search
Back to results

End-of-Life Health Care Decisions by Patients With Advanced Cancer

Primary Purpose

Neoplasms

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
computer-based decision aid
standard care
Sponsored by
Milton S. Hershey Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Neoplasms focused on measuring advance care planning, living wills, end of life, cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years of age or older
  • able to give informed consent
  • interested in participating in advance care planning
  • able to read and understand English at an 8th grade level (per WRAT-3 screening test)
  • advanced cancer (primary or metastatic), with estimated lifespan < 6 months (as determined by their treating physician)
  • cognitively able to engage in advance care planning (Mini Mental State Exam (MMSE) score >23)
  • absence of moderate or severe depression (BDI-II score <20/63)

Exclusion Criteria:

  • unable to read and understand English at an 8th grade level (per Wide Range Achievement Test (WRAT-3))
  • not cognitively able to engage in advance care planning (Mini Mental State Exam (MMSE) score < 23)
  • moderate or severe depression (BDI-II score >20/63)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    computer-based decision aid

    standard care

    Arm Description

    "Making Your Wishes Known: Planning Your Medical Future"- Offers tailored education, values clarification exercises, and a sophisticated decision aid that translates an individual's goals and preferences into a specific medical plan that can be implemented by a health care team.

    paper/pencil living will form

    Outcomes

    Primary Outcome Measures

    Participant knowledge of advance care planning
    Knowledge of advance care planning will be compared between control and intervention groups, using a true/false and multiple choice questionnaire about advance care planning.

    Secondary Outcome Measures

    Participant decisional conflict
    Assessment of conflict associated with making end-of-life decisions will be assessed with the decisional conflict scale.
    Participant satisfaction with decision
    Assessment of satisfaction with decisions associated with advance care planning will be assessed with the satisfaction with decision scale.
    Participant satisfaction with advance care planning
    Satisfaction with with advance care planning process will be compared between intervention and control group with a satisfaction questionnaire.
    Participant self-determination
    Self determination will be compared between intervention and control group with a self-determination questionnaire.
    Participant anxiety
    Pre and post-intervention anxiety will be compared between intervention and control group with the state trait anxiety instrument.
    Participant hopelessness
    Assessment of pre and post-intervention hopelessness will be compared between intervention and control group using the Beck Hopelessness scale and a measure of hopefulness.
    Physician awareness of patients' health care wishes
    Comparison will be made between intervention and control group regarding whether an advance directive is present in the patient's medical record, and whether the physician is aware of the patient's wishes.
    Physician adherence to patients' health care wishes
    Comparison will be made between intervention and control group regarding whether patients' wishes are followed at the end of life.

    Full Information

    First Posted
    July 30, 2014
    Last Updated
    March 23, 2018
    Sponsor
    Milton S. Hershey Medical Center
    Collaborators
    American Cancer Society, Inc.
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT02265601
    Brief Title
    End-of-Life Health Care Decisions by Patients With Advanced Cancer
    Official Title
    End-of-Life Health Care Decisions by Patients With Advanced Cancer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2008 (undefined)
    Primary Completion Date
    January 2017 (Actual)
    Study Completion Date
    January 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Milton S. Hershey Medical Center
    Collaborators
    American Cancer Society, Inc.

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study is designed to help the investigators understand more about how people plan for their future medical needs, a process known as "advance care planning." The study is under the direction of Michael J. Green, M.D., and Benjamin Levi, M.D. physicians at Penn State Hershey Medical Center. Participation in the project takes place during a single visit to the Medical Center campus. During this one-to-three hour visit, participants complete several questionnaires and use a computer program that produces a printed advance directive that can be shared with their physicians and loved ones. Participants will receive compensation toward travel expenses.
    Detailed Description
    Background: Despite widespread agreement that individuals ought to plan for their medical futures, few people (even seriously ill patients with cancer) actually complete advance directives, fewer yet understand key elements, and even when advance directives do exist, there are often barriers to their being implemented. Objectives: The investigators innovative, multimedia, interactive, computer-based decision aid, "Making Your Wishes Known: Planning Your Medical Future," offers tailored education, values clarification exercises, and a sophisticated decision aid that translates an individual's goals and preferences into a specific medical plan that can be implemented by a health care team. This project aims to evaluate its impact on decision-making and health care received by individuals at the end of life in a randomized clinical trial among a population of patients with advanced cancer who have life expectancies of < 12 months. Specific Aims: Aim 1: To evaluate the impact of a computer-based advance care planning intervention on end-of-life decision-making by cancer patients with estimated life expectancies < 12 months. The investigators hypothesize that, compared to standard care (paper/pencil living will form), use of the computer-based intervention will: H1: Improve individuals' decision-making about end-of-life health care H2: Improve individuals' experience with the process of advance care planning H3: Not increase individuals' hopelessness or anxiety, nor harm the doctor-patient relationship Aim 2: To evaluate the impact of the investigators intervention on end-of-life health care received by cancer patients with estimated life expectancies < 12 months. The investigators hypothesize that, compared to standard care, use of the computer intervention will: H4: Increase physician awareness of individuals' health care wishes H5: Increase physician adherence to individuals' health care wishes Study Design: Randomized, controlled pre-intervention/post-intervention trial comparing a computer-based educational intervention with standard care Cancer Relevance: Patients with advanced cancer face many medical decisions, some of which must be made when the patient cannot speak for him or herself. Helping these individuals to effectively articulate and communicate their wishes, in advance, can help assure that treatment they receive is consistent with their values, goals and wishes. This study aims to test the effectiveness of the investigators' computer-based intervention. If successful, this intervention can help improve the quality of health care received by cancer patients at the end of life.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Neoplasms
    Keywords
    advance care planning, living wills, end of life, cancer

