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Schizophreniform Disorders clinical trials

View clinical trials related to Schizophreniform Disorders.

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NCT ID: NCT03067311 Completed - Clinical trials for Schizophreniform Disorders

Targeting Stress Reactivity in Schizophrenia: Integrated Coping Awareness Therapy

I-CAT
Start date: October 3, 2016
Phase: N/A
Study type: Interventional

To test the feasibility of a clinical trial implementing I-CAT, a novel therapeutic intervention combining strategies to improve stress reactivity and increase meaningful coping, as well as a range of possible proximal (e.g. autonomic, endocrine, immune indices of stress reactivity, symptom severity) and distal measures (function, relapse, quality of life) for 40 people with first episode psychosis in the context of a small randomized controlled trial.

NCT ID: NCT01082588 Completed - Schizophrenia Clinical Trials

Effects of Pravastatin on Cholesterol, Inflammation and Cognition in Schizophrenia

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

This study involves people with schizophrenia or schizoaffective disorder, who are currently taking antipsychotic medications. Some antipsychotic medications may cause an increase in cholesterol levels, which may lead to inflammation in the body. Inflammation poses a risk in developing heart disease, diabetes and problems with brain function. The purpose of this study is to see if pravastatin can: - Lower cholesterol - Decrease inflammation - Improve cognition in patients with schizophrenia

NCT ID: NCT00796081 Completed - Schizophrenia Clinical Trials

A Safety and Pharmacokinetic Study of ER OROS Paliperidone in Pediatric Patients With Schizophrenia, Schizoaffective Disorder, or Schizophreniform Disorder

Start date: January 2006
Phase: Phase 1
Study type: Interventional

The purposes of this study are to characterize the pharmacokinetics of paliperidone after single- and multiple-dose administration of paliperidone ER in children and adolescent patients (>= 10 to <= 17 years of age) with schizophrenia, schizoaffective disorder, or schizophreniform disorder and to evaluate the safety and tolerability of paliperidone ER in this patient population.

NCT ID: NCT00595504 Completed - Schizophrenia Clinical Trials

Ramelteon as an Adjunct Therapy in Non-Diabetic Patients With Schizophrenia

Start date: January 2008
Phase: Phase 4
Study type: Interventional

This study involves people who have schizophrenia or schizoaffective disorder who are currently taking antipsychotic medications. Some antipsychotic medications may cause weight gain and may increase the risk of diabetes mellitus and heart disease.The purpose of this study is to find out what happens if another medication (ramelteon) is used along with your antipsychotic medication. We want to find out whether doing this will: - Change the way your body breaks down fat and sugar. - Affect your waist size, stomach fat and triglycerides (a type of fat in your blood). - Improve how your body responds to insulin. - Affect your quality of sleep. - Reduce movement disturbances Ramelteon is approved by the U.S. Food and Drug Administration (FDA) to treat people that have difficulty falling asleep. It is not approved for such things as affecting waist size or improving how the body breaks down fat and sugar. Its use in this study is investigational.

NCT ID: NCT00515489 Terminated - Schizophrenia Clinical Trials

Study on the Safety and Effectiveness of Risperidone Treatment of Acute Psychotic Patients

Start date: November 2001
Phase: N/A
Study type: Observational

The purpose of this study was to evaluate the safety of risperidone treatment in acute psychotic patients that require an admission into emergency department. The effectiveness of risperidone in controlling acute psychotic symptomatology and incidence, severity and risk of psychomotor agitation in acute psychotic patients was also studied.

NCT ID: NCT00419146 Completed - Schizophrenia Clinical Trials

Treatment of Schizophrenia With an Omega-3 Fatty Acid (EPA) and Antioxidants

Start date: September 2001
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this trial is to study the effect of adding the omega-3 fatty acid EPA and/or Vitamins E + C to antipsychotic drugs in younger patients with schizophrenia and related psychoses.

NCT ID: NCT00407277 Completed - Schizophrenia Clinical Trials

Neural Inhibition as a Mechanism of Nicotine Dependence Among Persons With Schizophrenia

Start date: February 2007
Phase: N/A
Study type: Interventional

Cigarette smoking decreases life expectancy, causes devastating health complications, and costs society billions of dollars each year. These untoward consequences are especially pronounced among persons with schizophrenia (SCZ) because approximately 80% to 95% of this group smokes cigarettes. These high prevalence rates underscore the need for research investigating the determinants of smoking in patients with SCZ. Several researchers have observed that nicotine improves specific symptoms of SCZ including negative symptoms, negative affect, and cognitive deficits. This has led to the hypothesis that patients with SCZ smoke in an attempt to self-medicate. However, the mechanism(s) by which nicotine has its positive effect on symptoms remains unclear. The current proposal posits that neural inhibition (NI) is a physiological mechanism of this effect, while variation in the alpha-7-nicotinic receptor subunit gene (CHRNA7) represents the genetic underpinnings of these processes. The proposed study will assess NI and symptom improvement after acute administration of nicotine to both smokers and nonsmokers with SCZ. In addition, NI and CHRNA7 variation will be tested as predictors of patients' ability to reduce/quit smoking following smoking treatment. These data may lead to the development of new pharmacological strategies for treating the symptoms of SCZ and new methods for assisting these patients to quit smoking.

NCT ID: NCT00222495 Completed - Schizophrenia Clinical Trials

A Comparative Study of New Medications for Psychosis in Adolescents

Start date: August 2002
Phase: N/A
Study type: Interventional

The overall goal of this study is to determine the efficacy and tolerability of three atypical antipsychotic medications (risperidone, olanzapine, and quetiapine) in the treatment of adolescents with psychosis. It is hypothesized that the three medications will be equally effective in reducing the symptoms of psychosis.

NCT ID: NCT00161057 Completed - Schizophrenia Clinical Trials

Functional Brain Activation Patterns in Schizophrenia, Measured Before and After Treatment

Start date: December 2001
Phase: N/A
Study type: Observational

In this study we, the investigators at UMC Utrecht, intend to investigate changes in brain activation patterns using functional magnetic resonance imaging (MRI), in patients suffering from schizophrenia who are medication naive or off medication, before using medication and after 8 weeks of medication. Patients will perform a working memory task, a language task and a motor task while lying in the scanner. We hypothesize that the efficiency of the working memory system is reduced and that the lateralization of language is diminished in these patients, and that these functions will normalize after treatment.

NCT ID: NCT00157313 Active, not recruiting - Clinical trials for Schizoaffective Disorder

Clinical Trial of Integrated Treatment Versus Standard Treatment in First Episode Psychosis

Start date: January 1998
Phase: N/A
Study type: Interventional

The purpose of the study was to evaluate the effects of integrated treatment for patients with a first episode of psychotic illness. We conducted a randomised clinical trial in Copenhagen Hospital Corporation and Psychiatric Hospital Aarhus, Denmark. We included 547 patients with first episode of schizophrenia spectrum disorder, who has not received antipsychotic medication for more than 12 weeks. Patients were randomised to integrated treatment or standard treatment. The integrated treatment lasted for two years and consisted of assertive community treatment with programmes for family involvement and social skills training. Standard treatment offered contact with a community mental health centre. We wanted to study the effect on psychotic (hallucinations and delusions)and negative (lack of initiative, apati, blunted affect) symptoms (each scored from 0 to a maximum of 5) at one and two years' follow-up. We found that integrated treatment improved clinical outcome and adherence to treatment. The improvement in clinical outcome was consistent at one year and two year follow-ups. We will study further outcome measures such as social network, quality of life, depression and suicidal behaviour.