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Improving Access to Care for Veterans With Memory Loss

V

Veterans Affairs (VA) Pittsburgh Healthcare System

Status

Enrolling

Conditions

Alzheimer Disease

Treatments

Other: ADRD Care Delivery Protocol

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT07117162
1850695

Details and patient eligibility

About

This study evaluates a care delivery protocol to improve access to care for Veterans with Alzheimer's Disease and Related Disorders (ADRD). A randomized controlled trial will enroll Veterans with mild cognitive impairment or early dementia at VA Pittsburgh. The ADRD care delivery protocol integrates telehealth, advanced diagnostics, and streamlined workflows to expedite screening for eligibility for amyloid targeting therapies.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of mild cognitive impairment or mild dementia due to suspected or confirmed AD with a 5 minute telephone MoCA score >7
  • Meets VA MUE inclusion/exclusion criteria for mAb therapy for AD
  • Enrolled in VA care
  • Lives in a home setting (i.e., not in an institutional setting such as a nursing home, Community Living Center, or hospital)
  • Has a working telephone
  • 18 years and older
  • Able to communicate in English
  • Willing to give informed consent.

Exclusion criteria

  • None

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 2 patient groups

ADRD Care Delivery Protocol
Experimental group
Description:
Patients will undergo telehealth preparedness assessment, cognitive screening, and blood biomarker testing prior to the initial consultation with the specialist.
Treatment:
Other: ADRD Care Delivery Protocol
Usual Care
No Intervention group
Description:
Patients will undergo usual care with all evaluation and testing at the discretion of the specialist.

Trial contacts and locations

1

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Central trial contact

Julie Faieta, PhD; Alison O'Donnell, DO, MPH

Data sourced from clinicaltrials.gov

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