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Increasing Access to Care: An Advanced Virtual Care Delivery Protocol to Deliver Diagnostic and Therapeutic Services to Underserved Veterans With ADRD

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
United States
Pennsylvania
VA Pittsburgh Healthcare System
RECRUITING
Pittsburgh
Contact Information
Primary
Alison O'Donnell, DO, MPH
alison.odonnell2@va.gov
412-522-3123
Backup
Julie Faieta, PhD
juf52@pitt.edu
Time Frame
Start Date: 2025-10-29
Estimated Completion Date: 2027-06
Participants
Target number of participants: 30
Treatments
Experimental: ADRD Care Delivery Protocol
Patients will undergo telehealth preparedness assessment, cognitive screening, and blood biomarker testing prior to the initial consultation with the specialist.
No_intervention: Usual Care
Patients will undergo usual care with all evaluation and testing at the discretion of the specialist.
Related Therapeutic Areas
Sponsors
Leads: VA Pittsburgh Healthcare System

This content was sourced from clinicaltrials.gov