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Quality Project to Evaluate and Validate the FAST-O Rating Scale (FAST-O)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00913731
First Posted: June 4, 2009
Last Update Posted: October 29, 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:
AstraZeneca
June 2, 2009
June 4, 2009
October 29, 2009
May 2009
Not Provided
Reliability test of the FAST-O rating scale based on observational symptom ratings of patients with acute psychotic diseases [ Time Frame: Each patients symtoms will be rated on 2 occasions, by 2-3 raters, each. First is made within 24 hrs of admission to acute psychiatric care, secondis made 14 +/- 2 days after admittance, or earlier if the patient is discharged. ]
Reliability test of the FAST-O rating scale based on observational symptom ratings of patients with acute psychotic diseases [ Time Frame: Each patient will be assessed on 2-3 occasions ]
Complete list of historical versions of study NCT00913731 on ClinicalTrials.gov Archive Site
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Quality Project to Evaluate and Validate the FAST-O Rating Scale
Quality Project to Evaluate and Validate the FAST-O Rating Scale (Fast ASessment in Acute Treatment of Psychosis-Observation)
The purpose of this project is to test the reliability of the FAST-O Rating Scale in patients at acute wards or psychiatric intensive care units.
Not Provided
Observational
Time Perspective: Prospective
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Non-Probability Sample
Patients with acute psychotic symptoms attending the acute ward or psychiatric intensive care unit
Acute Psychotic Symptoms
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psychotic patients
psychotic patients, acute ward, symptom rating scale.
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
111
October 2009
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Inclusion Criteria:

  • Patients with acute psychotic symptoms attending the acute ward or psychiatric intensive care unit

Exclusion Criteria:

Sexes Eligible for Study: All
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
Sweden
 
 
NCT00913731
NIS-NSE-DUM-2008/1
No
Not Provided
Not Provided
AstraZeneca
AstraZeneca
Not Provided
Study Director: Eva Dencker Vansvik Medical Department
Principal Investigator: Eva Lindström Rättspsyk, UMAS, Malmö
AstraZeneca
October 2009