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N/A N=759 Randomized Health Services Research

Integrated Multidisciplinary Patient and Family Advance Care Planning Trial

Advance Care Planning

Enrolled (actual)
759
Serious AEs
0.0%
Results posted
Aug 2021
Primary outcome: Primary: Number of Patient's Documented Advance Care Planning Discussion- Nurse Navigator — 134; 0 Discussions

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Nurse Navigator Pathway (Behavioral); Usual Care (Behavioral)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
Wake Forest University Health Sciences
Primary completion
Dec 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patient's Documented Advance Care Planning Discussion- Nurse Navigator
134; 0
PRIMARY
Number of Patient's Documented Advance Care Planning Discussions - Provider
160; 14
PRIMARY
Quality of Advance Care Planning Discussion - Nurse Navigator
PRIMARY
Quality of Advance Care Planning Discussion - Provider
PRIMARY
Quality of Advance Care Planning Discussion From the Patient's Perspective
10.2; 7.9
SECONDARY
Advance Care Planning Billing Code Usage
96; 5
SECONDARY
Number of Designated Surrogate Decision Makers
241; 132
SECONDARY
Advance Directive Completion
92; 38

Summary

The purpose of this study is to compare ways to engage sick patients and their family members in Advance Care Planning (ACP) discussions. Two pathways will be tested, discussions using a Nurse Navigator led pathway versus usual care.

Eligibility Criteria

Inclusion Criteria

  • Aged 65 or older patient within the Wake Forest/Cornerstone ACO
  • Have seen their primary care provider within the Wake Forest/Cornerstone network in the past 12 months
  • English speaking
  • No documented Advance Directive in the EHR
  • Impairments in either physical function, cognition, and/or frailty

Exclusion Criteria

  • No available proxy (e.g. in setting of cognitive impairment)
  • Severe/advanced dementia
  • Moderate to severe hearing loss
  • Non-English speaking
  • No phone number available for patient
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03609658). 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.

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