Clinical Trials Logo

Psychotic Disorders clinical trials

View clinical trials related to Psychotic Disorders.

Filter by:

NCT ID: NCT01986517 Completed - Mental Disorders Clinical Trials

Feedback and Psychotherapeutic Competencies

Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of the current study is to examine the influence of feedback on psychotherapeutic competency. The present randomized controlled study compares a feedback condition with a non-feedback condition. Therapists in the feedback condition receive feedback after every fourth session. The feedback is given by two trained and independent raters. The raters are licenced and experienced psychotherapists. Therapists in the non-feedback condition receive no feedback during the psychotherapy.

NCT ID: NCT01981811 Withdrawn - Schizophrenia Clinical Trials

Adherence to Treatment, Safety and Tolerability Study of the Medical Information Device #1 (MIND1) in Subjects With Schizophrenia or Bipolar I Disorder

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate adherence to treatment with, and safety and tolerability of, the medical information device #1 (MIND1) system in subjects with Schizophrenia or Bipolar I Disorder who are currently treated with oral aripiprazole.

NCT ID: NCT01981759 Completed - Schizophrenia Clinical Trials

D-Cycloserine Augmentation of Cognitive Behavioral Therapy for Delusions

Start date: February 2014
Phase: Phase 4
Study type: Interventional

This study is a placebo-controlled 12 week trial of DCS augmentation of once-weekly CBT sessions in 60 schizophrenia subjects with antipsychotic-resistant delusions. In addition to testing efficacy, this trial will characterize DCS effects in terms of time course and persistence of response and will examine DCS effects on memory consolidation and cognitive flexibility as possible mediators of DCS enhancement of CBT for delusions.

NCT ID: NCT01981356 Completed - Psychotic Disorders Clinical Trials

Acceptance and Commitment Therapy for the Inpatient Treatment of Psychosis

ACT-IP
Start date: September 2014
Phase: Phase 0
Study type: Interventional

There is a substantial need for enhancing the efficacy and effectiveness of Veterans Health Administration (VHA) inpatient services for psychosis and tailoring them to support recovery. The proposed pilot study will explore whether Acceptance and Commitment Therapy (ACT), a recovery-oriented, evidence-based inpatient treatment, is a feasible, acceptable, safe, and effective adjunct for the inpatient treatment of Veterans with psychosis at a single VHA site. Additionally, an evaluation of barriers and facilitators to future implementation will be conducted. If promising, the data gained from the proposed study will support future evaluation, implementation and dissemination efforts that have the potential to improve inpatient treatment for psychosis and recovery, and thus, the lives of Veterans, while reducing costs for VHA.

NCT ID: NCT01977521 Recruiting - Clinical trials for Stress Disorders, Post-Traumatic

Transcranial Direct Current Stimulation as Treatment for Auditory Hallucinations

tDCS
Start date: April 2014
Phase: N/A
Study type: Interventional

The present study aims to examine the efficacy of transcranial direct current stimulation on the severity of auditory hallucinations.

NCT ID: NCT01975584 Completed - Schizophrenia Clinical Trials

Neuroendocrine and Immune Response to Stress in Schizophrenia

TSST
Start date: September 2013
Phase: N/A
Study type: Interventional

This is a pilot study. We are testing the physiologic, immune and chemical responses to stress. We believe the results of all measures to stress will be blunted in schizophrenia compared to healthy controls. We will test sex, early life stress and other factors on the relationship to a stress response.

NCT ID: NCT01971307 Completed - Mental Disorders Clinical Trials

Supporting Primary Care in Diagnosis and Choice of Treatment for Patients With Psychosocial Symptoms: SGEPsyScan.

SGE-PsyScan
Start date: December 2013
Phase: N/A
Study type: Interventional

Although effective treatments for psychosocial symptoms and disorders are available, patients frequently do not receive the most appropriate and effective treatment for their symptoms because of inappropriate and unstructured diagnostics of psychosocial symptoms in general practice. The hypothesis is that by using the intervention SGE-PsyScan the clinical symptoms of patients can be assessed more uniformly and earlier as opposed to the GPs' assessment in usual care. As a result, patients are supposed to start earlier with a treatment that fits the type and severity of their symptoms better. The patients will be randomly assigned to either receive the SGE-PsyScan or usual care.

NCT ID: NCT01969500 Completed - Schizophrenia Clinical Trials

Development of a Mobile System for Self-management of Schizophrenia (SOS)

Start date: November 2015
Phase: N/A
Study type: Interventional

This 2-arm clinical trial piloted a mobile Self-Management of Schizophrenia (SOS) system that administers interventions targeting persistent symptoms of psychosis, social dysfunction, and medication adherence. Researchers compared an intervention arm using the SOS system and an arm receiving treatment as usual on the outcomes of change in severity of psychotic symptoms and change in social functioning.

NCT ID: NCT01967420 Completed - Psychosis Clinical Trials

Cognitive Remediation for First Episode of Psychosis Patients

Start date: August 2013
Phase: N/A
Study type: Interventional

This study aims to look at the effectiveness of a combination of cognitive remediation and social cognition training to improve cognition and functioning when compared to cognitive remediation alone. The target population will be those who are experiencing their first episode of psychosis.

NCT ID: NCT01964404 Completed - Schizophrenia Clinical Trials

Cannabis, Schizophrenia and Reward: Self-Medication and Agonist Treatment?

Start date: July 2014
Phase: Phase 1
Study type: Interventional

In this translational research proposal, based on our formulation, we seek to confirm and expand upon data obtained in our pilot study suggesting that cannabis and the cannabinoid agonist dronabinol, given in low dose to patients with schizophrenia and co-occurring cannabis use disorder, will in fact ameliorate the brain reward circuit dysregulation in these patients and, thereby, provide evidence in support of the role of cannabis as a "self-medication" agent for them.