The Role of Gender in Borderline Personality Disorder

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorUniversity Hospital Heidelberg

About this trial

This study is a mixed-methods, single-arm cross-sectional study comprising 1) a qualitative, exploratory, critical-constructivist content analysis examining the significance of gender in relationship experiences and self-perception among individuals with borderline personality disorder and various gender identities, and 2) a pilot study on the use of the Single-Category Implicit Association Test (SC-IATs, adapted from von Hippel et al., 2018) as preparation for a larger-scale experimental psychological study using the SC-IAT to assess implicit gender- and BPD-related thought processes in people with borderline personality disorder and various gender identities.

15 individuals with BPD and different gender identities will be assessed. The research questions are:

1. What gender-related relationship- and self-experiences can be identified in people with BPD? How do experiences relate to observer-coded and self-reported mentalization ability, as well as self-reported symptoms, experiences of stigmatization, and quality of life? 2. Is there preliminary evidence that Single-Category Implicit Association Tests (SC-IATs) are suitable and reliable instruments for measuring implicit gender- and BPD-related thought processes in people with BPD?

Eligibility criteria

Qualifiers

Signed informed consent form

Individuals of all genders (target: n=5 with female gender identity, n=5 with nonbinary/trans*/gender-non-conforming (TGNC) gender identity, n=5 with male gender identity) between the ages of 18 and 65 at the time of consent

Individuals with a BPD diagnosis made within the last 2 years (ICD-10: F60.3; DSM-5: 301.83, ICD-11: Borderline qualifier)

Understanding of the study procedure, ability and willingness to participate

Disqualifiers

Acute suicidal ideation or acute psychotic symptoms reported by the patient or suspected

Insufficient language skills (i.e., knowledge of German or English)

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

15 Participants
are grouped into 1 trial group

Sponsors and collaborators