Reducing Risk of Dementia Through Deprescribing

NAActive, not recruitingINTERVENTIONAL
Enrollment

344

Participants

Timeline

Start Date

July 20, 2020

Primary Completion Date

July 30, 2026

Study Completion Date

July 30, 2026

Conditions
DementiaAlzheimer Disease, Late Onset
Interventions
OTHER

Deprescribing of target anticholinergics

The active intervention group (ACT) will receive a pharmacist-based deprescribing intervention focused only on targeted anticholinergic medications. The intervention pharmacist will serve as the central source of communication between participants, providers, and (as needed) dispensing pharmacy to coordinate the deprescribing process. The study pharmacists will navigate a shared-decision model between the physicians and participant in order to personalize the selection of appropriate alternatives and switch/titration schedules. Importantly, the pharmacist will supervise the titration and deprescribing plan and communicate with both participants and physicians throughout the study.

OTHER

Usual Care

Those in the usual care group will not have access to the study intervention, but will receive a one-time information packet through the mail reviewing risks of polypharmacy, but no information specific to anticholinergic medications. They will receive clinical care as usually provided by their primary care or specialty care physicians.

Trial Locations (2)

46202

Indiana University Health, Indianapolis

46256

Community Health Network Foundation, Inc., Indianapolis

All Listed Sponsors
collaborator

National Institute on Aging (NIA)

NIH

lead

Indiana University

OTHER