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Schizoaffective Disorder clinical trials

View clinical trials related to Schizoaffective Disorder.

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NCT ID: NCT00246259 Completed - Schizophrenia Clinical Trials

A Trial Comparing Risperidone Long-Acting Injection With Oral Antipsychotic in the Treatment of Early Psychosis

Start date: October 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effectiveness, safety and tolerability of risperidone long-acting injection (LAI) versus oral antipsychotics in participants with recent onset psychosis (abnormal thinking and/or hallucinations).

NCT ID: NCT00237848 Completed - Schizophrenia Clinical Trials

D-Serine for Enhancing Cognitive Retraining for the Treatment of Schizophrenia

Start date: February 2005
Phase: Phase 3
Study type: Interventional

This study will examine the effectiveness of D-serine in increasing and sustaining the benefits of cognitive retraining in people with schizophrenia.

NCT ID: NCT00237796 Completed - Schizophrenia Clinical Trials

Functional Rehabilitation of Older Patients With Schizophrenia

Start date: February 2005
Phase: N/A
Study type: Interventional

The primary purpose of this project is to evaluate the efficacy of a group therapy intervention, cognitive behavioral social skills training (CBSST), that teaches social functioning skills and cognitive-behavioral compensatory aids to older patients with schizophrenia. CBSST, therefore, targets the multidimensional deficits that lead to disability in aging veterans with severe mental illness.

NCT ID: NCT00231335 Completed - Schizophrenia Clinical Trials

Efficacy and Safety Study of Escitalopram Augmentation in Treatment Resistant Schizophrenia

Start date: March 2006
Phase: Phase 4
Study type: Interventional

A primary hypothesis to be explored here is that, given its pharmacodynamic profile and hypothesized mechanisms associated with schizophrenia, escitalopram will, in comparison to placebo, be effective when added to risperidone or olanzapine treated group in reducing the severity of resistant symptoms, particularly existing subsyndromal anxiety and depression.

NCT ID: NCT00224822 Completed - Schizophrenia Clinical Trials

The Effects of Aripiprazole on Patients With Metabolic Syndrome

Start date: March 2004
Phase: Phase 4
Study type: Interventional

The primary goal of this study is to assess the effect of aripiprazole on patients who developed metabolic syndrome while taking other second generation antipsychotic medications.

NCT ID: NCT00223418 Completed - Clinical trials for Schizoaffective Disorder

Study Comparing Patients Taking Olanzapine and Patients Taking Aripiprazole on Learning of Vocational Skills

Start date: January 2004
Phase: N/A
Study type: Interventional

STUDY PURPOSE: To study whether patients who have schizophrenia or schizoaffective disorder and are randomly assigned to switch to aripiprazole prior to participation in a brief vocational skills training (VST) will have improved cognitive functioning and learn more in VST than those randomly assigned to stay on olanzapine. There is evidence that VST is important in improving role functioning for schizophrenia patients, however, cognitive impairments limit the ability of some patients to benefit from skills training approaches. Patients switched from olanzapine to aripiprazole improve in terms of verbal learning and verbal learning has been shown to be a strong predictor of community outcome. It is unclear whether the cognitive benefits of switching to aripiprazole extend to improve learning of vocational skills.

NCT ID: NCT00222807 Completed - Schizophrenia Clinical Trials

Schizophrenia, Antipsychotic Treatment and the Risk for Diabetes Mellitus

Start date: August 2003
Phase: N/A
Study type: Observational

This preliminary study aims to investigate the mechanism of higher rates of type 2 diabetes mellitus in patients with schizophrenia. As part of the study, we collect neuroendocrine-immune data on patients with first episode, treatment naive psychosis, patients with newly diagnosed schizophrenia and normal healthy controls. Regardless the treatment status, we collect the same neuroendocrine-immune data on the participants after 2 months.

NCT ID: NCT00222794 Completed - Schizophrenia Clinical Trials

A Clinical Trial to Examine Effects of Atomoxetine in the Treatment of Negative Symptoms in Patients With Schizophrenia

Start date: November 2003
Phase: Phase 4
Study type: Interventional

This study proposes to examine the effect of atomoxetine on quality of life and negative symptoms such as social withdrawal, lack of interest in things, lack of thought content, flat emotions, slowed body movements and lack of drive and motivation in patients with schizophrenia or schizoaffective disorder. This study also examines the safety of using atomoxetine along with the conventional antipsychotic in these patients.

NCT ID: NCT00222235 Completed - Schizophrenia Clinical Trials

Adjunctive Treatment for Decreasing Symptoms of Schizophrenia

Start date: January 2000
Phase: Phase 2/Phase 3
Study type: Interventional

This study will determine the effectiveness of treatment with glycine or d-cycloserine in addition to a normal antipsychotic regimen in improving negative symptoms and cognitive impairments in patients with schizophrenia.

NCT ID: NCT00215579 Completed - Schizophrenia Clinical Trials

Determining the Effects of Risperdal Consta in Patients With Psychotic Disorders and Incomplete Adherence

Start date: April 2004
Phase: Phase 4
Study type: Interventional

As many as 75 percent of patients with schizophrenia have difficulty taking their oral medication on a regular basis. This may lead to worsening of symptoms. Clinicians commonly respond to these problems by adding adjunctive medications, despite the absence of systematic studies that support such practices. It is possible, however, that in many of these cases, the unstable course and/or unsatisfactory treatment response reflects incomplete adherence with the originally prescribed oral antipsychotic, rather than a need for adjunctive medications. This study will examine whether switching patients who demonstrate an unstable course and/or an unsatisfactory clinical response to a long-acting injectable preparation as the primary antipsychotic may enhance medication adherence and improve outcomes.