N/A
N=30
The R4R Advance Care Planning Pilot Study
Advance Care Planning
Bottom Line
View on ClinicalTrials.gov: NCT06129149 ↗Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcome: Primary: Advance Care Planning Values/Beliefs — 24.9; 26.3 Score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Trauma-Informed Care-adapted and Checklist-guided ACP intervention (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Vanderbilt University
- Primary completion
- Dec 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Advance Care Planning Values/Beliefs |
24.9; 26.3 | — |
| PRIMARY Advance Care Planning Processes |
29.2; 43.8 | — |
| PRIMARY Advance Care Planning Actions |
8.6; 12.6 | — |
| PRIMARY Implementation Acceptability |
29 | — |
| PRIMARY Implementation Appropriateness |
24 | — |
| PRIMARY Implementation Feasability |
28 | — |
Summary
Affordable housing residents continue to experience multi-faceted insecurity and advance care planning (ACP) challenges even after obtaining secure housing, resulting in significant inequities in quality of care during times of cognitive incapacity. To promote proactive planning for affordable housing residents, this proposal is for a pilot study to test a novel trauma-informed care adapted advance care planning intervention with the following aims: to test initial efficacy of the intervention on ACP outcomes (Aim 1) and determine resident perceptions of intervention acceptability, appropriateness, and feasibility and perceived implementation barriers and facilitators (Aim 2). These data will support the development of a larger scale study of ACP interventions within a resiliency-based hub model to comprehensively support whole-person care and proactive planning for times of cognitive incapacity.
Eligibility Criteria
Inclusion Criteria
- an adult (18+) residing in an affordable housing unit that does not have a completed advance directive
Exclusion Criteria
- inability to provide informed consent or participate in the intervention due to cognitive, auditory, visual impairment or non-English language barrier
Data sourced from ClinicalTrials.gov (NCT06129149). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.