Deprescribing Potentially Inappropriate Medications in the Emergency Department for Persons Living With Dementia
Completed · Not applicable
Conditions studied: Dementia
In brief
Aim 1: To demonstrate the feasibility by determining proportion of completed medication reconciliation, Central Nervous System active Potentially Inappropriate Medication (CNS PIM) use among patients with Alzheimer's Disease and Related Dementias (ADRD) and Mild Cognitive Impairment (MCI) in the emergency department (ED), and communication between ED clinical pharmacists and outpatient prescribers. Aim 2: To demonstrate the feasibility of collecting the primary and secondary outcomes for a subsequent study. The future primary outcome will be reduction in CNS PIMs 90 days after an ED visit. Secondary outcomes will include outpatient follow-up, repeat ED visits, and hospitalizations during the 90 days following an ED visit. Aim 3: To demonstrate the acceptability of the PRIDE intervention to outpatient clinicians using the Acceptability of Intervention Measure and qualitative analysis of responses.
Key facts
- Study ID
- NCT06273917
- Run by
- National Institute on Aging (NIA)
- People needed
- 300
- Starts
- 2024-07-09
- Expected to finish
- 2025-10-31
- Last updated by the study team
- 2026-07-01
Who can join
Age: 18 and older, up to 120. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Community dwelling
- 18 years of age or older
- History of dementia or mild cognitive impairment in the problem list in the NM EHR. A history of mild cognitive impairment will be identified using the ICD-10 code G31.84 (mild cognitive impairment) or ICD-10 codes suggestive of ADRD as described in the Bynum-standard algorithm: F01.50-F01.51 (vascular dementia), F02.80-F02.81 (dementia), F03.90-F03.91 (unspecified dementia), F04 (amnestic disorder), G30.0/30.1/30.8/G30.9 (Alzheimer's disease), G31.01 (Pick's disease), G31.09 (frontotemporal dementia), G31.83 (dementia with Lewy bodies), G31.1 (senile degeneration), G31.2 (degeneration of nervous system), R41.81 (age-related cognitive decline).
- Able to participate in medication reconciliation as determined by the pharmacist per usual care OR a care partner with knowledge of the patient's current medications is present in the ED or is available by phone.
- Has had prior outpatient care performed at Northwestern Medicine location(s)
- Arrives to the emergency department between 7am and 7pm, Monday-Friday
You may not qualify if…
- Emergency Severity Index (ESI) of 1 (critical)
- ICU consult placed in the ED
- Reside in nursing facility or assisted living facility
Where it is running
- Northwestern Memorial Hospital — Chicago, Illinois, United States
- Northwestern Medicine Lake Forest Hospital — Lake Forest, Illinois, United States
- Northwestern Medicine Palos Hospital — Palos Heights, Illinois, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.