Improving PCP Advance Care Planning for People With ADRD
Launched by UNIVERSITY OF PITTSBURGH · Aug 19, 2024
Trial Information
Current as of October 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring a new tool called the Dementia Advance Care Planning (AD ACP) Toolkit to help improve conversations about care goals for people living with dementia. The study will compare how well this toolkit works alongside standard care in helping patients and their primary care teams discuss important topics related to their health and future care plans. Over 18 months, the researchers will look at how often these discussions happen and how effective they are, as well as track things like identifying caregivers and completing advance care planning orders.
To participate, people living with dementia need to be 65 years or older and have a diagnosis of Alzheimer’s disease or related disorders. They must also have seen their primary care doctor in the past 18 months. Primary care team members involved must be doctors or advanced practice providers who regularly care for older adults at specific clinics. If eligible, participants can expect to engage in conversations about their health, preferences, and care planning, which can help ensure their wishes are respected as their condition progresses. This study aims to create better care experiences for patients living with dementia and their families.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- Primary care team member (PCTM) eligibility:
- • Must be an MD/APP, employed at a primary care clinic within UNC HEALTH clinics with ≥60 PLwD encounters per year, who sees older adult patients, along with their associated nurses and social workers.
- • Eligibility for training with AD ACP Toolkit will include the above and the provision of care at an intervention clinic.
- • For Aim 3, only the trained intervention site primary care team members will be eligible for the implementation surveys or the interviews.
- PLwD eligibility:
- • Must be a PLwD age 65 years or older seen by either the intervention or control sites' primary care teams' MD/APP in the 18-month intervention window for Aim 1.
- • PLwD will be eligible only after we confirm the presence of the AD/ADRD diagnosis.
- • All PLwD with a ≥50% 5-year all-cause mortality risk seen by the PCTM MD/APP over the 18-month intervention period will be eligible for the healthcare utilization analyses in Aim 2.
- Exclusion Criteria:
- Primary care team member exclusion criteria:
- • We will exclude primary care team members who do not care for older adults (e.g. pediatricians or lactation nurses), are employed at geriatric specialty or dementia specialty clinics, or are without a primary care panel (e.g., only urgent care).
- PLwD exclusion criteria:
- • Patients will be excluded if they have not been seen in the past 18 months by their primary care team, or if they do not have a diagnosis of ADRD.
About University Of Pittsburgh
The University of Pittsburgh is a leading research institution known for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a robust infrastructure for research and a multidisciplinary approach, the university fosters collaboration among experts in various fields, facilitating the development of novel therapies and interventions. Its clinical trial programs emphasize ethical standards, patient safety, and the integration of cutting-edge technology, making the University of Pittsburgh a pivotal contributor to the landscape of clinical research and a trusted partner in the pursuit of health advancements.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chapel Hill, North Carolina, United States
Patients applied
Trial Officials
Christine E. Kistler, MD, MASc
Principal Investigator
University of Pittsburgh, Department of Medicine, Division of Geriatric Medicine
Laura C. Hanson, MD, MPH
Principal Investigator
University of North Carolina, Chapel Hill
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported