Patient Priorities Care Among Persons Living With Mild Cognitive Impairment and Dementia
Completed · Not applicable
Conditions studied: Dementia, Mild Cognitive Impairment
In brief
The goal of this pragmatic, embedded clinical trial is to analyze the implementation of Patient Priorities Care in primary care and geriatrics clinics with patients living with dementia or mild cognitive impairment. This study aims are: * demonstrate the feasibility of using the electronic health record to identify a diverse cohort of eligible patients who will engage in a Patient Priorities Care conversation with a trained facilitator. * demonstrate feasibility of pragmatically assessing clinical outcomes using the electronic health record, including a) number of days at home, b) total medications, and c) new referrals to specialist physicians. * examine key feasibility measures across racial, ethnic, and socioeconomic subgroups. Participants will receive a packet of information about Patient Priorities Care from their primary care clinic, in advance of their next upcoming clinic appointment. Individuals who receive a packet will have the opportunity to engage in a conversation about what matters most to them and what their priorities are, with trained facilitators at the clinic.
Key facts
- Study ID
- NCT06001775
- Run by
- Indiana University
- People needed
- 178
- Starts
- 2023-08-31
- Expected to finish
- 2025-02-15
- Last updated by the study team
- 2026-04-02
Who can join
Age: 40 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient Inclusion Criteria
- Patients must meet all of the following criteria to participate in this study:
- 40 years or older
- English-speaking at both Indiana sites or English and/or Spanish speaking at the University of Texas site
- Receiving care with a participating physician
- Has a scheduled outpatient care visit within 1-2 months (60 days)
- Individual has a diagnosis of MCI or dementia
- Definition: To identify individuals with dementia and MCI, we will use two or more instances of use of an ICD-10 code for either diagnosis in the EHR within 24 months. Typically, we would include instances of these billing codes within a year of each other but, due to the COVID-19 pandemic, recognize that there may be less frequent clinical visits and less robust billing. Diagnostic codes include:
- F01.50, F01.51, F02.80, F02.81, F03.90, G30.0, G30.1, G30.8, G30.9, G31.01, G31.09, G31.1, G31.2, F41.81, G31.84 and F03.91.
- Care Partner Inclusion Criteria
- Care partners must meet all of the following criteria to participate in the study:
- 18 years or older
- English-speaking at both Indiana sites or English and/or Spanish speaking at the University of Texas site
- A note about inclusion of care partners: Clinician determination of a patient's capacity to participate in a visit independently is part of a pragmatic approach. This means that clinic staff will determine when a care partner is needed. Generally, we act under the assumption that patients who require a care partner will have already included them in previous visits and/or provider communications (and we anticipate that this will be documented in the EHR), whereas patients who attend clinic visits independently and have no documentation indicating the involvement of a care partner in their medical decisions, or a need for one, will be determined to have the capacity to also participate in a PPC visit.
You may not qualify if…
- Participants who meet any of the following criteria will be excluded from the study:
- Is not community-dwelling- e.g. lives in a nursing home
- Is enrolled in hospice
- Individuals who decline to receive the PPC intervention (i.e. decline to have the PPC conversation) will be excluded from the study.
- Note that declining to receive the PPC intervention will in no way impact the care that patients receive now or in the future.
Where it is running
- Eskenazi Health — Indianapolis, Indiana, United States
- Indiana University Health Connected Care — Indianapolis, Indiana, United States
- University of Texas Health- Houston — Houston, Texas, United States
Full record on ClinicalTrials.gov
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