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Deprescribing in Patients Living With Dementia With Caregiver and Provider Nudges

CompletedNA

Sponsor: Brigham and Women's Hospital

Conditions: Alzheimer Disease, Mild Cognitive Impairment, Dementia

Interventions: Nudge Intervention

Countries: United States

The objectives of this study are to demonstrate the feasibility of implementing a deprescribing nudge intervention using pragmatic methods, confirm that outcomes can be feasibly measured and evaluated at scale in a subsequent embedded pragmatic clinical trial (ePCT), and explore representativeness of persons living with dementia and care partners identified.

Eligibility overview

Sex: ALL

Age: 65 Years to —

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria

Primary care providers will be the primary unit of identification and randomization.

Primary care providers inclusion criteria:

* Providers within Brigham and Women's Hospital primary care practices
* Having prescribed at least one of the high-risk medications of interest

Eligible patients will be identified through this providers within the health care system.

Patient inclusion criteria:

* At least 65 years of age
* Prescribed at least 90 pills of one of the high-risk medications of interest in the last 180 days in the EHR system, which most guidelines consider chronic use, and have a diagnosis of dementia in the EHR.

Locations (1)

Boston, Massachusetts, United States