Actively Recruiting
Mentalization-based Treatment Versus Bona-fide Treatment for Patients With Borderline Personality Disorder in Germany
Led by Heidelberg University · Updated on 2024-05-10
304
Participants Needed
5
Research Sites
213 weeks
Total Duration
On this page
Sponsors
H
Heidelberg University
Lead Sponsor
G
German Research Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
Background: Borderline Personality Disorder (BPD) is a serious mental disorder. Mentalization-based treatment (MBT) is one evidence-based treatment for individuals with BPD. Specifically, MBT has been highlighted for its effectiveness in reduction of suicidal and non-suicidal self-injury (NSSI). Yet, randomized-controlled trials (RCT) on MBT in outpatient settings compared with bona fide treatment (BFT) are still scarce and none has been conducted in Germany. The primary objective of this RCT is to investigate whether outpatient MBT is more effective in the reduction of crisis events (incidences of NSSI and suicide attempts) compared with BFT (namely psychodynamic or cognitive-behavioural psychotherapy) in Germany. Secondary, MBT's efficacy will be investigated with regard to cost-effectiveness, general and interpersonal functioning, BPD and general symptom severity, social adjustment, quality of life, reduction in psychotropic medication and therapy retention. Additionally, moderator as well as common and treatment specific mediator variables will be investigated. Study Design/ Study Population/ Methods: Across 5 study sites in Germany, 304 individuals of all genders from age 18 to 65 with a BPD diagnosis and NSSI or suicide attempts in the past will be asked to participate in the study for two years. In the first year, patients will receive either MBT or BFT (psychodynamic or cognitive behavioural psychotherapy) and will take part in continuous scientific assessments. Scientific assessments will continue after therapy completion up to a 12-moth follow up. As primary outcome, crisis events will be assessed via ecological momentary assessment (EMA) four times a week once per month during the first year and once every three months in the second year. Number of crisis events up to 2 years post randomization will be compared between treatment arms using a log-linear regression model following an intention-to-treat approach. Secondary outcomes, such as borderline and general symptom severity, will be assessed at several timepoints. A within-trial cost-effectiveness analysis (CEA) will be conducted with a societal perspective. Clinical Trial Rationale: This study investigates efficacy of MBT as BPD specific treatment in an outpatient setting compared with BFT in Germany. Results of this study can address a treatment gap in the German healthcare system, and inform about health economic aspects of BPD treatment as well as mechanisms of psychotherapeutic change.
CONDITIONS
Official Title
Mentalization-based Treatment Versus Bona-fide Treatment for Patients With Borderline Personality Disorder in Germany
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Borderline Personality Disorder
- Non-suicidal self-injury or suicide attempts in the past two years, with at least one event in the past six months
You will not qualify if you...
- Acute substance use disorder (except cannabis dependency)
- Diagnosis of schizophrenia or schizotypal personality disorder
- Bipolar I disorder (DSM-5)
- Cognitive impairment (IQ below 80) or organic brain disorder
- Body Mass Index (BMI) below 16.5
- Serious medical condition expected to require hospitalization within the next year
- Insufficient German language skills
AI-Screening
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Trial Site Locations
Total: 5 locations
1
Psychologische Hochschule Berlin
Berlin, Germany
Actively Recruiting
2
Clinic for Psychosomatic Medicine and Psychotherapy, University Hospital Düsseldorf
Düsseldorf, Germany
Not Yet Recruiting
3
Heidelberg University
Heidelberg, Germany, 69115
Actively Recruiting
4
Institute for Psychosocial Medicine, Psychotherapy and Psychooncology
Jena, Germany
Not Yet Recruiting
5
Clinic for Psychosomatic Medicine and Psychotherapy, University Hospital Ulm
Ulm, Germany
Not Yet Recruiting
Research Team
S
Svenja Taubner, Prof.
CONTACT
S
Sophie Hauschild, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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