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Personality Disorders clinical trials

View clinical trials related to Personality Disorders.

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NCT ID: NCT03602521 Completed - Clinical trials for Borderline Personality Disorder

Reactivity of Patients With Borderline Personality Disorder to an Ecological Interpersonal Stress

ROI
Start date: February 27, 2019
Phase: N/A
Study type: Interventional

Use lay language. According to the World Health Organization 1 death by suicide occurs every 40 seconds, leading suicide prevention to one of the public health priority. BPD (Borderline Personality Disorder) is a common condition affecting 6% of the population. This disorder is characterized by unstable emotions, unstable mood, difficulties with relationship and feer of abandonment. Borderline Personality Disorder is also the psychopathology the most related to suicidal attempts. Indeed, up to 50% of the patients admitted to hospital after a suicide attempt are diagnosis with a Borderline Personality Disorder Negative interpersonal events (events occurring between two people) are known as the main stressor that trigger a suicidal attempt. People with a Borderline Personality Disorder are highly sensitive to it. Moreover, neuropeptides such as oxytocin (OXT), vasopressin and opioid are known to be involved in the regulation of the emotions, especially those linked to relationship. The purpose of this study is to improve knowledge in suicidal behaviors. After simulating an interpersonal stress, the evolution of plasma neuropeptides level (OXT, vasopressin and opioid) of patients with a BPD will be compared to healthy controls (HC). Clinical data reflecting how the participant is feeling will be collected as well.

NCT ID: NCT03519035 Not yet recruiting - Clinical trials for Borderline Personality Disorder

Study of Hallucinations in Patients With Borderline Personality Disorder

Start date: July 2018
Phase:
Study type: Observational [Patient Registry]

Hallucinations in borderline personality disorder are a frequent an serious trouble which have an important impact in patients lives. Despite this, they are often ignored by nursing staff, and are not an important criteria in Diagnostic and Statistical Manual (DSM) 5 and Classification Internationale des maladies (CIM-10). The main objective of our study is to assess the prevalence of this trouble in borderline personality disorder (BPD) population, and to characterize the hallucinations in order to compare our results with those of international studies.

NCT ID: NCT03498937 Not yet recruiting - Clinical trials for Borderline Personality Disorder

Effects of tDCS on Impulsiveness Among People Suffering From Borderline Personality Disorder

TIMBER
Start date: May 2019
Phase: N/A
Study type: Interventional

The study aims to evaluate the impact of transcranial direct current stimulation (tDCS) on impulsiveness of adults suffering from Borderline Personality Disorder. Short- and long-term effects are assessed by electroencephalography (EEG) records, experimental tasks and self-rated scales.

NCT ID: NCT03495375 Completed - ADHD Clinical Trials

Treating Impulsivity in Adults With Probiotics

PROBIA
Start date: February 22, 2019
Phase: N/A
Study type: Interventional

A multicentre randomized double-blind placebo controlled parallel design (10 weeks) study investigating probiotic supplementation in highly impulsive adults (18-65 yrs; N=180). The probiotic studied is Synbiotic2000Forte that contain three well-studied anti-inflammatory lactic acid bacteria (LABs) and four fermentable fibers: Pediococcus pentosaceus 5-33:3, Lactobacillus paracasei subsp paracasei 19, and Lactobacillus plantarum 2362 in combination with the following four fermentable fibres: betaglucan, inulin, pectin and resistant starch. With this study we aim to detect, whether treatment with probiotics is effective in adults with high levels of impulsivity, compulsivity, and aggression.

NCT ID: NCT03472638 Active, not recruiting - Major Depression Clinical Trials

Dorsomedial rTMS For Depression In Borderline Personality Disorder

rTMS
Start date: July 2016
Phase: N/A
Study type: Interventional

This randomized trial with a crossover design will examine the efficacy of rTMS targeting the dorsomedial prefrontal cortex as a treatment for medication-resistant major depression in patients meeting diagnostic criteria for borderline personality disorder.

NCT ID: NCT03434457 Completed - Infant Development Clinical Trials

Maternal Adversity, Vulnerability and Neurodevelopment

MAVAN
Start date: October 1, 2003
Phase:
Study type: Observational

Maternal Adversity Vulnerability and Neurodevelopment (MAVAN) project is a prospective community-based, pregnancy and birth cohort of Canadian mother-child dyads. The main objective of MAVAN project is to examine the pre- and postnatal influences, and their interaction, in determining individual differences in children development. The MAVAN project is designed to examine the consequences of fetal adversity as a function of the quality of the postnatal environment, focusing on mother-infant interactions.

NCT ID: NCT03418675 Completed - Clinical trials for Borderline Personality Disorder

Brexpiprazole in Borderline Personality Disorder

Start date: November 26, 2018
Phase: Phase 2
Study type: Interventional

The primary objective of the proposed study is to evaluate the safety and efficacy of Brexpiprazole in adults with borderline personality disorder (BPD). The hypothesis to be tested is that brexpiprazole will be more effective and well tolerated in adults with BPD compared to placebo. The proposed study will provide needed data on the treatment of a disabling disorder.

NCT ID: NCT03418142 Completed - Clinical trials for Borderline Personality Disorder

Evaluating an Internet-Based Self-Management Intervention for Borderline

REVISIT
Start date: January 29, 2018
Phase: N/A
Study type: Interventional

The trial aims to evaluate the effectiveness of a novel internet intervention (Priovi), which was designed to introduce relevant schema therapy techniques to Persons with Borderline Personality Disorder (BPD). Therefore, 200 people with BPD will be recruited and randomized to two groups: (1) a control group, in which they may engage with any BPD treatment (Care-as-Usual, CAU) and receive access to Priovi after a delay of 12 months (i.e., CAU/wait list control group), or (2) to a treatment group that immediately receives 12-month access to Priovi and may also use CAU. The primary outcome measure is the score of the Borderline Personality Disorder Severity Index (BPDSI), collected at three, six and 12 month post-baseline.

NCT ID: NCT03408860 Completed - Clinical trials for Borderline Personality Disorder

Isolating Mechanisms in the Treatment of Borderline Personality Disorder

Start date: October 15, 2017
Phase: N/A
Study type: Interventional

Borderline personality disorder (BPD) is a commonly occurring, severe, and costly condition that interferes greatly with quality of life. Considerable comorbidity with other disorders and existing multicomponent treatments with largely untested putative mechanisms of action represent obstacles for effective dissemination of BPD treatment; in light of this gap, the purpose of the present study is to isolate the effects of individual treatment components on putative mechanisms implicated in both BPD. This study will answer important theoretical questions about the mechanism of treatment change, and might lead to more efficacious, cost-effective, and easily disseminable treatment strategies for BPD, a severe and understudied disorder.

NCT ID: NCT03407443 Withdrawn - Clinical trials for Help-Seeking Behavior

Pilot the Use of VA Make the Connection Campaign to Facilitate Help Seeking Among Vulnerable Veterans

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

This pilot study seeks to determine if exposure to the Make the Connection campaign messages developed by the U.S. Department of Veterans Affairs (VA) is associated with changes in mental-health related outcomes, specifically: (1) psychosocial determinants that drive help seeking behaviors (knowledge, attitudes and intentions); and (2) perceived barriers to seeking care. Participants are randomly assigned to message exposure or control (no exposure) conditions. Data from this project will inform mental health education and outreach efforts targeted towards Veterans experiencing mental health concerns.