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Clinical Trials/NCT03141242
NCT03141242
Completed
Not Applicable

Refining an Advance Care Planning Group Visit Intervention - A Novel Intervention to Engage Older Adults in Advance Care Planning.

University of Colorado, Denver1 site in 1 country110 target enrollmentAugust 22, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Advance Care Planning
Sponsor
University of Colorado, Denver
Enrollment
110
Locations
1
Primary Endpoint
Presence of Medical Decision-maker Documentation in the EHR
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The main goal of the ENACT (ENgaging in Advance Care planning Talks) Group Visit intervention is to integrate a patient-centered advance care planning process into primary care, ultimately helping patients to receive medical care that is aligned with their values. The ENACT Group Visit intervention involves two group discussions about advance care planning with 8-10 patients who meet for 2-hour sessions, one month apart, facilitated by a geriatrician and a social worker. This study will compare the ENACT Group Visit intervention to mailed advance care planning materials.

Detailed Description

This pilot feasibility randomized controlled study will determine the feasibility, acceptability and preliminary efficacy of the ENACT Group Visit intervention compared to a comparison arm. The ENACT Group Visit intervention aims to engage patients in an interactive discussion of key ACP concepts and support patient-initiated ACP actions (i.e. choosing decision-maker(s), deciding on preferences during serious illness, discussing preferences with decision-makers and healthcare providers, and documenting advance directives). The group visits involve two 2-hour sessions, one month apart, facilitated by a geriatrician and a social worker. The ENACT Group Visit is based on an intervention manual that guides the structure, facilitator considerations, session format, and documentation and billing details. The discussions include sharing experiences related to ACP, considering values related to serious illness, choosing a surrogate decision-maker(s), flexibility in decision making, and having conversations with decision-makers and healthcare providers. The facilitators support an interactive discussion that promotes opportunities for patients to learn from others' experiences.

Registry
clinicaltrials.gov
Start Date
August 22, 2017
End Date
May 25, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 50 or older
  • Receive primary care through UCHealth, Colorado, USA.

Exclusion Criteria

  • Severe cognitive impairment, known diagnoses of dementia
  • Severe hearing loss or deafness

Outcomes

Primary Outcomes

Presence of Medical Decision-maker Documentation in the EHR

Time Frame: 0, 6 months

An MDPOA form is in electronic medical chart or an orally appointed decision maker

Presence of Advance Directive in the EHR

Time Frame: 0 and 6 months

Presence of any advance directive document in the EHR (e.g., MDPOA, living will, Colorado MOST form)

Secondary Outcomes

  • Change in Readiness to Engage in ACP (ACP Engagement Score)(0, 6 months)
  • Change in Readiness to Discuss Values and Care Preferences With Surrogate Decision Maker(0, 6 months)
  • Change in Readiness to Chose a Surrogate Decision Maker(0, 6 months)
  • Readiness to Sign Official Papers About Medical Care(0 and 6 months)
  • Readiness to Talk to Patient's Physician About Future Medical Care(0 and 6 months)
  • Change in Advance Directive in Medical Record(0, 3, 6, 12 months)

Study Sites (1)

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