D-CARE - The Dementia Care Study: A Pragmatic Clinical Trial of Health System-Based Versus Community-Based Dementia Care

NCT03786471 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2176

Last updated 2025-01-30

Study results available
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Summary

D-CARE: The Dementia Care Study

This pragmatic randomized clinical trial of 2150 persons with dementia and their caregivers, at four diverse clinical trial sites in the United States, compares the effectiveness and cost-effectiveness of 18 months of health systems-based dementia care provided by a Dementia Care Specialist (nurse practitioner or physician assistant) who works within the heath system versus community-based dementia care provided by a Care Consultant (social worker, nurse, or therapist) who works at a Community-Based Organization (CBO).

The trial will also compare the effectiveness and cost-effectiveness of both models versus usual care.

Conditions

Interventions

OTHER

Health System-based Dementia Care

Active comparator

OTHER

Community-based Dementia Care

Active comparator

OTHER

Usual Care

Control

Sponsors & Collaborators

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER
  • National Institute on Aging (NIA)

    collaborator NIH
  • Yale University

    collaborator OTHER
  • Benjamin Rose Institute on Aging

    collaborator OTHER
  • Baylor Scott and White Health

    collaborator OTHER
  • Wake Forest University Health Sciences

    collaborator OTHER
  • University of Texas

    collaborator OTHER
  • Geisinger Clinic

    collaborator OTHER
  • University of Oklahoma

    collaborator OTHER
  • RAND

    collaborator OTHER
  • University of California, Los Angeles

    lead OTHER

Principal Investigators

  • David Reuben, MD · University of California, Los Angeles

  • Thomas Gill, MD · Yale University

  • David Bass, PhD · Benjamin Rose Institute on Aging

  • Lee Jennings, MD · University of Oklohoma

  • Maya Lichtenstein, MD · Geisinger Clinic

  • Peter Peduzzi, PhD · Yale University

  • Alan Stevens, PhD · Baylor Scott and White Health

  • Elena Volpi, MD, PhD · The University of Texas Health Science Center at San Antonio

  • Jeffrey Williamson, MD · Wake Forest University Health Sciences

  • Christopher Callahan, MD · Indiana University

  • Katie Maslow, MSW · Gerontological Society of America

  • Jenny Summapund, MA · University of California, Los Angeles

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-28
Primary Completion
2023-08-21
Completion
2023-08-21

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03786471 on ClinicalTrials.gov