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Mechanisms of Change in Brief Treatment for Borderline Personality Disorder

Mechanisms of Change in Brief Treatment for Borderline Personality Disorder: A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03717818
Acronym
BPDCHANGE
Enrollment
80
Registered
2018-10-24
Start date
2018-10-19
Completion date
2022-12-31
Last updated
2018-10-25

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

Conditions

Borderline Personality Disorder

Brief summary

The present two-arm randomized controlled study aims at testing the effects (i.e., symptom reduction) and the underlying mechanisms of change associated with a brief psychiatric treatment (10 sessions over 4 months), compared with treatment as usual. Participants undergo assessments at four points (intake, 2 months, discharge and 12 month follow-up). In addition to symptom measures, all individuals undergo a two-step assessment for the potential mechanisms of change (i.e., emotion and socio-cognitive processing): a) behavioural and b) neurofunctional. We hypothesize that change in the mechanisms explains the treatment effects. The present study uses an innovative treatment of BPD and at the same time a sophisticated assessment procedure to demonstrate the critical role of psychobiological change in emotion and sociocognitive processing in brief treatments. It will help increase the effectiveness of initial treatment phase for BPD and help diminish the societal burden of disease related with BPD. This study is funded by the Swiss National Science Foundation (SNSF).

Interventions

BEHAVIORALGood Psychiatric Management - Brief

specific interventions as defined by Gunderson and Links (2014)

BEHAVIORALtreatment as usual

non-specific intervention

Sponsors

University of Lausanne Hospitals
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Borderline Personality Disorder * age between 18 and 35

Exclusion criteria

* non-mastery in French * neurological disorders * schizophrenia (according to DSM-5)

Design outcomes

Primary

MeasureTime frameDescription
ZAN-BPD (Zanarini Borderline Personality Disorder Scale; Zanarini, 2003)4 monthsmeasures borderline symptomatology from an dimensional perspective, ranges between 0 and 36 (36 being the most symptomatic), global score (sum of all 9 items coded between 0 and 4) used.

Secondary

MeasureTime frameDescription
OQ-45 (Outcome Questionnaire-45.2, Lambert et al., 2004)4 monthsmeasures the level of problems (distress, social and interpersonal) on a scale ranging from 0 to 180 (45 items coded between 0 and 4, 4 being the most symptomatic). A total sum score will be used
BSL-23 (Borderline Symptom List, Short Version; Bohus et al., 2009)4 monthsmeasures the intensity of borderline symptoms using a mean score of the 23 items ranging between 0 and 4 (4 being the most symptomatic), the mean score will be used.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026