Feasibility of Priovi, an e-health tool based on schema therapy to treat patients with Borderline Personaility Disorder, as support to face-to-face psychotherapy - a qualitative case study

Feasibility of Priovi, an e-health tool based on schema therapy to treat patients with Borderline Personaility Disorder, as support to face-to-face psychotherapy - a qualitative case study - Priovi

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

DRKS

Registry ID

DRKS00011538

Enrollment

Registered

2017-01-03

Start date

2014-07-01

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: Psychotherapy programm including one individual Face-toface-ST session per week in combination with priovi, an e-health tool based on schematherapy for patients with BPD (recommended use: ca.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

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)

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.

Design outcomes

Primary

Measure	Time frame
Assessment of patients' subjective experiences with the e-health tool priovi by means of a semi-structured qualitative interview through the whole course of therapy	—

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: Feb 23, 2026