Clinical Trial Details
— Status: Enrolling by invitation
Administrative data
NCT number |
NCT05324878 |
Other study ID # |
NCR213481 |
Secondary ID |
DI-2020C2-20362 |
Status |
Enrolling by invitation |
Phase |
|
First received |
|
Last updated |
|
Start date |
September 1, 2021 |
Est. completion date |
July 1, 2024 |
Study information
Verified date |
June 2023 |
Source |
George Washington University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
The PCORI HIGHway project name embodies its goal: the way to "Honor Individuals Goals and
Hopes". HIGHway trains and supports dialysis center social workers and nurses to communicate
with their patients about their hopes and goals for their future care plans. This process,
known as advance care planning (ACP), helps relieve patient concerns about the future, lays
the foundation for better goal-concordant care at the end of life, and fosters deeper
connection between patient and the dialysis care team. The HIGHway project will provide
training and ongoing coaching to social workers and other change team members at 50-60
dialysis centers throughout the US. The goal is to integrate advance care planning
conversations between dialysis patients and their health care team into the ongoing workflow
of dialysis centers. The project is funded by the Patient Centered Outcomes Research
Institute (PCORI), a non-profit organization chartered by Congress to fund projects to
promote patient-centered care.
Description:
OBJECTIVES Primary Objective: The HIGHWay project trains dialysis center teams to conduct ACP
conversations with patients with kidney failure. Emphasis is on training and supporting the
dialysis center social worker to be the team leader for ACP, in collaboration with the
nephrologist and other clinicians.
Aims:
1. Implement the HIGHway intervention with a project team consisting of a social worker,
nephrologist and nurse at 50 clinics, and train them to conduct ACP using best
practices.
2. Assist social workers/nurses to implement ACP into their regular workflow with personal
coaching, webinars and multimedia teaching materials.
3. Use a dedicated web-based application software to guide social workers/nurses on the ACP
process of patients in dialysis centers and provide resources for holding ACP
conversations.
4. Provide ongoing coaching through monthly teleconferences to bolster social worker/nurse
skills through case discussion and mentoring.
5. Develop a long-term implementation and scale-up plan for training social workers/nurses
in ACP in different dialysis centers in conjunction with the Coalition for Supportive
Care of Kidney Patients, Forum of ESRD Networks, the National Council of Nephrology
Social Workers, the National Renal Administrators Association, and dialysis
organizations.
RELEVANT BACKGROUND Patient-centered care problem addressed: Patients on dialysis want to
discuss their preferences for treatment at the end of life, but few do so, and most
nephrologists are reluctant or feel unprepared to lead such discussions. Effective tools are
critically needed to elicit such preferences since over 50,000 Americans die of kidney
disease annually, more than from breast or prostate cancer. For dialysis patients with
significant co-morbidities, risk of death within a year of starting dialysis is stark. Of
those who had 4 or more comorbidities, 26% died within 30 days of dialysis initiation, and
60% died within a year. These patients have higher - and often unwanted - intensity of care
at end of life; in a four-year study of the United States Renal Data System, 49% of elderly
long-term hemodialysis (HD) patients spent time in an intensive care unit in their final
month of life, compared with 24% of cancer patients. Meaningful end-of-life conversations can
change these outcomes and are associated with increased hospice referral, less aggressive and
expensive medical treatment, and higher levels of family satisfaction. Yet less than 10% of
end-stage renal disease (ESRD) patients report having a conversation about any end-of-life
issues with their nephrologist in the previous year, although 90% said such conversations
were important. Few patients with ESRD engage in ACP, and the vast majority lack a written
advance directive or surrogate decision maker, leaving them unprepared to provide guidance in
medical decisions in a crisis.
A prior study funded by PCORI developed and tested an intervention to enable more advance
care planning to take place in dialysis centers. The Shared Decision Making - Renal
Supportive Care (SDM-RSC) study tested a multi-modal patient-centered intervention to improve
advance care planning for dialysis patients. Through qualitative interviews with advisory
boards comprised of patients and stakeholders, SDM-RSC investigators designed an intervention
that focused on goals of care conversations between patients and family members with the
nephrologist and social worker. The SDM-RSC intervention targeted deficiencies in
communication, estimating prognosis, and transition planning for seriously ill dialysis
patients. The intervention showed capacity to increase substantially completion of advance
directives and medical orders (Medical Orders for Life-Sustaining Treatment [MOLST]/Physician
Orders for Life-Sustaining Treatment [POLST]) associated with improved patient-level
end-of-life (EOL) outcomes. Among study participants, the advance directive completion rate
and understanding of advance directives were substantially higher than in usual care; 75% of
participants named and documented a healthcare proxy and 63% had medical orders (MOLST or
POLST) (in comparison to 49% with advance directives and 3% with medical orders in usual
care). The average duration time for an ACP conversation was about 45 minutes. Overall
clinic-level hospice usage using retrospective data did not vary significantly between the
pre- and post-intervention 6-month periods with an observed average rate of 25% which is
close to the 2015 national average of 26% among all ESRD Medicare decedents. However, among
deceased study participants who engaged in a Shared Decision Making and Renal Supportive Care
(SDMRSC) meeting, 48% voluntarily withdrew from dialysis prior to death and 39% received
hospice services (compared to the overall rate in these dialysis centers of 24.8%).
There were high levels of family satisfaction (FAMCARE results) and no adverse intervention
effects on patients or surrogates on measures of depression and health-related quality of
life. The stakeholder advisory council and the respondents on post-intervention interviews
recommended the following: a) streamlining and focusing the social worker training; b)
offering the advance care planning conversation to all dialysis patients, not just those who
were seriously ill, c) broadening the population to include home dialysis patients; and d)
offering a telehealth option for conducting the discussions.
The current study builds on the SDM-RSC results to implement the revised intervention in a
broader population with a larger number of participating dialysis centers.