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Differences in clinical characteristics between post-traumatic stress disorder (PTSD, ICD-11), complex post-traumatic stress disorder (cPTSD, ICD-11) and borderline personality disorder (BPD)

Differences in clinical characteristics between post-traumatic stress disorder (PTSD, ICD-11), complex post-traumatic stress disorder (cPTSD, ICD-11) and borderline personality disorder (BPD)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00032754
Enrollment
300
Registered
2023-10-24
Start date
2023-11-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Study no. 1: ICD-10 (F43.1, F60.31) and ICD-11 (6B40, 6B41, 6D10, 6D11.5) Study no. 2 (completed): ICD-11 6B40 (posttraumatic stress disorder) and 6B41 (complex posttraumatic stress dirsorder)) F43.1 F60.31

Interventions

Group 1: Patients with diagnosis of PTSD and/or BPD are asked once about their subjective level of suffering, symptom frequency, psychiatric comorbidities (anxiety and depression), type and frequency

Sponsors

Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Göttingen (UMG)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Study no. 1: outpatient or (partially) inpatient patients of the clinic for Psychiatry and Psychotherapy at the Universitätsmedizin Göttingen (UMG) who currently have a supsected or confirmed diagnosis of PTSD (ICD-10: F43.1) and/or borderline personality disorder (ICD-10: F60.31). Study no. 2 (completed): outpatient patients of the clinic for Psychiatry and Psychotherapy at the Universitätsmedizin Göttingen (UMG) who currently have a confirmed diagnosis of PTSD (ICD-10: F43.1) or cPTSD (ICD-11: 6B41).

Exclusion criteria

Exclusion criteria: Lack of capacity to consent, treatment according to PsychKG during examinations, severe cognitive disorders, lack of German language skills.

Design outcomes

Primary

MeasureTime frame
Study no 1: 1. Presence of PTSD or cPTSD according to ICD-11, using ITQ (International Trauma Questionnaire, German version), 1 measurement time point. 2. Subjective level of suffering, using the scores of TIGER (Trauma Inventory Göttingen to record (k)PTSD) developed specifically for the study, 1 measurement time point. 3. Symptom frequency, using the scores ??of TIGER questionnaire (Trauma Inventory Göttingen to record (k)PTSD) developed specifically for the study, 1 measurement time point. 4. BPD symptomatology, using BPQ (Borderline Personality Questionnaire, German version), 1 measurement time point. 5. Psychiatric comorbidities (anxiety and depression), using the total score of PHQ-9 (Patient Health Questionnaire, German version) and GAD-7 (Generalized Anxiety Disorder Scale-7), 1 measurement time point. 6. Type of traumatic experiences, using the trauma categories in TEC (Traumatic Experiences Checklist, German version), 1 measurement time point. 7. Frequency of traumatic experiences, using the number of traumatic experiences recorded in TEC (Traumatic Experiences Checklist, German version), 1 measurement time point. 8. Age at the time of trauma, using the age recorded in TEC during the respective traumatic experience (Traumatic Experiences Checklist, German version), 1 measurement time point. Study no. 2 (Completed): 1. value stability of the TIGER (retest reliability)

Secondary

MeasureTime frame
Study no. 1: Sociodemographic differences in age, gender and level of education, using sociodemographic questions on age, gender and level of education, 1 measurement time point.

Countries

Germany

Contacts

Public ContactMarit Treptow

Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Göttingen (UMG)

marit.treptow@med.uni-goettingen.de0551-3962007

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026