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    InvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    200 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    computer-based decision aid
    Arm Type
    Experimental
    Arm Description
    "Making Your Wishes Known: Planning Your Medical Future"- Offers tailored education, values clarification exercises, and a sophisticated decision aid that translates an individual's goals and preferences into a specific medical plan that can be implemented by a health care team.
    Arm Title
    standard care
    Arm Type
    Active Comparator
    Arm Description
    paper/pencil living will form
    Intervention Type
    Other
    Intervention Name(s)
    computer-based decision aid
    Other Intervention Name(s)
    "Making Your Wishes Known: Planning Your Medical Future"
    Intervention Description
    Offers tailored education, values clarification exercises, and a sophisticated decision aid that translates an individual's goals and preferences into a specific medical plan that can be implemented by a health care team.
    Intervention Type
    Other
    Intervention Name(s)
    standard care
    Intervention Description
    paper/pencil living will form
    Primary Outcome Measure Information:
    Title
    Participant knowledge of advance care planning
    Description
    Knowledge of advance care planning will be compared between control and intervention groups, using a true/false and multiple choice questionnaire about advance care planning.
    Time Frame
    Pre and post-intervention
    Secondary Outcome Measure Information:
    Title
    Participant decisional conflict
    Description
    Assessment of conflict associated with making end-of-life decisions will be assessed with the decisional conflict scale.
    Time Frame
    post-intervention
    Title
    Participant satisfaction with decision
    Description
    Assessment of satisfaction with decisions associated with advance care planning will be assessed with the satisfaction with decision scale.
    Time Frame
    post-intervention
    Title
    Participant satisfaction with advance care planning
    Description
    Satisfaction with with advance care planning process will be compared between intervention and control group with a satisfaction questionnaire.
    Time Frame
    post-intervention
    Title
    Participant self-determination
    Description
    Self determination will be compared between intervention and control group with a self-determination questionnaire.
    Time Frame
    pre and post-intervention
    Title
    Participant anxiety
    Description
    Pre and post-intervention anxiety will be compared between intervention and control group with the state trait anxiety instrument.
    Time Frame
    pre and post-intervention
    Title
    Participant hopelessness
    Description
    Assessment of pre and post-intervention hopelessness will be compared between intervention and control group using the Beck Hopelessness scale and a measure of hopefulness.
    Time Frame
    pre and post-intervention
    Title
    Physician awareness of patients' health care wishes
    Description
    Comparison will be made between intervention and control group regarding whether an advance directive is present in the patient's medical record, and whether the physician is aware of the patient's wishes.
    Time Frame
    post-death chart review
    Title
    Physician adherence to patients' health care wishes
    Description
    Comparison will be made between intervention and control group regarding whether patients' wishes are followed at the end of life.
    Time Frame
    post-death chart review

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: 18 years of age or older able to give informed consent interested in participating in advance care planning able to read and understand English at an 8th grade level (per WRAT-3 screening test) advanced cancer (primary or metastatic), with estimated lifespan < 6 months (as determined by their treating physician) cognitively able to engage in advance care planning (Mini Mental State Exam (MMSE) score >23) absence of moderate or severe depression (BDI-II score <20/63) Exclusion Criteria: unable to read and understand English at an 8th grade level (per Wide Range Achievement Test (WRAT-3)) not cognitively able to engage in advance care planning (Mini Mental State Exam (MMSE) score < 23) moderate or severe depression (BDI-II score >20/63)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michael J. Green, MD, MS
    Organizational Affiliation
    Penn State College of Medicine, Penn State Milton S. Hershey Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    End-of-Life Health Care Decisions by Patients With Advanced Cancer

    We'll reach out to this number within 24 hrs