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Personality Disorder, Borderline clinical trials

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NCT ID: NCT05765864 Recruiting - Self-harm Clinical Trials

Self-harm Behaviour Among the Most At-risk Adolescents

SH-MARA
Start date: March 23, 2023
Phase:
Study type: Observational

In the proposed study, three objectives will be pursued: 1. To develop a method to identify more effectively the acute and long-term risk of adolescents with the most threatening self-harm behaviours. 2. To identify the factors that influence the risk of self-harm behaviours and the success of treatment/treatment of these behaviours in the most at-risk adolescents (changes in these factors). 3. Develop guidelines for more effective treatment of the most at-risk adolescents. For this purpose, a sample of approximately 200 young people who will be hospitalised for suicide risk (the most at risk in Slovenia) and an approximately equal number of healthy adolescents will be included. At inclusion, the presence of several factors will be assessed by reviewing demographic data, clinical diagnosis, self-assessment questionnaires and clinical psychological tests (CSSRS, B-NSSI-AT, ISAS, LPFS-BF2.0, BPFSC-11, TSCC, PAI, ECR-RS, DASA-YV, ASHRS), social assessment, and blood sampling for genetic analyses (DNA isolation, sequencing, nucleotide sequence recognition, quantification and evaluation of short tandem repeats, identification of methylation sites). Longitudinal tracking of autoaggressive events and heteroaggressive events during hospitalisation will be performed and recorded on an ongoing basis. The risk and protective factors of the adolescents most at risk will be compared with a control group of adolescents. The same factors will be reassessed in the most at-risk adolescents after 6 and 18 months of treatment as usual. The data will be collected in a data entry and storage system that will ensure the privacy of the data entered in accordance with the GDPR. This will allow the investigators to identify young people at particular risk of severe self-harm behaviour more reliably, to target them for more intensive and effective treatment, and thus to improve their safety, quality of life and prognosis in the short and long term.

NCT ID: NCT04259554 Completed - Depression Clinical Trials

OFC rTMS in Emotionally Unstable and Depressed Patients

ORIENT
Start date: February 14, 2020
Phase: N/A
Study type: Interventional

Treatment of depression with conventional transcranial magnetic stimulation (rTMS) has shown high evidence using high-frequency left dorsolateral prefrontal cortex (DLPFC) stimulation. Recently, it could be demonstrated that treatment of the right orbitofrontal cortex may be effective in patients who did not respond to conventional DLPFC rTMS. Orbitofrontal cortex (OFC) seem to be involved in the etiopathology of emotionally instable personality disorders. Thus, the present one-arm trial is a pilot study investigating if OFC rTMS is feasable, tolerable and effective.

NCT ID: NCT03180541 Completed - Clinical trials for Personality Disorder, Borderline

Evaluating the Coordinated National Implementation of DBT in Ireland

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

This study aims to evaluate the coordinated implementation of Dialectical Behaviour Therapy in Community Mental Health Services in Ireland. There are three main objectives of the current study: - evaluate the effectiveness of DBT for adults and adolescents attending Community Mental Health Services in multiple sites across Ireland - conduct an economic evaluation of the coordinated implementation of DBT in community settings in Ireland - evaluate the implementation initiative by means of quantity, quality and experience of the coordinated implementation

NCT ID: NCT03166579 Completed - Clinical trials for Personality Disorder, Borderline

Effectiveness Evaluation of 'The Endeavour Programme'

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

This study aims to evaluate the effectiveness of Dialectical Behaviour Therapy for adults with Borderline Personality Disorder attending Community Mental Health Services in Cork, Ireland. The main objective of the current study is to determine if completion of a 12 month DBT programme is associated with improved outcomes in terms of borderline symptoms, anxiety, hopelessness, suicidal behaviour, depression and quality of life. A secondary objective includes assessing client progress across multiple time-points throughout the treatment.

NCT ID: NCT03011190 Completed - Clinical trials for Personality Disorder, Borderline

Effectiveness of the Iconic Therapy for Borderline Personality Disorder Symptoms

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

Borderline personality disorder (BPD) is the most prevalent personality disorder in young community population whose most severe complication is suicide. Pharmacotherapy should not be used as the primary treatment for BPD as the benefits are unclear. Psychotherapy is the main treatment for people with BPD and the current recommendation is adapting available comprehensive treatments to develop easier and briefer therapies that are also effective. Iconic Therapy is an innovative option whose good clinical results should be validated on a clinical trial.

NCT ID: NCT00247234 Completed - Clinical trials for Personality Disorder, Borderline

Effectiveness of Group Based Schema Therapy in the Treatment of Personality Disorders

Start date: September 2004
Phase: N/A
Study type: Interventional

This study intends to compare the effectiveness of schema therapy with standard psychiatric outpatient care for patients with borderline or avoidant personality disorder.