A Study to Tailor Advance Directives

Sponsor
University of Chicago (Other)
Overall Status
Completed
CT.gov ID
NCT00121004
Collaborator
(none)
100
1
2
49.1

Study Details

Study Description

Brief Summary

In this study, hospitalized patients will first be surveyed regarding their interest in a traditional advanced directive (AD) and then in a modified AD.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Advance Directive Selection

Detailed Description

The purpose of this study is to assess whether patients will execute an advance directive which offers a limited trial of life-sustaining therapy in non-terminal illness, declines life-sustaining therapy or artificial nutrition in advanced dementia, or declines life-sustaining therapy in general. Advance directives (ADs) as currently drafted have been questioned since they have not had much effect on end-of-life care. However, the reason for the lack of success may be simply that they rarely apply. Traditional ADs, which are limited to terminal illness or persistent vegetative states, are difficult to apply to the more common cases of critical illness in the setting of potentially reversible disease and advanced dementia, which are often not recognized as terminal. In addition, terminal ADs are drafted too narrowly for patients who do not wish for life-sustaining therapy regardless of condition.

Patients may execute either AD at the conclusion of the survey. This research has the potential to demonstrate widely reproducible methods on which more precise advance planning can be based and thereby improve end-of-life care.

Study Design

Study Type:
Observational
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Study to Tailor Advance Directives
Study Start Date :
Jul 1, 2005
Actual Primary Completion Date :
Sep 1, 2005
Actual Study Completion Date :
Sep 1, 2005

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Hospitalized patients admitted to the general medical service at the University of Chicago

    • Previously enrolled in a study of hospitalized general medicine patients at the University of Chicago

    Exclusion Criteria:
    • Patients who score less than 17 out of 30 on the Folstein Mini-Mental Status Examination or who have a proxy decision-maker

    • Patients who are medically unstable based on two or more abnormal vital signs

    • Patients who face a possible new diagnosis of cancer

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The University of Chicago Chicago Illinois United States 60637

    Sponsors and Collaborators

    • University of Chicago

    Investigators

    • Principal Investigator: Elmer Abbo, M.D., Ph.D., University of Chicago
    • Principal Investigator: David Meltzer, M.D., Ph.D., University of Chicago

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of Chicago
    ClinicalTrials.gov Identifier:
    NCT00121004
    Other Study ID Numbers:
    • 13787A
    First Posted:
    Jul 19, 2005
    Last Update Posted:
    Sep 5, 2013
    Last Verified:
    Sep 1, 2013
    Keywords provided by University of Chicago
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 5, 2013