← Back to all trials
Completed
NCT04270474
Reducing Risk of Dementia Through Deprescribing
Conditions: Dementia, Alzheimer Disease, Late Onset
Sex: All
Ages: 65 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 344
Sponsor: Indiana University
Location: Indiana University Health Indianapolis Indiana
Summary
A cluster-randomized controlled trial (RCT) called "Reducing Risk of Dementia through Deprescribing" (R2D2) to evaluate the impact of a deprescribing intervention on important cognitive and safety outcomes.
Eligibility Criteria
Inclusion Criteria for Participants:
* Age 65 and older;
* At least one office visit to their primary care physician within the previous 12 months;
* Use of a target anticholinergic medication within the last two weeks OR medical record evidence of exposure to target anticholinergic medications at or above a cognitive risk threshold in the prior 12 months
* Able to communicate in English;
* Access to a telephone
Exclusion Criteria for Participants:
* Permanent resident of an extended care facility (nursing home)
* Diagnosis of schizophrenia, bipolar disorder, or schizoaffective disorder defined by International Classification of Diseases (ICD) version 9/10 codes
* Diagnosis of Alzheimer's Disease or Related Dementia as determined by (a), (b), or (c) below:
1. ICD-9/10 codes, or
2. Current use of a medication for Alzheimer's Disease or a Related Dementia, or
3. A pattern of responses to the Functional Activities Questionnaire (FAQ) that indicate dementia (i.e., ≥ 3 FAQ items are scored at "requires assistance," or if ≥ 1 FAQ item is scored at "dependent").
Source: ClinicalTrials.gov (NCT04270474). StuddyBuddy aggregates publicly available trial information.