N/A
N=672
Patient-centered and Efficacious Advance Care Planning in Cancer: the PEACe Comparative Effectiveness Trial
Cancer · Advance Care Planning
Bottom Line
View on ClinicalTrials.gov: NCT03824158 ↗Enrolled (actual)
672
Serious AEs
0.0%
Results posted
Jan 2025
Primary outcome: Primary: Advance Care Planning Engagement — 4.08; 4.34 score on a scale — p=0.0014
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Facilitated advance care planning (in-person or telephonic) (Behavioral); Web-based advance care planning (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Pittsburgh
- Primary completion
- Jan 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Advance Care Planning Engagement |
4.08; 4.34 | 0.0014 sig |
| SECONDARY Number of Participants Who Have Had Advance Care Planning Discussions With Caregivers |
117; 120 | 0.76 |
| SECONDARY Number of Participants Who Have Had Advance Care Planning Discussions With Physicians |
54; 67 | 0.13 |
| SECONDARY Number of Participants Who Have Completed an Advance Directive |
80; 101 | 0.008 sig |
| SECONDARY Documented Care Goals |
4; 18; 1; 8; 29; 31 | 0.002 sig |
| SECONDARY Caregiver Depression Symptoms |
5.87; 5.34 | 0.50 |
| SECONDARY Caregiver Anxiety Symptoms |
6.72; 6.56 | 0.84 |
| SECONDARY Receipt of Goal-concordant End-of-life Care - Patient Wishes Followed |
37; 46; 11; 2; 1; 0 | 0.01 sig |
| SECONDARY Receipt of Goal-concordant End-of-life Care - Place of Death |
34; 37 | 0.83 |
| SECONDARY Quality of End-of-life Care |
5.62; 5.69; 5.51; 5.45; 7.67; 7.7 | 0.32 |
| SECONDARY Caregiver Post-traumatic Stress Symptoms |
1.15; 0.96; 1.99; 1.48; 1.06; 0.74 | 0.01 sig |
| SECONDARY Caregiver Depression Symptoms |
5.87; 5.34 | 0.50 |
| SECONDARY Caregiver Anxiety Symptoms |
6.72; 6.56 | 0.84 |
Summary
The overall goal of this study is to identify the most effective and efficient advance care planning (ACP) strategy for patients with advanced cancer.
The specific aims are to:
Aim 1. Compare the effectiveness of in-person, facilitated ACP versus web-based ACP on patient and family caregiver outcomes.
Aim 2. Assess implementation costs and the effects of in-person, facilitated ACP and web-based ACP on healthcare utilization at end of life.
Aim 3. Identify contexts and mechanisms that influence the effectiveness of in-person, facilitated ACP versus web-based ACP.
Eligibility Criteria
Patient Inclusion Criteria:
- 18 years of age or older
- Solid tumor
- The oncologist "would not be surprised" if the patient died within the next year
- Eastern Cooperative Oncology Group performance status (ECOG PS) of 0, 1, or 2
- Planning to receive ongoing care at a participating oncology clinic
- Willing to participate in either a web-based or facilitated program
Patient Exclusion Criteria:
- Does not speak English
- Inability to consent, using a validated teach-back method
- Hematologic malignancy
- No phone for additional study contacts and follow-up interviews
- Unable to participate in advance care planning, as assessed by clinician
- Unable to complete the baseline interview
Patients will be able to identify and enroll a caregiver, designated by the patient as the primary family member or friend involved in their care and best able to participate in the study.
Caregiver Inclusion criteria:
- 18 years of age or older
- Family member or friend of an eligible patient
- Primary person involved in patient's care and best able to participate in the study, as assessed by patient
Caregiver Exclusion criteria:
- Does not speak English
- No phone for additional study contacts and follow-up interviews
- Unable to complete the baseline interview
Data sourced from ClinicalTrials.gov (NCT03824158). 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.