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NCT07639957
The Role of Gender in Borderline Personality Disorder
Conditions: Borderline Personality Disorder (BPD)
Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Enrollment: 15
Sponsor: University Hospital Heidelberg
Location: Institute for Psychosocial Prevention and Psychotherapy, University Hospital Heidelberg Heidelberg
Summary
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
Inclusion Criteria:
1. Signed informed consent form
2. 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
3. Individuals with a BPD diagnosis made within the last 2 years (ICD-10: F60.3; DSM-5: 301.83, ICD-11: Borderline qualifier)
4. Understanding of the study procedure, ability and willingness to participate
5. The participant is able to read and understand the informed consent form and can provide a written, personally signed, and dated informed consent form.
Exclusion Criteria:
1. Acute suicidal ideation or acute psychotic symptoms reported by the patient or suspected
2. Insufficient language skills (i.e., knowledge of German or English)
Source: ClinicalTrials.gov (NCT07639957). StuddyBuddy aggregates publicly available trial information.