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Schizophrenia Treatment Adherence Investigation (STAI)

Not Applicable
Completed
Conditions
Schizophrenia or Schizoaffective disorder
Mental Health - Schizophrenia
Registration Number
ACTRN12607000250437
Lead Sponsor
Janssen-Cilag Pty Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
550
Inclusion Criteria

Clinical diagnosis of Schizophrenia or Schizoaffective Disorder according to DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, 4th Edition). Currently treated in an outpatient clinic. Over 18 years and able to provide informed consent.

Exclusion Criteria

There is no exclusion criteria for this treatment review.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome of this treatment review is to quantify the risk status for medication adherence in a cohort of Australian patients diagnosed with schizophrenia. [ Participant medication adherence will be assessed at baseline, 6 month follow up and 12 month follow up. Follow up will consist of a review of the participants medical records only.]
Secondary Outcome Measures
NameTimeMethod
1. Reporting on the proportion of patients with schizophrenia who may be inappropriately clinically and/or medically treated in the context of their medication adherence risk status. <br>[ Participant medication adherence will be assessed at baseline, 6 month follow up and 12 month follow up. Follow up will consist of a review of the participants medical records only.];2. Quantifying any antipsychotic medication modification and relating this to the treatment review factors captured at baseline. <br>[ Participant medication adherence will be assessed at baseline, 6 month follow up and 12 month follow up. Follow up will consist of a review of the participants medical records only.];3. Relating the adherence risk status to the medications used and the actual acute exacerbation rate.[ Participant medication adherence will be assessed at baseline, 6 month follow up and 12 month follow up. Follow up will consist of a review of the participants medical records only.]
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