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Family Satisfaction in the Intensive Care Unit - a Multicentre Assessment (Swiss-BEAN)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00890513
First Posted: April 29, 2009
Last Update Posted: November 20, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University Hospital Inselspital, Berne
  Purpose

The primary aim of the present study is to assess satisfaction in a large sample of next of kin in Swiss-German ICUs.

Secondary aims are to test the hypothesis that family satisfaction is related to ICU structure and process and to factors related to patients and next of kin. Further, the hypothesis will be tested that proxy assessment is possible, i.e. next of kin rate satisfaction with care similar to patients.


Condition
Critical Illness

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Family Satisfaction in the Intensive Care Unit - a Multicentre Assessment

Further study details as provided by University Hospital Inselspital, Berne:

Primary Outcome Measures:
  • To assess satisfaction in Swiss-German ICUs

Secondary Outcome Measures:
  • To test the hypothesis that family satisfaction is related to ICU structure and process To test the hypothesis that proxy assessment is possible

Enrollment: 1200
Study Start Date: April 2007
Study Completion Date: December 2007
Primary Completion Date: December 2007 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   16 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Next of kin of patients cared for in one of the 42 ICU's located in german-speaking Switzerland (ICU recognized by Swiss Society of Intensive Care Medicine).
Criteria

Inclusion Criteria:

  • family members of patients staying for > 48 hours in an ICU

Exclusion Criteria:

  • lack of consent,
  • insufficient knowledge of German language
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00890513


Locations
Switzerland
Department of Intenisve Care Medicine, Inselspital
Bern, BE, Switzerland, CH-3010
Sponsors and Collaborators
University Hospital Inselspital, Berne
Investigators
Principal Investigator: Hans U Rothen, MD PhD Bern University Hospital, University of Bern-Switzerland
  More Information

Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Rothen Hans Ulrich, Department of Intensive Care Medicine, University Hospital Bern, Switzerland
ClinicalTrials.gov Identifier: NCT00890513     History of Changes
Other Study ID Numbers: KEK_180/06
First Submitted: April 27, 2009
First Posted: April 29, 2009
Last Update Posted: November 20, 2009
Last Verified: November 2009

Additional relevant MeSH terms:
Critical Illness
Disease Attributes
Pathologic Processes