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Clinical Trials/NCT06347172
NCT06347172
Completed
Not Applicable

Deprescribing in Patients Living With Dementia With Caregiver and Provider Nudges

Brigham and Women's Hospital1 site in 1 country250 target enrollmentAugust 1, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alzheimer Disease
Sponsor
Brigham and Women's Hospital
Enrollment
250
Locations
1
Primary Endpoint
Composite of the percentage of eligible PCPs or their PLWD/care partners who view or click on information
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

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.

Detailed Description

The PCP nudge will consist of: a 'pre-commitment' EHR nudge triggered when a PCP opens a patient encounter (i.e., prompt to first have a discussion and then later deprescribe) and a brief message within the in-basket prior to upcoming visits including information about their patient. The patient living with dementia (PLWD)/care partner nudge will include an electronic message delivered prior to upcoming visits (in their primary language recorded in the EHR) that includes a recommendation for the PLWD (and care partner, if available) to discuss medications with the PCP at the visit.

Registry
clinicaltrials.gov
Start Date
August 1, 2024
End Date
December 15, 2025
Last Updated
4 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Julie Lauffenburger

Associate Professor

Brigham and Women's Hospital

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Composite of the percentage of eligible PCPs or their PLWD/care partners who view or click on information

Time Frame: On or before the primary care provider visit

This will be the primary progression criteria for the study and measured and evaluated separately by patient and provider.

Secondary Outcomes

  • Number of nudges that fire as intended: Fidelity(On the primary care provider visit)
  • Discontinuation or prescribed reduction in medication(Within 60 days after the primary care provider visit)

Study Sites (1)

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