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Psychosis clinical trials

View clinical trials related to Psychosis.

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NCT ID: NCT01973270 Completed - Schizophrenia Clinical Trials

Community-Based Cognitive Training in Early Schizophrenia

COTES
Start date: December 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether cognitive training exercises can improve cognitive functioning in young patients with recent-onset schizophrenia, schizoaffective, schizophreniform, and psychosis NOS who are being treated in community mental health settings. We will investigate the effects of web-based cognitive training exercises delivered on a portable laptop computer. The findings will provide us with valuable information on whether cognitive training can improve the cognition and functioning of young individuals early in the course of schizophrenia.

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: NCT01964092 Completed - Depression Clinical Trials

Effect Evaluation of Individual Placement and Support (IPS)

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

Roughly one third of disability pensions issued in Norway are classified as mental and behavioral disorders. The proposed study aims to evaluate the effect of an innovative intervention for returning people with moderate to severe mental health disorders to work: Individual Placement and Support (IPS).

NCT ID: NCT01924039 Terminated - Psychosis Clinical Trials

Brief Motivational Enhancement Therapy for Concurrent Disorders

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

The investigators are proposing a project that will examine the effectiveness of brief motivational enhancement therapy in a population with concurrent psychotic disorders and substance use disorders. This study will represent an emerging line of inquiry, as best practice interventions with this concurrent disordered (CD) populations are yet to be established.

NCT ID: NCT01907282 Completed - Psychosis Clinical Trials

Prevention Trial of Family Focused Treatment in Youth at Risk for Psychosis

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

Preventing psychotic disorders such as schizophrenia and associated functional disability could relieve an enormous burden of personal and family suffering and economic losses to society. This project aims to conduct a pilot randomized trial to determine the efficacy of a family-focused treatment in comparison with treatment-as-usual in enhancing functional outcomes, stabilizing symptoms, and preventing or delaying the onset of full psychosis in transitional age youth with prodromal symptoms. The results of this study will be crucial for the development of cost-effective, evidence-based psychosocial approaches to psychosis prevention and thus will have major implications for public health.

NCT ID: NCT01903707 Recruiting - Schizophrenia Clinical Trials

Cognitive Remediation in Schizophrenia

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

The aim of this project is to undertake a randomized placebo controlled trial of cognitive remediation therapy (CRT) that focuses on working memory training in a sample of community based patients with chronic schizophrenia or other psychoses. Cognitive deficits are a problem for many people with schizophrenia. This study will use computerized cognitive remediation training (which the participant can carry out at home) over a period of a few months.

NCT ID: NCT01793220 Unknown status - Psychosis Clinical Trials

Economic and Clinical Outcomes of Attendance in Psychosis Services Using SMS.

ECO APSS
Start date: March 2013
Phase: N/A
Study type: Interventional

The aim of this research is to find out if mobile phone text message reminders of appointments can help to address missed appointments in Psychosis Community Services. Another aim is to examine if fewer missed appointments result in clinical benefits for service users and in lower costs for Psychosis Community Services over a period of 6 months. 600 users from 2 London Psychosis Community Services will take part in this research. Each participant will be put into one of two groups, as s/he joins the study: In the first (experimental) group, each participant will receive appointment reminders for 6 months (7 and 1 day/s before each appointment), starting with the first available opportunity upon joining the study. In the second (control) group, each participant will not receive appointment reminders for 6 months. The choice of group for each individual will be made at random by a computer. Clinical information will be collected for 6 months from the time each participant joins the study, using, with his or her consent, their anonymised electronic medical records. The following clinical information will be compared between the experimental and control groups: Attendance of appointments, number of inpatient admissions, number of days in inpatient care, number of inpatient admissions under the mental health treatment act, number of referrals to a home treatment team, number of times patient has changed medication, health and social functioning. Service use, service costs and the cost-effectiveness of the reminder system will also be examined. Towards the end of their participation, service users, as well as mental health professionals, will be invited to express their views, concerns and suggestions in relation to the reminder service by completing a brief anonymised (service users) or anonymous (staff) questionnaire

NCT ID: NCT01783457 Completed - Psychosis Clinical Trials

e-Learning & Development of an Evidence-based Psychoeducational Programme for First Episode Psychosis

Start date: January 2011
Phase: N/A
Study type: Interventional

Treatment delay in psychosis usually lead to slower recovery, an increase in associated comorbidity and greater deterioration in social and family life of patients. Previous studies indicate that an early intervention with guidelines for increasing adherence to treatment, disease awareness and condition management leads to better progression of the disorder and is therefore related to a better prognosis. Several studies have found that the rate of relapse is higher in patients with pharmacological treatment alone compared to those also receiving psychoeducation, who tend to improve their adherence to treatment and reduce toxic drugs dosage. Hypotheses: - Individual psychoeducation will be effective as complementary therapy to pharmacological treatment in patients with a first psychotic episode, improving disease evolution. - BDNF levels will increase more in the patients receiving individual therapy compared to those without it. - Psychoeducation can be performed similarly in all participating centers if the therapists receive the same training and use the same psychoeducation material. - The use of telemedicine for the follow-up of the patients will help improve the welfare work and therefore the disease evolution.

NCT ID: NCT01781364 Completed - Psychosis Clinical Trials

Neuroplasticity-oriented Cognitive Intervention in Early Onset and First Admission Schizophrenia

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to reveal the specific effects of computer-aided cognitive training on course and rehabilitation in early onset schizophrenia

NCT ID: NCT01768000 Completed - Psychosis Clinical Trials

The Family Cognitive Adaptation Training Manual: A Test of Effectiveness

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

The purpose of this study is to examine the effectiveness of family cognitive adaptation training, including its impact on functioning and caregiver burden. Families that receive the manual will be compared with a control group of families that will not receive the manual. The larger goal is to add to the tools family members have access to better support their family members with schizophrenia.