Actively Recruiting

Phase Not Applicable
Age: 50Years +
All Genders
Healthy Volunteers
ID06239896

Empowering Formerly Homeless Older Adults to Engage in Advance Care Planning in Permanent Supportive Housing: An RCT

Led by University of California, San Francisco · Updated on 2025-11-20

650

Participants Needed

6

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of California, San Francisco

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating adapted advance care planning (ACP) programs for formerly chronically homeless older adults living in permanent supportive housing (PSH). This study aims to address the low rates of ACP in this aging population, which faces accelerated aging, high mortality, and risk of having their end-of-life wishes unmet. The trial focuses on comparing different ways to deliver ACP and improving engagement among residents of PSH. The study tests two ways of delivering the PREPARE-PSH program, an evidence-based, easy-to-use online ACP program with videos and easy-to-read advance directive forms tailored for the PSH setting. Participants are randomly assigned by site to either a one-time 90-minute facilitated group session or a one-on-one ACP visit, both including viewing videos about choosing a medical decision maker and deciding what matters most in life. The program also provides workbooks and legal forms with PSH-specific content. Participants will be followed over time with surveys measuring their engagement in advance care planning at the start, 3 months, and 6 months after the sessions. Researchers will also conduct interviews and focus groups to understand factors influencing engagement and sustainability of the program. The total participation includes attending the session and completing follow-up assessments to evaluate ACP behaviors and preferences.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Formerly chronically homeless adults living in permanent supportive housing
  • English speaking
  • Age 50 years or older
Not Eligible

You will not qualify if you...

  • Non-English speaking
  • Moderate-to-severe cognitive impairment
  • Self-report being deaf or blind
  • Unable to provide informed consent based on the teach back method

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Single session

Participants take part in a one-time 90-minute advance care planning (ACP) session either in a facilitated group or one-on-one setting. During this session, they view the PREPARE program videos and receive easy-to-read advance directive forms tailored for permanent supportive housing residents.

1 visit (in-person)

Long-term Monitoring

Duration - 6 months

Participants complete surveys and assessments of their ACP engagement and individual ACP behaviors at baseline, 3 months, and 6 months after the ACP session to monitor ongoing outcomes.

3 visits (at baseline, 3 months, and 6 months)

Trial Site Locations

Total: 6 locations

1

Abode Services

Fremont, California, United States, 94538

Actively Recruiting

2

Lifelong Medical Care

Oakland, California, United States, 94612

Actively Recruiting

3

Mercy Housing

San Francisco, California, United States, 94102

Actively Recruiting

4

Delivering Innovation in Supportive Housing (DISH)

San Francisco, California, United States, 94103

Actively Recruiting

5

Episcopal Community Services

San Francisco, California, United States, 94103

Actively Recruiting

6

HomeRise

San Francisco, California, United States, 94104

Actively Recruiting

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Research Team

L

Layan Kaileh, MSW

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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