ClinicalTrials.Veeva

Menu

Improving How People Living With Dementia Are Selected for Care Coordination

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status

Completed

Conditions

Dementia

Treatments

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

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05651308
3U54AG063546-03 (U.S. NIH Grant/Contract)
Subaward 00002102 (Other Grant/Funding Number)
22-10025292

Details and patient eligibility

About

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.

Full 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.

Enrollment

385 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

385 participants in 2 patient groups

Intervention
Experimental group
Description:
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.
Treatment:
Behavioral: Care coordination delivered based on perceived need
Control
Active Comparator group
Description:
Usual care assigns patients to care coordinators in response to a discharge from a hospital or a direct referral from a physician.
Treatment:
Behavioral: Care coordination delivered based on usual care (e.g. discharge from hospital)

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems