Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
300 participants
INTERVENTIONAL
2009-03-31
2010-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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Control
Questionnaire
No interventions assigned to this group
Intervention
Standardized explanation followed by questionnaire
Standardized explanation
Standardized explanation provided on code status, advance directives and end of life care
Interventions
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Standardized explanation
Standardized explanation provided on code status, advance directives and end of life care
Eligibility Criteria
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Inclusion Criteria
* Admitted to regular nursing floor
Exclusion Criteria
* admitted in ICU
* positive screening for depression
* terminal illness defined as life expectancy\< 100 days
* inability to consent
18 Years
ALL
No
Sponsors
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Partners in Internal Medicine
OTHER
Responsible Party
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Principal Investigators
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George Abraham, MD
Role: PRINCIPAL_INVESTIGATOR
Saint Vincent Hospital
Kriti Mittal, MD
Role: PRINCIPAL_INVESTIGATOR
Saint Vincent Hospital
Locations
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Saint Vincent Hospital
Worcester, Massachusetts, United States
Countries
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Other Identifiers
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SVH 1195
Identifier Type: -
Identifier Source: org_study_id
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