Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT03256110 |
Other study ID # |
5R21NR016611 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
January 28, 2019 |
Est. completion date |
July 1, 2021 |
Study information
Verified date |
October 2021 |
Source |
Southcentral Foundation |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
This mixed-methods study is culturally tailoring and evaluating a communication intervention
to increase the frequency and quality of advance care planning with diverse American Indian
and Alaska Native adults with serious, life-limiting illness in primary care at two sites.
Description:
Palliative care is an interdisciplinary field that aims to relieve emotional, spiritual and
physical suffering and improve quality of life in patients with serious, life-limiting
illness and their families. Unfortunately, palliative care is often introduced too late in
the course of care to maximize its potential benefits, in part because healthcare providers
and patients alike lack the knowledge and self-efficacy to initiate conversations about
advance care planning (ACP). ACP is an important component of palliative care in which
patients, families and providers discuss and plan for the patient's desired treatment goals,
including preferences for care and who can make decisions on the patient's behalf if needed.
Integrating ACP into treatment early, before serious, life-limiting illness advances to a
late stage, can improve patient and caregiver quality of life, length of survival, and health
care cost. Primary care is an ideal setting for early integration of ACP, as primary care
providers routinely diagnose and care for patients in the early stage of serious,
life-limiting conditions, such as chronic obstructive pulmonary disease. Alaska Native and
American Indian (AN/AI) people have disproportionately high prevalence of many serious,
life-limiting conditions, including cancer, coronary heart disease, and liver disease. Yet,
AN/AIs use ACP and other palliative care services significantly less than the overall
population. The reasons for this disparity are unclear, and AN/AIs are among the most
underrepresented groups in palliative care studies. Previous research indicates that when
given the opportunity, AIs will engage in ACP, and our preliminary data suggest strong
support among ANs for developing culturally congruent ACP interventions in primary care
settings. The need for timely and effective ACP is growing in AN/AI communities and there is
a pressing need for culturally-congruent, patient-centered palliative care interventions for
AN/AIs as tribal health systems manage rising numbers of AN/AI individuals with serious,
life-limiting illnesses. The aims of this collaborative, community-engaged, clinical study
are to: 1) conduct focus groups with 40 key stakeholders (patients, caregivers, providers,
administrators) in two tribal health systems to tailor an existing ACP communication
intervention for AN/AIs with serious, life-limiting illness; 2) evaluate the cultural
relevance and usability of the tailored ACP communication intervention among 20 AN/AI
patients using cognitive interviews; and 3) compare the impact of the tailored intervention
on frequency of ACP discussions, as well as quality of and satisfaction with ACP
communication between 30 AN/AI patients receiving individualized information to prompt ACP
discussions with providers and 30 AN/AI patients receiving usual care, with information to
prompt a discussion. Implementing effective, appropriate ACP is a high priority at
Southcentral Foundation (SCF) and First Nations Community HealthSource (FNCH), two tribal
health systems serving large, diverse populations of AN/AI people in Alaska and New Mexico.
This study will develop and evaluate a culturally congruent, patient- centered ACP
intervention at these sites and produce evidence for a large, multi-site clinical trial of
the intervention that could improve patient and caregiver outcomes in this diverse population
of more than 5 million Americans.