Observational, non-interventional, transversal, multicenter, open label (No treatment is involved). The primary objective is to detect the prevalence of depressive symptoms in bipolar patients admitted to a psychiatric Unit due to an acute mania episode. Secondary objectives include 1) to evaluate, the relationship between depressive symptoms and severity of mania; 2) to evaluate, the relationship between depressive symptoms and anxiety; 3) to evaluate, the relationship between depressive symptoms and psychotic symptoms; 4) to evaluate, the relationship between depressive symptoms and insight; 5) to evaluate, the relationship between depressive symptoms and clinical global impression; 6) to evaluate, the relationship between depressive symptoms and previous treatment with antipsychotics (whatever the antipsychotic was); 7) to evaluate, the relationship between depressive symptoms and length of admission; 8) to evaluate factors (demographic, evolution…) which could be involved in the presence of depressive symptoms within an acute manic episode; 9) to evaluate, the difference on the initial prescription due to the detection of depressive symptoms; 10) to evaluate, if exists, differences on the previous psychiatric diagnosis in patients with and without depressive symptoms. The primary endpoint is score of the MADRS (Montgomery-Asberg Depression Rating Scale) in bipolar patients with acute mania
Study Type
OBSERVATIONAL
Enrollment
250
Research Site
A Coruña, Spain
Research Site
Alcoy, Spain
Research Site
Algeciras, Spain
Research Site
Almería, Spain
Research Site
Barcelona, Spain
Research Site
Burgos, Spain
Research Site
Córdoba, Spain
Research Site
Granada, Spain
Research Site
Las Palmas, Spain
Research Site
Logroño, Spain
...and 24 more locations
Score of the MADRS (Montgomery-Asberg Depression Rating Scale) in bipolar patients with acute mania.
Time frame: once during study
Mania symptoms measured with YMRS (Young Mania Rating Scale).
Time frame: once during study
Anxiety symptoms measures with HARS (Hamilton Anxiety Rating Scale).
Time frame: once during study
Psychotic symptoms measured with BPRS (Brief Psychosis Rating Scale).
Time frame: once during study
Clinical status and improvement measured with CGI-BP (Clinical Global Impression - Bipolar scale).
Time frame: once during study
Days of hospitalization, MADRS (6 items)
Time frame: once during study
Hamilton Depression Rating Scale (5 items)
Time frame: once during study
Scale of Unawareness of Mental Disorders (SUMD)
Time frame: once during study
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