Skip to content

Development of a Community Engagement Activity for Advance Care Planning

Development of a Community Engagement Activity for Advance Care Planning

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02575417
Acronym
CERC
Enrollment
93
Registered
2015-10-14
Start date
2015-08-31
Completion date
2016-11-30
Last updated
2020-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Disease

Keywords

advance care planning, end-of-life care, health games, Family caregivers, Advance directives

Brief summary

This study will determine the feasibility of using an end-of-life conversation game (called My Gift of Grace) as a community engagement activity series to help caregivers, patients with chronic illness, and/or their families perform advance care planning.

Detailed description

While many patients and caregivers of individuals with chronic illness recognize the importance of advance care planning, many feel uncomfortable initiating end-of-life conversations with loved ones. Few tools exist that effectively engage caregivers and address their particular concerns and needs. The investigators have preliminary data showing that an easily implementable intervention (a conversation game) effectively engages healthy participants in realistic and satisfying ACP conversations. However, the investigators have not yet tested the acceptability or feasibility of using the game in a population of caregivers and/or patients with chronic illness. This pilot project will enable us to engage community-based patients and caregivers to determine if they find the game a satisfying, acceptable, relevant, and effective tool for advance care planning.

Interventions

BEHAVIORALConversation Game

The game consists of 47 question cards that prompt players to identify and articulate their values and beliefs related to dying and end-of-life issues; 20 questions have been selected for this study

Sponsors

Milton S. Hershey Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Participants are eligible to participate if they fall into at least one of the following three groups: 1. CAREGIVER criteria include: 1. are 18 years or older 2. speak and read English 3. 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; 4. are able to sit for about 2.5-3 hours 5. are able to focus on the game for about 1.5-2 hours 6. can complete required survey 7. care recipient is capable of discussing medical issues 8. care recipient has not completed an AD in past 18 months 2. PATIENT criteria include: 1. are 18 years or older 2. speak and read English 3. 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 criteria67) 4. have not completed an advance directive within the past 18 months 5. are able to sit for about 2.5-3 hours 6. are able to focus on the game for about 1.5-2 hours 7. can complete required surveys 3. SURROGATE DECISION MAKERS FOR PATIENTS WITH CHRONIC ILLNESS criteria include: 1. considers themselves a surrogate decision maker for an adult with a chronic illness (defined above) 2. are 18 years or older 3. speak and read English 4. are able to sit for about 2.5-3 hours 5. are able to focus on the game for about 1.5-2 hours 6. can complete required surveys

Exclusion criteria

1. Do not fall into any of the three categories above 2. Have a diagnosis of dementia (by self-report or chart review) 3. Fall into the Surrogate Decision Maker category but the patient cannot also participate in the same study session

Design outcomes

Primary

MeasureTime frameDescription
Change in self-efficacy and readiness to perform advance care planning behaviorsBaseline (before study session) and 12 weeks post-study55-item survey, likert scale ratings

Secondary

MeasureTime frameDescription
Experiences and perceptions of intervention10 minutes after intervention endsFocus-group, open-ended qualitative questions

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026