Feasibility and Outcomes of Older Patients Hospitalization

The recruitment status of this study is unknown because the information has not been verified recently.
Verified June 2007 by Hillel Yaffe Medical Center.
Recruitment status was  Not yet recruiting
Information provided by:
Hillel Yaffe Medical Center
ClinicalTrials.gov Identifier:
First received: June 20, 2007
Last updated: NA
Last verified: June 2007
History: No changes posted
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.

Condition Intervention
Community-Acquired Pneumonia
Exacerbation of Chronic Heart Failure
Exacerbation of Chronic Obstructive Pulmonary Disease
Procedure: sub-acute hospitalization

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care

Resource links provided by NLM:

Further study details as provided by Hillel Yaffe Medical Center:

Estimated Enrollment: 300
Study Start Date: July 2007
Estimated Study Completion Date: August 2007

Ages Eligible for Study:   65 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00489021

Contact: Doron Nezer, M.D. 972-9-8633272 doronne@clalit.org.il

Sponsors and Collaborators
Hillel Yaffe Medical Center
Principal Investigator: Doron Nezer, M.D. Clalit Health Services, Israel
  More Information

ClinicalTrials.gov Identifier: NCT00489021     History of Changes
Other Study ID Numbers: 20/2007-1-HY-CTIL 
Study First Received: June 20, 2007
Last Updated: June 20, 2007
Health Authority: Israel: Ethics Commission

Keywords provided by Hillel Yaffe Medical Center:
Subacute care
Activities of Daily Living
Cognition assessment
Mood assessment
Incontinence control

Additional relevant MeSH terms:
Lung Diseases, Obstructive
Pulmonary Disease, Chronic Obstructive
Connective Tissue Diseases
Lung Diseases
Pathologic Processes
Respiratory Tract Diseases
Respiratory Tract Infections
Skin Diseases, Infectious

ClinicalTrials.gov processed this record on May 23, 2016