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PRO*BPD: Effectiveness of outpatient treatment PROgrammes for Borderline Personality Disorder: A comparison of Schema Therapy and Dialectical Behaviour Therapy

PRO*BPD: Effectiveness of outpatient treatment PROgrammes for Borderline Personality Disorder: A comparison of Schema Therapy and Dialectical Behaviour Therapy - PROBPD

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011534
Enrollment
128
Registered
2017-01-11
Start date
2014-11-26
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

F60.31

Interventions

Group 1: Intensive outpatient treatment program of ST with one individual and one group session per week for 1.5 years Group 2: Intensive outpatient treatment program of DBTwith one individual and one

Sponsors

Klinik für Psychiatrie und Psychotherapie, Universität zu Lübeck
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Primary DSM-IV diagnosis of BPD (diagnosed by SCID-II interview) Severity of BPD > 20 points in the BPDSI interview (this is a empirically derived severity criterion, distinguishing BPD pathology from other PD-pathology) Willingness to participate in the study (informed consent) Willingness and ability to remain for 1.5 years in the study and to participate reliably in therapy (no relocation plans etc.)

Exclusion criteria

Exclusion criteria: Major psychotic disorder (lifetime diagnosis Intellectual deficits (IQ<85) Inadequate German language skills Acute serious substance dependencies (DSM-IV) that cause severe cognitive restrictions during therapy and which calls for detoxification treatment. Participation is possible after detox treatment and a four weeks abstinence period.

Design outcomes

Primary

MeasureTime frame
Change in BPD symptom severity assessed with the mean score of the Borderline-Personality Disorder Severity Index at 1 year follow up.

Secondary

MeasureTime frame
Change in quality of life measured with EQ-5D and WHOQoL, social functioning and participation measured with GAF-SOFAS, Cost-effectiveness measured with a COST-Interview, comorbidity (SKID I and II), general psychiatric symptoms (BSI, QIDS), other measures of BPD-psychopathology (dissociation, emotion regulation skills, experiential avoidance) at one year follow-up.

Countries

Germany

Contacts

Public ContactEva Faßbinder

Klinik für Psychiatrie und Psychotherapie, Universität zu Lübeck

eva.fassbinder@uksh.de0451-50098702

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 5, 2026