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Validation of the Korean Confusion Assessment Method for the Intensive Care Unit (CAM-ICU)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00998387
First Posted: October 20, 2009
Last Update Posted: October 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:
Seoul National University Hospital
  Purpose
The purpose of this study is to translate and validate the CAM-ICU for use in the Korean ICU setting.

Condition
Critical Care

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Translation and Validation of the Korean Version of Confusion Assessment Method for the Intensive Care Unit

Further study details as provided by Seoul National University Hospital:

Primary Outcome Measures:
  • Interrater reliability of Korean CAM-ICU [ Time Frame: after completion of study ]
  • Sensitivity of Korean CAM-ICU for diagnosing ICU delirium [ Time Frame: after completion of study ]
  • Specificity of Korean CAM-ICU for diagnosing ICU delirium [ Time Frame: after completion of study ]

Enrollment: 63
Study Start Date: July 2008
Study Completion Date: March 2009
Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
medical ICU
admitted to medical ICU at Seoul National University Hospital longer than 24 hours

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients admitted to medical ICU at Seoul National University Hospital longer than 24 hours
Criteria

Inclusion Criteria:

  • older than 18 years
  • admitted to medical ICU at Seoul National University Hospital longer than 24 hours

Exclusion Criteria:

  • comatose or moribund state throughout the study period
  • preexisting neurologic problem
  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): NCT00998387


Locations
Korea, Republic of
Seoul National University Hospital
Seoul, Korea, Republic of, 110-744
Sponsors and Collaborators
Seoul National University Hospital
Investigators
Principal Investigator: Sang Min Lee, MD Seoul National University Hospital
  More Information

Responsible Party: Sang Min Lee M.D, Seoul National University Hospital
ClinicalTrials.gov Identifier: NCT00998387     History of Changes
Other Study ID Numbers: 0803-058-239
First Submitted: October 16, 2009
First Posted: October 20, 2009
Last Update Posted: October 20, 2009
Last Verified: October 2009

Additional relevant MeSH terms:
Confusion
Neurobehavioral Manifestations
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms


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