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Personality Disorders clinical trials

View clinical trials related to Personality Disorders.

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NCT ID: NCT02507206 Completed - Clinical trials for Schizotypal Personality Disorder

A D1 Agonist For Working Memory

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of the study is to examine the effects of the administration of a drug called DAR-0100A on attention and memory in persons with schizotypal personality disorder (SPD). DAR-0100A has not been FDA approved, however in recent studies has been used to treat cognitive deficits, meaning problems in the way you organize your thinking, in people diagnosed with schizophrenia. Many people who carry a diagnosis of schizotypal personality disorder have trouble with attention and memory. Increasing the presence of a brain chemical called dopamine has been found to help people with schizophrenia with their attention and memory problems. This study will investigate whether the same is true for people with schizotypal personality disorder by using DAR-0100A, a drug that has been shown to help with the cognitive deficits of people with Parkinson's disease by increasing dopamine effects. Information collected in this experiment may lead to a better understanding of the brain mechanisms involved in schizotypal personality disorder and improve treatments for the psychological problems associated with this condition.

NCT ID: NCT02465697 Completed - Clinical trials for Borderline Personality Disorders

Changes in the Brain as Borderline Patients Learn to Regulate Their Emotions

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

Borderline Personality Disorder (BPD), a prevalent psychiatric disorder found in approximately 2% to 6% of the population and 20% of hospitalized psychiatric patients, has proven quite treatment resistant. This study is designed to determine whether patients with BPD can be trained to improve their ability to regulate their emotions and whether this leads to changes in how their brans regulate emotion.

NCT ID: NCT02397187 Not yet recruiting - Clinical trials for Personality Disorders

Efficacy of a Structured, Dimension-based, STI in De-compensated Personality-disorder, Hospitalized, Patients

LOOP-PersDis
Start date: March 2015
Phase: N/A
Study type: Interventional

The assessment of the efficacy of a structured, dimension-based, STI (Short Term Intervention) in de-compensated Personality-disorder, hospitalized, patients

NCT ID: NCT02397031 Completed - Clinical trials for Borderline Personality Disorder

Mindfulness and Interpersonal Effectiveness Skills in Borderline Personality Disorder

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

The purpose of the study was to determine whether mindfulness training could be more effective than another active intervention in reducing borderline personality disorder (BPD) symptoms. The main hypothesis was that patients allocated to the mindfulness group would show a greater improvement on global BPD symptomatology. As a second objective, we explored some of the possible underlying mechanisms of both active treatments. For that purpose, changes in decentering, mindfulness facets and cognitive processing of social interactions were also evaluated.

NCT ID: NCT02387736 Active, not recruiting - Clinical trials for Borderline Personality Disorder

DBT for Chronically Self-harming Individuals With BPD: Evaluating the Clinical & Cost Effectiveness of a 6 mo. Treatment

FASTER-DBT
Start date: February 2015
Phase: N/A
Study type: Interventional

Standard one-year dialectical behaviour therapy (DBT), which has four components, is an effective treatment for people with borderline personality disorder. However, such DBT programs are in short supply and costly, resulting in long wait lists. In practice, DBT is often reduced in length or intensity. This study will determine whether shorter DBT treatment is clinically effective and cost-effective. In total, 240 self-harming BPD patients will be randomly assigned to receive either 1 year or 6 months of DBT, with follow-up lasting two years. Rates of suicidal and self-harm behaviours, use of health care and general psychological functioning will be examined.

NCT ID: NCT02370316 Completed - Clinical trials for Borderline Personality Disorder

Biomarkers of Change in BPD After Metacognitive Interpersonal Therapy-standard Approach

CLIMAMITHE
Start date: December 2015
Phase: N/A
Study type: Interventional

The present randomised clinical trial aims to assess the clinical and neurobiological changes following Metacognitive Interpersonal Therapy -standard approach (MIT-SA) compared with Clinical Structured Treatment (CST) derived from specific recommendations in APA guidelines for borderline personality disorder (BPD). The investigators will assess clinical changes in metacognitive abilities and in emotion regulation and changes in brain activation patterns at the resting state and while they view emotional pictures. A multidimensional assessment will be performed at the baseline, at 6, 12, 18 months. The investigators will take structural and functional Magnetic Resonance Images (MRIs) in MIT-Treated BPD (N=30) and CST-treated BPD (N=30) at baseline and after treatment, as well as a group of 30 healthy and unrelated volunteers that will be scanned once for comparison. Furthermore, blood analyses will be done in order to assess level of BDNF and some hormone levels (oxytocin and vasopressin) before and after treatments.

NCT ID: NCT02330614 Completed - Personality Clinical Trials

Personality Bleaching

NEOFFI
Start date: July 2013
Phase: N/A
Study type: Observational

128 patients between 18 and 76 years who attended the Operative Dentistry Clinic at Dental School, Universidad de Chile, were included in the study. 58 patients were bleaching (experimental group) and 70 patients don't accepted the bleaching procedure (control group) were included in this study and signed a consent form.Experimental group Patients who agreed to be bleaching were treated with 10% carbamide peroxide (CP) gel (Whiteness Perfect, FGM) to each subject With verbal instructions for 3 weeks with daily applications of 1 hour according to manufacturers indications , before and after this procedure was applied again the NEO-FFI personality test form, had 30 minutes to answer it.Control group:Patients who refused to be bleached were administered the personality test NEO-FFI, had 30 minutes to answer it.

NCT ID: NCT02308462 Completed - Clinical trials for Substance-Related Disorders

Implementation and Evaluation of a Family-based Intervention Program for Children of Mentally Ill Parents

CHIMPs
Start date: November 2014
Phase: N/A
Study type: Interventional

In order to identify psychological stress in children and adolescents of mentally ill parents as early as possible, a special intervention program (CHIMPs = Children of mentally ill parents) was developed. The study at hand will implement this intervention program at five sites in Germany and will further evaluate its effectiveness. The CHIMPs intervention is assumed to reduce children's psychopathology and enhance their health related quality of life.

NCT ID: NCT02276469 Completed - Bipolar Disorder Clinical Trials

Peer Support for Severe Mental Disorders

PEER
Start date: July 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine wether peer support is effective for the treatment of people with severe mental illness.

NCT ID: NCT02273674 Completed - Clinical trials for Borderline Personality Disorder

TMS in Borderline Personality Disorder Patients

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the potential effects of repetitive transcranial magnetic stimulation in the improvement of neuropsychological deficits and symptomatology in borderline personality disorder patients. Specially in cognitive flexibility, inhibition control and social cognition.