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Feasibility and Outcomes of Older Patients Hospitalization

Primary Purpose

Community-Acquired Pneumonia, Exacerbation of Chronic Heart Failure, Exacerbation of Chronic Obstructive Pulmonary Disease

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
sub-acute hospitalization
Sponsored by
Hillel Yaffe Medical Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Community-Acquired Pneumonia focused on measuring Subacute care, Activities of Daily Living, Cognition assessment, Mood assessment, Incontinence control

Eligibility Criteria

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

Inclusion Criteria:

  • Age over 65
  • Hemodynamic, nutritional and respiratory stability
  • eligibility for sub- acute hospitalization

Exclusion Criteria:

  • Oncological active disease
  • uncorrectable hypoxemia (oxygen saturation 90%),
  • suspected myocardial ischemia
  • presence of an acute illness, other than the target illness

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    June 20, 2007
    Last Updated
    June 20, 2007
    Sponsor
    Hillel Yaffe Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00489021
    Brief Title
    Feasibility and Outcomes of Older Patients Hospitalization
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2007
    Overall Recruitment Status
    Unknown status
    Study Start Date
    July 2007 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    August 2007 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Hillel Yaffe Medical Center

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Hospitalization is a traumatic event for the patient and his family at any age nevertheless in the older age. One of its consequences is the difficulty to resume previous activity of daily living especially in older (over 75 years) patients. Sub acute completes the acute phase of the hospitalization and its main purpose is to improve the patient's functional status and quality of life. There are not enough clinical trails to proof this assumption. The purpose of our study is to compare the outcome of acute and sub-acute hospitalization programs by a randomized controlled prospective intervention study. Outcome measures will comprise activity of daily living, functional status, re-hospitalization and utilization of medical services following the hospitalization.Study hypothesis is that sub-acute hospitalization will improve outcomes and will cost less.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Community-Acquired Pneumonia, Exacerbation of Chronic Heart Failure, Exacerbation of Chronic Obstructive Pulmonary Disease, Cellulitis
    Keywords
    Subacute care, Activities of Daily Living, Cognition assessment, Mood assessment, Incontinence control

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    300 (Anticipated)

    8. Arms, Groups, and Interventions

    Intervention Type
    Procedure
    Intervention Name(s)
    sub-acute hospitalization

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age over 65 Hemodynamic, nutritional and respiratory stability eligibility for sub- acute hospitalization Exclusion Criteria: Oncological active disease uncorrectable hypoxemia (oxygen saturation 90%), suspected myocardial ischemia presence of an acute illness, other than the target illness
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Doron Nezer, M.D.
    Phone
    972-9-8633272
    Email
    doronne@clalit.org.il
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Doron Nezer, M.D.
    Organizational Affiliation
    Clalit Health Services, Israel
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Feasibility and Outcomes of Older Patients Hospitalization

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