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Psychotic Disorders clinical trials

View clinical trials related to Psychotic Disorders.

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NCT ID: NCT01196286 Completed - Schizophrenia Clinical Trials

Multifamily Psychoeducation and Cognitive Remediation for Recent-Onset Psychosis

Start date: June 2010
Phase: N/A
Study type: Interventional

The goal of this study is to determine whether pairing multifamily group psychoeducation with cognitive remediation may facilitate improved outcomes among individuals with recent-onset psychosis.

NCT ID: NCT01193153 Completed - Clinical trials for Schizoaffective Disorder

A Study to Evaluate the Efficacy of Paliperidone Palmitate in the Prevention of Relapse of the Symptoms of Schizoaffective Disorder

Start date: September 2010
Phase: Phase 3
Study type: Interventional

This study will evaluate the efficacy of paliperidone palmitate compared with placebo in the delay of relapse of the symptoms of schizoaffective disorder. This study will also assess the safety and tolerability of paliperidone palmitate in patients with schizoaffective disorder.

NCT ID: NCT01182012 Recruiting - Schizophrenia Clinical Trials

Reduction of Cardiovascular Risk in Severe Mental Illness

RISCA-TMS
Start date: August 2010
Phase: Phase 4
Study type: Interventional

Background: Patients with severe mental illness (SMI) have a higher prevalence of cardiovascular risk factors (CVRF) than the general population and a control of these risk factors poorer. Serious mental illness often causes health teams to focus interventions in mental illness and put aside the CVRF. Objectives: This project aims to assess the CVRF, stratify the cardiovascular risk, adequate drug treatment to reduce this risk and evaluate the effectiveness of an intervention by professional community nurses in patients with SMI. Materials and Methods: Prospective study of a cohort of patients over 18 years with a diagnosis of SMI with two cross sections to evaluate the cardiovascular risk and adequacy of drug treatment. The investigators calculate the risk to the cardiovascular risk tables with the SCORE (Systematic Coronary Risk Evaluation) for countries of low cardiovascular risk and the of Framingham REGICOR (Heart registry of Girona, Spain). The adequacy of pharmacotherapy will be assessed contrasting it with the recommendations of the Program of Preventive Activities and Health Promotion of Family medical association. The intervention will be conducted by professional nurses and consist of an initial psycho-educational intervention, and two more reinforcement throughout twelve months, of duration less than 30 minutes that will be addressed in an integrated manner the clinical situation with regard to cardiovascular risk. If necessary, pharmacological treatment will be prescribed. Twelve months after the first intervention, a second evaluation on cardiovascular risk and the effectiveness of the intervention will be performed.

NCT ID: NCT01181635 Active, not recruiting - Mental Disorders Clinical Trials

Can Psychotherapy Reduce Sickness Absence?

Start date: August 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to examine if psychotherapy can reduce sickness absence.

NCT ID: NCT01175642 Completed - Schizophrenia Clinical Trials

Cognitive Remediation and Functional Skills Training in Schizophrenia

Start date: July 2007
Phase: Phase 0
Study type: Interventional

This randomized trial is examining whether a treatment called cognitive remediation is more effective when it is paired with a social and functional skills training component.

NCT ID: NCT01174004 Completed - Clinical trials for Parkinson's Disease Psychosis

A Study of the Safety and Efficacy of Pimavanserin in Patients With Parkinson's Disease Psychosis

Start date: July 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of 40 mg pimavanserin compared to placebo in patients with Parkinson's disease psychosis (PDP).

NCT ID: NCT01173874 Recruiting - Schizophrenia Clinical Trials

Efficacy of Cognitive Remediation in Patients With Schizophrenia or Schizoaffective Disorder Stabilized on Lurasidone

Start date: July 2010
Phase: Phase 3
Study type: Interventional

The investigators hypothesize that cognitive remediation will be superior to the active control group on the change from baseline to study end point of cognitive remediation phase on both co-primary outcome measures (standardized composite MATRICS score and Cognitive Assessment Interview).

NCT ID: NCT01172106 Recruiting - Clinical trials for Postpartum Psychosis

Impact of Family Psychoeducation on Psychosis

Start date: August 2008
Phase: N/A
Study type: Interventional

There is currently no clear involvement of families/caregivers in the care for postpartum mothers that develop postpartum psychosis. The lack of knowledge on causes of postpartum psychosis may influence the nature of perceived social support that mothers receive from caregivers. It is hoped that the provision of a culturally adapted version of family psychoeducation will bridge the knowledge gap and provide the much needed information. We therefore hypothesized that the involvement of a family member of a postpartum mother with a psychotic illness in a weekly session of family psychoeducation.

NCT ID: NCT01169142 Completed - Schizophrenia Clinical Trials

Study of Vitamin D in the Severely Mentally Ill

Start date: January 2010
Phase: Phase 4
Study type: Interventional

Supplementation of Vitamin D in those with low levels will increase the level and result in some improvement in health and psychopathology measures.

NCT ID: NCT01162434 Completed - Mental Disorders Clinical Trials

Brain MRI (Magnetic Resonance Imaging) Scans of Patients With Treatment Resistant Depression (TRD) and Healthy Controls

Start date: February 2010
Phase: N/A
Study type: Observational

Treatment resistant depression (TRD) is a major health concern, with 10% of patients with major depressive disorder not responding to conventional treatments. The investigators propose to compare the MRI (magnetic resonance imaging) brain scans of patients with TRD, which were collected during surgical planning for deep brain stimulation, with age, sex, handedness and education-matched healthy volunteer controls, to investigate anatomical differences, specifically the volume of certain brain structures.