

Control

Active Comparator

Usual care assigns patients to care coordinators in response to a discharge from a hospital or a direct referral from a physician.

Intervention: Care coordination delivered based on usual care (e.g. discharge from hospital) (Behavioral)

Outcomes

Primary Outcomes

Number of Emergency Department Visits or Hospital Admissions

Time Frame: Over 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 Outcomes

  • Efficiency(Up to 1 year)
  • Acceptability(Up to 1 year)
  • Appropriateness(Up to 1 year)
  • Fidelity(Up to 1 year)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials