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Schizoaffective Disorder clinical trials

View clinical trials related to Schizoaffective Disorder.

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NCT ID: NCT03037983 Completed - Schizophrenia Clinical Trials

Improving Neurocognitive Deficits and Function in Schizophrenia With Transcranial Magnetic Stimulation

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether repetitive transcranial magnetic stimulation (rTMS) is effective in remediating cognitive deficits while also improving functionality in Veterans with schizophrenia.

NCT ID: NCT02978599 Completed - Schizophrenia Clinical Trials

Clinical Trial of AVL-3288 in Schizophrenia Patients

Start date: November 2016
Phase: Phase 1
Study type: Interventional

Single-center, outpatient, randomized, double-blind, placebo-controlled, 3-treatment-phase, cross-over study to evaluate the safety, tolerability and efficacy of two oral doses of AVL-3288 each compared to placebo, in patients with schizophrenia.

NCT ID: NCT02930005 Completed - Schizophrenia Clinical Trials

Pentosan Polysulfate Sodium and Meclofenamic Acid as Treatments in Patients With Psychotic Disorders

Start date: August 7, 2015
Phase: Phase 2
Study type: Interventional

This study evaluates the feasibility of administering meclofenamic acid or pentosan polysulfate sodium as an adjunctive treatment to patients diagnosed with a psychotic disorder. Half of participants will receive meclofenamic acid, while the other half will receive polysulfate sodium.

NCT ID: NCT02921243 Completed - Schizophrenia Clinical Trials

Schizophrenia and the Gut Microbiome

Start date: October 1, 2016
Phase:
Study type: Observational

In a sample of 20 inpatients with a DSM-IV-TR/DSM 5 diagnosis of schizophrenia or schizoaffective disorder, investigators propose to conduct a prospective, 2 week observational trial to collect gastrointestinal stool samples in order to characterize the microbiota in people with schizophrenia and examine its variability over time. Participants may elect to participate for an additional two weeks, during which they will receive the prebiotic, oligofructose-enriched inulin (FOS), in order to examine its effects on the relative preponderance of butyrate-producing bacteria in the gut microbiome. Investigators will use an inpatient sample in order to standardize meals, exercise and environmental mediators. This is considered a feasibility, pilot study in order to apply for future grant funding. Investigators will recruit patients from the Treatment Research Program inpatient unit, Maryland Psychiatric Research Center, University of Maryland School of Medicine.

NCT ID: NCT02901587 Completed - Schizophrenia Clinical Trials

Study Investigating the Effect of Lu AF35700 on Cardiac Repolarization in Men and Women With Schizophrenia and Schizoaffective Disorder

Start date: September 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the effect of Lu AF35700 on electrical activity in the heart as measured on an electrocardiogram (ECG) in patients with schizophrenia or schizoaffective disorder after 6 weeks of treatment

NCT ID: NCT02869334 Completed - Schizophrenia Clinical Trials

Remediation of Auditory Recognition in Schizophrenia With tDCS

Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether transcranial direct current stimulation (tDCS), when combined with different forms of computer based training, improves the ability to discriminate small differences between sounds in people diagnosed with schizophrenia or schizoaffective disorder.

NCT ID: NCT02823041 Completed - Schizophrenia Clinical Trials

Enhancing Cognitive Training Through Exercise Following a First Schizophrenia Episode

CT&E-RCT
Start date: October 13, 2016
Phase: N/A
Study type: Interventional

This is a confirmatory randomized controlled trial of the efficacy of a novel intervention combining neuroplasticity-based cognitive training with aerobic exercise, compared to the same systematic cognitive training alone. Treatment occurs for 6 months after randomization, with a followup assessment at 12 months. The investigators hypothesize that combining neuroplasticity-based computerized cognitive training and neurotrophin-enhancing physical exercise will produce neurotrophin increases and cognitive and functional improvements, even relative to cognitive training alone. The investigators target the period shortly after a first episode of schizophrenia to maximize the generalization of cognitive improvement to functional outcome, before chronic disability is established.

NCT ID: NCT02819349 Completed - Schizophrenia Clinical Trials

Texting for Relapse Prevention

T4RP
Start date: March 12, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether Texting for Relapse Prevention (T4RP), a text messaging-based early warming for relapse prevention in people who have schizophrenia/SAD, is associated with fewer relapse symptoms compared to a treatment-as-usual control group.

NCT ID: NCT02815813 Completed - Obesity Clinical Trials

Lifestyle Intervention for Young Adults With Serious Mental Illness

Start date: July 3, 2017
Phase: N/A
Study type: Interventional

This is a four year project evaluating the effectiveness of a group-based lifestyle intervention (PeerFIT) supported by mobile health (mHealth) technology and social media compared to Basic Education in fitness and nutrition supported by a wearable Activity Tracking device (BEAT) in achieving clinically significant improvements in weight loss and cardiorespiratory fitness in young adults with serious mental illness (SMI).

NCT ID: NCT02810964 Completed - Schizophrenia Clinical Trials

Sulforaphane to Reduce Symptoms of Schizophrenia

Start date: February 22, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if taking a sulforaphane nutraceutical versus a placebo will reduce symptoms of schizophrenia when used in addition to standard antipsychotic medications.