borderline personality disorder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The patients in the clinical group are in treatment at GGZ Centraal, a mental health institution. They will be approached through GGZ Centraal. BPD has been determined in these patients with the SCID-5P. The non-clinical group will be approached through the SONA-system of Utrecht University. The patients and healthy individuals will be between 18 and 65 years old.
Exclusion criteria
Exclusion criteria: Exclusion criteria for participants: Participants should not have any problems with their vision. In the non-clinical group, participants with a score above cut-off point on the BSL-23 will be excluded. In the clinical group, participants with acute psychotic symptoms, a neurological disease or being under influence of addictive substances will be excluded.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome measure. - A shift on the questionnaire assessing quality of life between the premeasurement on day 1 and the follow-up measurements on day 7, after one month and after three months. - A shift on the questionnaire mapping perceived social support between the premeasurement on day 1 and the follow-up measurements on day 7, after one month and after three months. | — |
Primary
| Measure | Time frame |
|---|---|
| Primary outcome measures: - Effectiveness of the IBT: the threshold on the continuum from an angry to happy face on day 1 is compared to the threshold measured on day 7 - Effectiveness of the ABT: the mean reaction time for finding the happy face among angry faces within the premeasurement on day 1 is compared to the mean reaction time for finding the happy face among angry faces within the postmeasurement on day 7 | — |
Countries
Netherlands