About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Borderline Personality Disorder
non-suicidal self injury or suicide attempts in the past two years as indicated by the IPDE item "repeated suicidal behaviours, gestures, threats or self-harm", one of which has occurred in the past six months
Disqualifiers
acute substance use disorder (exception: cannabis dependency)
diagnosis of schizophrenia or schizotypal personality disorder
bipolar I disorder (DSM-5)
cognitive impairment (IQ<80) or evidence of organic brain disorder
Trial design
Parallel
Treatments tested in this trial
Mentalization-Based Treatment (MBT)
BehavioralPatients in MBT will receive a maximum of 58 sessions in total. Of those, 30 are weekly individual sessions. 28 sessions are weekly group sessions conducted by two therapists, and consisting of 8 introductory sessions of group psychoeducation followed by 20 group therapy sessions. The duration of MBT is 12 months. MBT is manualized and relies on validating the emotional experience of patients that aims to promote mentalizing. The proposed mechanism of change in MBT is to stabilize mentalizing in certain focus areas in order to create a psychic buffer between affect and behaviour to foster affect regulation, reduce impulsivity and promote functional supportive relationships.
Bona-Fide Treatment in Germany (BFT)
BehavioralPatients in BFT will receive one to two weekly sessions of Bona-Fide-Treatment (Psychodynamic Therapy, PT, or Cognitive Behavioural Therapy, CBT) conducted by community experts delivered as short-term psychotherapy (\<24 sessions) or long-term psychotherapy (\>24 sessions). BFT can be delivered as individual, group or a combination of individual and group treatment as stated in the German psychotherapy regulations.
Treatment groups
Trial outcomes
Primary outcomes
change in crisis events assessed with Ecological Momentary Assessment with items based on the SHBQ (Gutierrez et al., 2001)
composite score (non)suicidal self injury
Secondary outcomes
Symptoms of Borderline Personality Disorder assessed with the IPDE (Loranger et al., 1997) and BSL-23 (Wolf et al., 2009)
Change in psychiatric symptom severity assessed with the DASS- 21 (Lovibond & Lovibond, 1995)
Change in health and disability assessed with WHODAS 2.0 Short Form (Üstün et al., 2010)
Change in personality funcitioning assessed with LPFS-BF (Hutsebaut et al., 2016)
Other outcomes
Mentalizing as mediator of change assessed with the Certainty About Mental States Questionnaire (CAMSQ; Müller et al., 2021)
Mediator
Therapeutic Agency Inventory (TAI; Huber et al., 2019)
Mediator
Group Questionnaire - short (GQ; Jensen, 2016)
Mediator
Epistemic Trust, Mistrust and Credulity Questionnaire (ETMCQ; Campbell et al., 2019)
Mediator
Sponsors and contacts
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Heidelberg University
Lead sponsor
German Research Foundation
Collaborator
University Düsseldorf
Collaborator
Jena University Hospital
Collaborator
Universitätsklinikum Ulm
Collaborator
Psychologische Hochschule Berlin
Collaborator