Advance Care Planning With Formerly Homeless Older Adults Residing in Permanent Supportive Housing

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorUniversity of California, San Francisco

About this trial

The homeless population is aging, with an increasing proportion of individuals over age 50 who experience accelerated aging, high rates of mortality, and a high risk of not having their wishes honored at the end of life. The goal of this randomized control trial (RCT) is to test the effectiveness of adapted evidence-based advance care planning (ACP) interventions for formerly chronically homeless older adults living in permanent supportive housing (PSH).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Formerly chronically homeless adults living in permanent supportive housing

English speaking

Disqualifiers

Non-English Speaking

Screen positive for moderate-to-severe cognitive impairment

Self-report being deaf or blind

Cannot provide informed consent based on the teach back method

Trial design

Design model

Parallel

Treatments tested in this trial

  • Facilitated Group ACP Session

    Behavioral

    Group Facilitators will adhere to the standardized scripts and protocols to engage participants in ACP through group sessions. Participants will view the movie version of the PREPARE program (about how to choose a medical decision maker and how to decide what matters most in life), including a new PSH-specific video. Participants are provided with a workbook to follow along with the movies. They are also provide the PREPARE easy-to-read advance directive legal forms that they can fill out when they are ready. These forms include new PSH-specific content and a PSH-specific cover letter.

  • Facilitated one-on-one ACP visits

    Behavioral

    Facilitator adheres to the scripts and protocols to engage participants in advance care planning through one-on-one ACP sessions. Participants will view the movie version of the PREPARE program (about how to choose a medical decision maker and how to decide what matters most in life), including a new PSH-specific video. Participants are provided with a workbook that they can use to follow along with the movies. They are also provide the PREPARE easy-to-read advance directive legal forms that they can fill out when they are ready. These forms include new PSH-specific content and a PSH-specific cover letter.

Treatment groups

650 Participants
are divided into 2 treatment groups
Group A: Facilitated Group ACP SessionActive comparator 1 intervention
Group B: Facilitated one-on-one ACP visitsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

ACP Engagement Survey

Our primary analyses will compare change in engagement using the 9-item ACP Engagement Survey average 5-point Likert scores from baseline to 3 and 6 months between study arms (groups vs. one-on-one sessions).

Time frame
Baseline, 3 months, and 6 months

Secondary outcomes

1

Individual ACP Behaviors

Secondary outcomes include dichotomous versions of 5 key ACP behaviors (e.g., surrogate designation and AD completion)

Time frame
Baseline, 3 months, and 6 months

Other outcomes

1

Meeting Goals of Care (exploratory)

The field of ACP is evolving, including its recommendations on appropriate and feasible ACP measures. There are no validated self reported or chart abstraction measures for goal concordant care, and there is debate about whether this outcome can be measured effectively. One recommendation is to measure whether the interventions met individuals' needs. Our team will assess if the materials and interventions met a participant's needs for ACP information.

Time frame
Baseline, 3 months, 6 months
2

Adverse Outcomes

In several prior randomized trials of the PREPARE program in other marginalized populations, our team have not detected any adverse outcomes. However, to monitor for trends, our team will screen for the presence of anxiety and depression using the PHQ-4 and will collect open-ended reports of any PSH residents who report feeling uncomfortable.

Time frame
Baseline, 3 months, and 6 months

Sponsors and contacts

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University of California, San Francisco

Lead sponsor

National Institute on Aging (NIA)

Collaborator