Group Cognitive-behavioral Intervention for Social Anxiety in Schizophrenia
Social AnxietySchizophreniaThis study will explore the helpfulness of a short psychological group treatment called cognitive-behavioral therapy, or CBT. CBT is a form of therapy that is very structured and it aims to improve difficulties that are related to behaviors and emotions by first working on identifying and changing negative inaccurate thoughts. The main goal of this intervention is to see if group CBT reduces the symptoms of social anxiety in people with schizophrenia so that they can improve their social functioning and help their psychotic symptoms. The study compares the usefulness of adding CBT to standard services.
Clinical Risk State for Bipolar Disorder in Adolescents
Bipolar DisorderSchizophreniaAim: The purpose of the study is to characterize the at-risk phases preceding a first episode of bipolar disorder and of schizophrenia, and to identify clinical and biological predictors of the disease development. Hypothesis a: Over 6-24 months, 25% of at-risk youth will develop the full manifestations of Bipolar Disorder (BPD) or schizophrenia. Hypothesis b: The symptoms utilized for characterizing the at-risk phase of BPD will differentiate between individuals developing BPD and schizophrenia.
Work Activity Augmented by Cognitive Rehabilitation for Schizophrenia
SchizophreniaSchizoaffective DisorderThis research investigates the benefits of productive activity and cognitive rehabilitation for patients with schizophrenia. Key questions are: does cognitive rehabilitation plus work activity produce better outcomes than work activity alone? Is cognitive rehabilitation more helpful for individuals with moderate or greater cognitive impairment than for individuals without such impairment? Does cognitive rehabilitation reduce the dropout rate and increase participation in work activity for cognitively impaired subjects? What features of cognitive rehabilitation are most important for clinical and rehabilitation outcomes?
Comparing the Effect of Under the Tongue Olanzapine Versus Swallowed Olanzapine on Body Mass Index...
SchizophreniaSchizoaffective Disorder1 moreThis study is testing if under the tongue olanzapine for schizophrenia, related psychosis, schizoaffective disorder or bipolar disorder will have less weight gain than olanzapine that is swallowed, in patients who are already gaining weight on olanzapine.
Olanzapine Pamoate Depot Versus Oral Olanzapine on Treatment Outcomes in Outpatients With Schizophrenia...
SchizophreniaTo compare the health outcome of patients with schizophrenia, who are at risk for relapse, when treated with a long acting injection form of olanzapine versus treatment with oral olanzapine.
Efficacy Study of Early Onset of Antipsychotic Drug Action in Schizophrenia
SchizophreniaSchizoaffective Disorder1 moreThe current study has been designed to address the significance of early onset of response prospectively in patients treated with an atypical antipsychotic.
5HT3 Antagonism and Auditory Gating in Schizophrenia
SchizophreniaThe target groups in this study are brain waves and neurotransmitters (chemical messengers) in the brain. Subjects with diagnosed with schizophrenia will be studied. The study will help understand more about normal brain functioning and how that functioning differs in people with schizophrenia. Another purpose of this study is to determine how the altered brain functioning in schizophrenia contributes the symptoms found in the illness.
Olanzapine Versus An Active Comparator in the Treatment of Schizophrenia
SchizophreniaThe purpose of this study is to determine how Olanzapine compares to an active comparator in the treatment of schizophrenia
A Study of the Cataractogenic Potential of Seroquel and Risperdal in the Treatment of Participants...
SchizophreniaSchizoaffective DisorderThis Phase IV, randomized, parallel-group study is designed to evaluate the cataractogenic potential of quetiapine fumarate (SEROQUEL) compared with that of a putative non-cataractogenic antipsychotic medication risperidone (RISPERDAL). This study is being conducted to fulfill the SEROQUEL Phase IV commitment regarding evaluation of cataractogenic potential.
To Evaluate the Impact of Treatment Interruption on Re-initiation of Bifeprunox
SchizophreniaSchizoaffective DisorderThe purpose of this study is to investigate a safe treatment interruption interval(s) for re-initiation of bifeprunox at a therapeutic dose. The study duration is approximately 7 to 10 weeks.