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Bipolar Comprehensive Outcomes Study (BCOS)
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Sample details

The Bipolar Comprehensive Outcomes Study (BCOS) is a 2-year observational study designed to explore the clinical and functional outcomes associated with treatment of bipolar I or schizoaffective disorder. The sample comprises adults with a primary diagnosis of bipolar I disorder (manic, mixed or depressed episode) or schizoaffective disorder as defined by the DSM-IV-TR. In addition, all participants have a prescription for at least one of the following mood stabilisers at baseline — olanzapine, lithium carbonate, sodium valproate or carbamazepine.

Study design
Cohort - clinical

Number of participants at first data collection

240 (participants)

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Patients and clinical populations
People with psychiatric conditions
Dataset details

Country

Australia

Year of first data collection

2005

Primary Institutions

Eli Lilly Australia

Mental Health Research Institute

Monash Alfred Psychiatry Research Centre

Orygen Research Centre

University of Melbourne

Links
No website available

Profile paper DOI

doi.org/10.1016/j.jad.2007.08.012

Funders

Eli Lilly Australia

Ongoing?
No

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Interview – face-to-face
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

  • None
  • Keywords

    Clinical cohort
    Mood stabilisers
    Naturalistic design
    Pharmacological treatment
    Quality of life
    Socioeconomics
    Substance use
    Treatment experiences and outcomes
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