EULAST-II: European Long-acting Antipsychotics in Schizophrenia Trial-II
Study Details
Study Description
Brief Summary
Schizophrenia is a chronic psychiatric illness with a heterogeneous disease course, varying from periods of symptomatic remission to relapse. Relative to the wealth of scientific data on the course of schizophrenia during the two years following the first psychotic episode, the outcome of schizophrenia patients over the first decade of their illness has been studied to a lesser degree. In this follow-up cohort study we aim to investigate the long-term outcome of schizophrenia patients who participated in the previously conducted EULAST-I clinical trial, in the first decade after being diagnosed.
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Study Design
Outcome Measures
Primary Outcome Measures
- To assess which baseline EULAST-I clinical trial baseline characteristics predict healthcare utilization (defined as number of days hospitalized) over a period of 3 - 10 years (since the EULAST-I clinical trial baseline visit). [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
Secondary Outcome Measures
- To provide insight into long-term social functioning as measured through the Personal and Social Performance (PSP) scale. [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight into long-term sociodemographic outcome (living circumstances, education, marital status). [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight in changes in neuropsychiatric diagnoses as measured through the Mini-International Neuropsychiatric Interview 7.0.2 (M.I.N.I. 7.0.2) since the EULAST-I clinical trial screening visit. [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight in long-term outcome in quality of life as measured through the Euroqol quality of life scale (EQ-5D-5L). [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight in long-term outcome in alcohol and drug use as well as smoking as measured through the Alcohol, Smoking and Substance Involvement Screening Test (ASSIST). [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight in long-term outcome of tardive dyskinesia as measured through the Abnormal and Involuntary Movement Scale (AIMS). [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight in long-term outcome of extrapyramidal symptoms as measured through the St. Hans rating scale. [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight in the use of antipsychotic medication and other medication since the previous EULAST-I clinical trial. [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight into the reasons for hospitalizations since the baseline visit of the previous EULAST-I clinical trial. [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
- To provide insight into the incidence of suicide attempts since the baseline visit of the previous EULAST-I clinical trial [3 - 10 years (since the EULAST-I clinical trial baseline visit).]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Capable of providing written informed consent / have a legal representative to provide written informed consent. *
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Having been randomized to one of the four treatment arms (aripiprazole oral, aripiprazole depot, paliperidone oral, paliperidone depot) in the 2014-002765-30 EULAST-I clinical trial or having participated in the EULAST-I naturalistic cohort study.
- Unless prohibited by local law (e.g. due to incarceration).
Exclusion Criteria: No exclusion criteria are applicable in this study.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Rene Kahn
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 00-000