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Psychotic Disorder NOS clinical trials

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NCT ID: NCT02949232 Terminated - Schizophrenia Clinical Trials

Prednisolone Addition for Patients With Recent-onset Psychotic Disorder

Start date: July 2014
Phase: Phase 4
Study type: Interventional

Treatment with prednisolone can be used as a proof of concept to investigate the possibility of immune modulation as a treatment for schizophrenia. It is expected that daily treatment with prednisolone in addition to antipsychotic treatment reduces psychotic symptoms and improves cognition, as compared to placebo. The investigators propose to investigate the effects of administering the corticosteroid prednisolone versus placebo in addition to standard antipsychotic medication in patients with early stage schizophrenia or related disorders, hypothesizing that a decrease in the overall low-grade cerebral inflammation due to prednisolon treatment will be expressed as a decrease in overall symptom severity., Secondly, addition of prednisolone is hypothesised to slow down cognitive deterioration in recent-onset psychosis patients. Finally, the investigators aim to determine whether indirect immunological parameters of the hypothesised low grade inflammation status in schizophrenia are shifted due to the addition of prednisolone.

NCT ID: NCT01888627 Recruiting - Schizophrenia Clinical Trials

Integrated Care in Psychotic Disorders With Severe Mental Illness

ACCESS-II
Start date: May 2007
Phase: N/A
Study type: Interventional

The study examine the effectiveness of an integrated care program including therapeutic assertive community treatment (ACT) for people with psychotic disorders fulfilling severe and persistent mental illness (SPMI, ACCESS-II study).

NCT ID: NCT01339858 Completed - Schizophrenia Clinical Trials

The Effect of N-Acetyl Cysteine on Cortical Erosion in Early Stage Schizophrenia

Breier-Stanley
Start date: May 2011
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to determine if NAC, added to existing antipsychotic treatment, is superior to placebo for cortical erosion in patients with early stage psychosis. The primary hypothesis is that there will be significantly less cortical erosion as measured by cortical thickness, cortical volume and cortical white matter density (assessed by DTI) in patients treated for 12 months with NAC as compared to those treated with placebo. The secondary objectives of this study are to determine if 12 months of NAC add-on treatment is superior to placebo for fMRI determined working memory and semantic memory tasks, cortical MR spectroscopy measures (glutathione, N-acetylaspartate, and glutamine/glutamate levels), electrophysiologically determined attention measures (e.g., mismatch negativity, P300), symptoms, functional measures and cognitive functioning.

NCT ID: NCT01321177 Completed - Schizophrenia Clinical Trials

An Integrated Program for the Treatment of First Episode of Psychosis

RAISE ETP
Start date: July 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how services should be provided to reduce symptoms and improve life functioning for adolescents and adults who have been recently diagnosed with schizophrenia.