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Personality Disorders clinical trials

View clinical trials related to Personality Disorders.

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NCT ID: NCT00204347 Completed - Clinical trials for Borderline Personality Disorder

Effective Measurement of Risperidone Treatment Outcome for Persons With Borderline Personality Disorder

Start date: July 2003
Phase: Phase 4
Study type: Interventional

The objective of Study A is to evaluate the efficacy of risperidone on the 4 behavioral dimensions of Berderline Personality Disorder (BPD)in an open label trial:mood swings, impulsivity, thing difficulties and disturbed relationships. The secondary objective of this study (Study B)is to validate a self-report measure of clinical symptoms specific to the treatment of patients with BPD, the UAB Borderline Rating Scale(BRS).

NCT ID: NCT00202215 Completed - Eating Disorders Clinical Trials

Chrysalis Day Program Body Mass Index Study

Start date: October 2001
Phase: N/A
Study type: Interventional

This is a study to determine if the approach taken to treat patients in the Chrysalis Day Hospital Program will favourably effect their health status as assessed by Body Mass Index (BMI)

NCT ID: NCT00202202 Completed - Clinical trials for Borderline Personality Disorder

User Satisfaction Survey - Personality Disorder Service

Start date: November 2002
Phase: N/A
Study type: Interventional

Can we improve our community partners satisfaction with a change in how psychiatric consultations are delivered to their clients by our psychiatrist? This survey of users of the service will compare the level of satisfaction before(retrospectively) to after the way the service is provided is changed.

NCT ID: NCT00184418 Completed - Schizophrenia Clinical Trials

The Immune System and Psychiatric Disorders

Start date: January 2005
Phase: N/A
Study type: Observational

The study is based on a hypothesis that there is interaction between the activity in the immune system and in the mind. To study this, the investigators register different measures for activity in the immune system on patients unselectedly admitted to an acute psychiatric ward. The psychiatric statuses and diagnoses of these patients are carefully defined as well.

NCT ID: NCT00184301 Completed - Anorexia Nervosa Clinical Trials

A Comparison Study of Treatments Given to Patients With Concurrent Eating Disorder and Personality Disorder.

Start date: September 2005
Phase: N/A
Study type: Interventional

The aim of this study is to determine whether in-patient treatment is better then intensive out-patient group treatment for patients with concurrent eating disorder and personality disorder.

NCT ID: NCT00183651 Completed - Suicide Clinical Trials

Treatment of Suicidal Women With Borderline Personality Disorder

Start date: April 2004
Phase: Phase 2
Study type: Interventional

This study is a component analysis of dialectical behavior therapy (DBT) to determine the importance of DBT skills training and DBT individual therapy in treating suicidal women with borderline personality disorder.

NCT ID: NCT00178061 Completed - Clinical trials for Borderline Personality Disorder

Effects of Comorbid Personality Disorder on the Treatment of Bipolar I Disorder

Start date: August 1997
Phase: Phase 4
Study type: Interventional

This study will examine the impact of comorbid personality disorder on the outcome of treatment among patients with bipolar I disorder.

NCT ID: NCT00158028 Completed - Clinical trials for Schizotypal Personality Disorder

Risperidone in the Treatment of Psychotic-like and Deficit Symptoms of Schizotypal Personality Disorder

Start date: November 1995
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the efficacy of risperidone compared to placebo in the treatment of the psychotic-like and deficit symptoms of schizotypal personality disorder (SPD). Treatment with risperidone, a 5HT2 and dopamine D2 blocking agent, holds particular promise in the treatment of SPD. Unlike traditional antipsychotics, risperidone targets the deficit or negative symptoms of schizophrenia. The deficit-like symptoms of SPD are therefore also likely respond to treatment with risperidone. One common complication in the present psychopharmacologic treatment of SPD with traditional neuroleptics is the fact that many patients discontinue treatment due to the medication-induced dysphoria. Given initial reports and the serotonergic component of the risperidone mechanism, risperidone is anticipated to produce little or no dysphoria.

NCT ID: NCT00154154 Completed - Clinical trials for Borderline Personality Disorder

Hope for the Chronically Suicidal Patient

Start date: October 2002
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the clinical and cost effectiveness of Dialectical Behavior Therapy (DBT) for chronically suicidal behavior in individuals diagnosed with borderline personality disorder (BPD). Recent investigations of DBT have yielded positive results and have challenged the widely held opinion that the prognosis for this condition is poor. This study will consist of a two-arm randomized controlled trial that will compare DBT with a General Psychiatric Management (GPM) condition consisting of a structured algorithmic medication intervention plus psychosocial counseling. One-hundred and eighty participants will be randomly assigned to either DBT or to the GPM condition. Clinical outcomes will be assessed by changes in: (1) parasuicidal behaviour; (2) treatment retention; (3) psychiatric symptomatology; (4) anger expression; (5) social functioning and (6) health status. Cost outcomes will include an analysis of health service utilization. Clinical and cost evaluations will occur at 4-month intervals over the course of the one-year treatment and over a two-year follow-up.

NCT ID: NCT00153959 Completed - Schizophrenia Clinical Trials

Psychiatric Day Hospital Treatment

Start date: n/a
Phase: N/A
Study type: Interventional

The aim of the study was to compare the effectiveness of acute psychiatric day care to conventional inpatient care within a cross-national multi-site randomised controlled trial.