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The Short-Term MBT Project

Short-term Versus Long-term Mentalization-based Therapy for Outpatients With Subthreshold or Diagnosed Borderline Personality Disorder: a Randomized Clinical Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03677037
Acronym
MBT-RCT
Enrollment
166
Registered
2018-09-19
Start date
2018-09-24
Completion date
2023-12-15
Last updated
2024-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Borderline Personality Disorder

Keywords

mentalization-based therapy, borderline personality disorder, randomized clinical trial, psychotherapy research, treatment intensity

Brief summary

The study will evaluate the benefitial and harmful effects of short-term (20 weeks) compared to long-term (14 months) mentalization-based therapy for outpatients with subthreshold or diagnosed borderline personality disorder.

Detailed description

Psychotherapy for borderline personality disorder is often lengthy and resource-intensive. Mentalization-based therapy is an example of an evidence-based treatment that currently has empirical support as an 18-months outpatient program for borderline personality disorder. However, this duration is rarely available, and the long and costly treatment combined with a highly prevalent disorder result in insufficient access to evidence-based care. The trial is an investigator-initiated, single-centre, assessor-blinded, randomized clinical superiority trial of short-term (20 weeks) compared to long-term (14 months) outpatient mentalization-based therapy for borderline personality disorder or subthreshold borderline personality disorder. Participants will be recruited from the Outpatient Clinic for Personality Disorders at Stolpegaard Psychotherapy Centre, Mental Health Services, Capital Region of Denmark. Participants will be assessed at trial intake using the Mini International Neuropsychiatric Interview and the Structured Clinical Interview for DSM-5 Personality Disorders. Participants will be included if they meet a minimum of four DSM-5 criteria for borderline personality disorder. Participants will be assessed blind to treatment allocation at baseline, and at 8, 16, and 24 months after randomization. The primary outcome is severity of borderline symptomatology assessed using the Zanarini Rating Scale for Borderline Personality Disorder interview. Secondary outcomes include self-harm incidents, functional impairment (Work and Social Adjustment Scale), quality of life (Short-Form Health Survey), and global functioning (Global Assessment of Functioning scale). Psychiatric symptoms (Symptom Checklist 90) will be included as an exploratory outcome. Measures of personality functioning, attachment, group alliance, borderline symptoms and mentalization skills will be included as predictor and mediator variables.

Interventions

OTHERShort-term MBT

Short-term mentalization-based therapy

OTHERLong-term MBT

Long-term mentalization-based therapy

Sponsors

University of Copenhagen
CollaboratorOTHER
Copenhagen Trial Unit, Center for Clinical Intervention Research
CollaboratorOTHER
Mental Health Services in the Capital Region, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

exclusive to the Outpatient Clinic * Age \>18 years * Personality disorder(s) considered to be primary diagnosis/diagnoses Inclusion Criteria exclusive to the trial: * A minimum of four DSM-5 criteria for borderline personality disorder * Written informed consent

Exclusion criteria

exclusive to the Outpatient Clinic: * Possibility of a learning disability (IQ\<75) * A diagnosis of schizotypal personality disorder or antisocial personality disorder * Presence of a comorbid psychiatric disorder that requires specialist treatment elsewhere * Current (past 2 months) substance dependance including alcohol * Concurrent psychotherapeutic treatment outside the clinic

Design outcomes

Primary

MeasureTime frameDescription
Change in severity of borderline personality disorder assessed with the Zanarini Rating Scale for Borderline Personality Disorder (ZAN-BPD) interviewAssessed at baseline, and at 8, 16 and 24 months post-randomizationZAN-BPD is an investigator-administered interview assessing change in severity of borderline personality disorder over time. Each of the nine DSM-5 criteria for borderline personality disorder are rated on a scale from 0-4, where 4 is the most severe, yielding a total score from 0-36.

Secondary

MeasureTime frameDescription
Change in functional impairmment assessed with the Work and Social Adjustment Scale (WSAS)Assessed at baseline, and at 8, 16 and 24 months post-randomizationWSAS is a 5-item questionnaire assessing change in functional impairment. Each item is rated on a scale from 0-8, where 0 is no impairment and 8 is severe impairment, yielding a total score between 0-40.
Change in quality of life assessed with the Short-Form Health Survey 36 (SF-36)Assessed at baseline, and at 8, 16 and 24 months post-randomizationSF-36 is a questionnaire assessing change in self-reported quality of life over time. The instrument measures eight health dimensions: physical function (PF), role physical (RF), bodily pain (BP), social function (SF) role emotional (RE), general health (GH), vitality (VT) and mental health (MH). The questions related to each dimension are scored on a scale from 0 (worst score) to 100 (best score).
Change in global functioning assessed with the Global Assessment of Functioning (GAF)Assessed at baseline, and at 8, 16 and 24 months post-randomizationGAF is an investigator-administered rating of change in global functioning over time. Global funtioning is rated on a scale from 0-100 for both symptomatic and functional impairment, yielding two total scores from 0-100, where 100 is no impaitment and 0 is severe impairment.
Change in amount of self-harm incidentsAssessed at baseline, and at 8, 16 and 24 months post-randomizationProportion of participants with severe self-harm defined as deliberate acts of self-harm resulting in visible tissue damage - data will be collected as both dichotomous data and count data.

Other

MeasureTime frameDescription
Change in psychiatric symptom distress assessed with the Symptom Checklist 90 (SCL-90)Assessed at baseline, and at 8, 16 and 24 months post-randomizationSCL-90 is a questionnaire assessing change in psychiatric symptom distress over time. All 90 items are rated on a scale from 0-4. The total score is divided by number of items, yielding a total score on the Global Severity Index ranging from 0 to 4, where 4 is the most severe.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 1, 2026