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A Study to Tailor Advance Directives

NCT00121004 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2013-09-05

No results posted yet for this study

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.

Conditions

  • Dementia
  • Persistent Vegetative State
  • Terminally Ill

Interventions

BEHAVIORAL

Advance Directive Selection

Sponsors & Collaborators

  • University of Chicago

    lead OTHER

Principal Investigators

  • Elmer Abbo, M.D., Ph.D. · University of Chicago

  • David Meltzer, M.D., Ph.D. · University of Chicago

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2005-09-30
Completion
2005-09-30

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00121004 on ClinicalTrials.gov