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Schizoaffective Disorder clinical trials

View clinical trials related to Schizoaffective Disorder.

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NCT ID: NCT00337662 Completed - Schizophrenia Clinical Trials

Efficacy Study of Early Onset of Antipsychotic Drug Action in Schizophrenia

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

The current study has been designed to address the significance of early onset of response prospectively in patients treated with an atypical antipsychotic.

NCT ID: NCT00330863 Completed - Schizophrenia Clinical Trials

Preventing Relapse in Schizophrenia: Oral Antipsychotics Compared To Injectables: Evaluating Efficacy

PROACTIVE
Start date: May 2006
Phase: Phase 4
Study type: Interventional

This study is designed to find out whether taking antipsychotic medication once every two weeks by injection compared to taking daily oral medication will help people with schizophrenia maintain better control of their symptoms.

NCT ID: NCT00325689 Completed - Schizophrenia Clinical Trials

Aripiprazole Used as Dual Therapy in the Treatement of Patients With Chronic Stable Schizophrenia or Schizoaffective Disorder.

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

A Multicenter, Double-blind 16 Week Study on the augmentation of atypical antipsychotic with Aripiprazole in patients with Schizophrenia with inadequate response to antipsychotic treatment.

NCT ID: NCT00320736 Completed - Schizophrenia Clinical Trials

Galantamine for Cognition in People With Schizophrenia

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

This study is a double-blind, placebo-controlled trial of the nicotinic receptor agonist, galantamine, for the improvement of memory and attention in people with schizophrenia and schizoaffective disorder. Twenty subjects on a stable dose of antipsychotic medications receive galantamine or identical placebo tablets for 8 weeks. Adverse events are screened for every week. Tests of memory, attention, and reward responsivity are performed at baseline and afer 8 weeks on medication. Clinical scales rating psychiatric symptoms are performed at the beginning, middle, and end of the trial.

NCT ID: NCT00320723 Completed - Schizophrenia Clinical Trials

Nicotine Replacement Therapy for Smoking Cessation in Schizophrenia

Start date: July 2001
Phase: Phase 4
Study type: Interventional

This proposal seeks to evaluate a pilot smoking cessation treatment program that will combine nicotine replacement therapy with or without bupropion sustained-release (SR) with cognitive behavioral therapy for smoking cessation in patients with major mental illness.

NCT ID: NCT00320697 Completed - Schizophrenia Clinical Trials

Smoking Relapse Prevention in Schizophrenia

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

This study seeks to determine if continued treatment with bupropion and nicotine replacement therapy (NRT) can reduce the smoking relapse rate in patients with schizophrenia.

NCT ID: NCT00316303 Completed - Depression Clinical Trials

Effectiveness of the Screen, Test, Immunize, Reduce Risk, and Refer (STIRR) Intervention for People With Both a Mental and Substance Abuse Disorder

Start date: February 2006
Phase: Phase 2
Study type: Interventional

This study will determine the effectiveness of the STIRR (Screen, Test, Immunize, Reduce risk, and Refer) intervention in increasing rates of testing, immunization, referral, and treatment for blood-borne diseases, such as hepatitis and HIV, in people with both a mental disorder and a substance abuse disorder.

NCT ID: NCT00313391 Completed - Schizophrenia Clinical Trials

Risperdal Consta and Health Care Utilization in Patients With Schizophrenia

Start date: December 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if Risperdal Consta will affect the healthcare utilization costs in chronically ill schizophrenic patients with multiple admissions to the psychiatric hospital compared to the previous utilization costs under standard oral treatment of any atypical antipsychotic. We hypothesize that higher Risperdal Consta acquisition costs can be offset by reduction in total medical utilization costs, such as hospitalizations, ER visits, unscheduled outpatient visits or incarcerations due to worsening of psychotic symptoms.

NCT ID: NCT00312598 Completed - Schizophrenia Clinical Trials

Body Mass Index (BMI) and Metabolic Changes Following Switch to Aripiprazole From Olanzapine, Risperidone and Quetiapine

Start date: August 2005
Phase: Phase 4
Study type: Observational

Weight gain is a serious, common side effect of many antipsychotic medications. On average, the highest amounts of weight gain are found to occur in people taking clozaril and olanzapine, but with significant weight gain occuring in those on the other atypical antipsychotics as well. We, the researchers at the University of North Carolina, propose an open-label observational, pilot study of the changes in weight, BMI, body composition, and lipids, glucose, insulin and other metabolic parameters occurring in subjects as they switch from treatment with olanzapine, risperidone or quetiapine to aripiprazole. This medication switch will be determined prior to their entering this study by their treating psychiatrist. We also will determine resting energy expenditure (REE) and respiratory quotient (RQ) as measured by metabolic cart to determine if either energy expenditure or the propensity to store energy as fat may be involved in any changes to weight that are detected. Food intake, hunger, and physical activity will also be assessed.

NCT ID: NCT00306475 Completed - Schizophrenia Clinical Trials

Does The Addition Of Divalproex Sodium ER To An Atypical Antipsychotic Drug (APD) Improve Cognition And Psychopathology In Outpatients With Schizophrenia (SCH) Or Schizoaffective Disorder (SAD)?

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

The major objective of this proposal is to test the hypothesis that the addition of divalproex sodium to an atypical antipsychotic drug other than clozapine will significantly improve: a) cognition; and b) psychopathology (positive, negative, and mood symptoms) in a double-blind, randomized trial of 6 weeks duration in patients with schizophrenia or schizoaffective disorder.