Evaluation of an Advance Care Planning Activity: Feasibility Testing for a Randomized Controlled Trial

March 21, 2017 updated by: Lauren Van Scoy
The overarching goal of this project is to facilitate engagement of individuals in effective advance care planning (ACP). Our specific objective is to conduct a randomized, controlled trial to determine whether playing a structured conversation game will increase the likelihood that participants will complete advance directives and perform other ACP behaviors compared to those who are provided with only standard ACP educational materials.

Study Overview

Detailed Description

Our central hypothesis is that having ACP conversations in a non-threatening and enjoyable game format will stimulate participants to engage in additional ACP behaviors including completion of ADs. We will use the ACP Engagement Survey to measure readiness to perform ACP, which includes measures of the "stage of change" for performing ACP behaviors.

The proposed study has two specific aims:

Aim 1. To determine whether individuals who play a conversation game are more likely to subsequently complete an online AD (called 'Making Your Wishes Known'; MYWK) compared to individuals who receive standard information about ACP. Our hypothesis is that playing a conversation game will result in a higher AD completion rate (compared to control) in the three months following the intervention.

Aim 2. To identify which participant and/or conversation-related factors influence movement along the stages of change continuum with respect to ACP behaviors (discussing end-of-life wishes with families or clinicians and then completing ADs). Our hypotheses are that: H1) the game intervention will lead to higher quality conversations than the control; and H2) participants whose conversations consist of high-quality ACP discussions will be more likely to progress toward enacting ACP behaviors (as measured by the ACP Engagement Survey score) than those participants whose conversations consist of low-quality discussions.

Study Type

Interventional

Enrollment (Actual)

34

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Participants are eligible to participate if they fall into at least one of the following three groups:

  • Group 1) CAREGIVERS:

    • are 18 years or older
    • speak and read English
    • have been an unpaid caregiver for an adult over the age of 18 in the last 12 months. Being an unpaid caregiver may include helping with personal needs or household chores, managing a person's finances, arranging for outside services, or visiting regularly to see how they are doing. This person need not live with participants in order for them to identify as caregivers;
    • are able to sit for about 2.5-3 hours
    • are able to focus on the game for about 1.5-2 hours
    • can complete required survey
    • care recipient is capable of discussing medical issues
    • care recipient has not completed an AD in past 18 months
  • Group 2) PATIENTS WITH CHRONIC ILLNESS; criteria include:

    • are 18 years or older
    • speak and read English
    • have at least one chronic illness (cancer, chronic pulmonary disease, coronary artery disease, congestive heart failure, peripheral vascular disease, severe chronic liver disease, diabetes with end organ damage, renal failure-defined using Iezonnis' ICD-9 criteria*)
    • have not completed an advance directive within the past 18 months
    • are able to sit for about 2.5-3 hours
    • are able to focus on the game for about 1.5-2 hours
    • can complete required surveys
  • Group 3) SURROGATE DECISION MAKERS FOR PATIENTS WITH CHRONIC ILLNESS criteria include:

    • considers themselves a surrogate decision maker for an adult with a chronic illness (defined by Iezonni's ICD-9 chronic illness categories*)
    • are 18 years or older
    • speak and read English
    • are able to sit for about 2.5-3 hours
    • are able to focus on the game for about 1.5-2 hours
    • can complete required surveys
  • Iezonni's ICD-9 'chronic illness' definition contains codes within any of the following categories:

    1. malignant cancer/leukemia
    2. chronic pulmonary disease
    3. coronary artery disease
    4. congestive heart failure
    5. peripheral vascular disease
    6. severe chronic liver disease
    7. diabetes with end-organ damage
    8. renal failure.

Exclusion Criteria:

  • Do not fall into one of the above 3 categories
  • Are <18 years of age
  • Non-English speaking
  • Cognitively impaired by self-report or score less than 21 on the MoCA screening tool
  • Do not have a chronic illness (lacking one of the diseases from Iezonni's ICD-9 codes in chronic illness categories, described above)
  • Have completed an advance directive within the last 18 months
  • Do not provide informed consent or unable to provide informed consent
  • Carry a diagnosis of dementia
  • Unable to complete a 3 hour study session in one sitting (by self-report)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Play 'My Gift of Grace,' a conversation card game for 4-6 players (the game consists of 20 question cards that prompt players to identify and articulate their values and beliefs related to dying and end-of-life issues); all game sessions will be audio recorded and transcribed.
Active Comparator: Control
Review and discuss a brochure on ACP called "Advance Care Planning: Tips from the National Institute of Aging". Discussion will be prompted by the researcher asking participants to discuss the information they've just read with the group. However, there will not be a formal structure to this discussion.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Completion of an online advance directive
Time Frame: 3 months
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Advance Care Planning Engagement Survey
Time Frame: 3 months
This survey includes information about stage of readiness to perform advance care planning, self-efficacy, and other measures of behavioral change
3 months
Advance Care Planning Behaviors
Time Frame: 3 months
Open-ended interviews will ascertain additional advance care planning behaviors performed
3 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Satisfaction with advance care planning questionnaire
Time Frame: 30 minutes after intervention
8-item questionnaire on a 7-point likert scale
30 minutes after intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2016

Primary Completion (Actual)

June 1, 2016

Study Completion (Actual)

September 1, 2016

Study Registration Dates

First Submitted

November 30, 2015

First Submitted That Met QC Criteria

December 1, 2015

First Posted (Estimate)

December 2, 2015

Study Record Updates

Last Update Posted (Actual)

March 22, 2017

Last Update Submitted That Met QC Criteria

March 21, 2017

Last Verified

March 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • STUDY00002634

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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