Pain chronicity and impairment, quality of life, depression, anxiety and PTSD. N80
Conditions
Interventions
Group 1: Patients with endometriosis are interviewed about the following areas:
- anamnesis questionnaire
- Chronic pain (Gerbershagen)
- Pain Disability Index (PDI)
- Depression & Anxiety (HADS)
- Qu
Sponsors
Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie des Universitätsklinikum des Saarlandes
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Included in the experimental group are only female patients >18 years, with the secured diagnosis endometriosis (by a gynecological specialist), who give their written consent to participate in the study.
Exclusion criteria
Exclusion criteria: Excluded are all patients <18 years, as well as those who refuse to participate in the study. Also excluded are subjects with cognitive limitations that make a questioning impossible, subjects with whom the communication seems impossible for example because of deafness, illiteracy, not being able to communicate in german, unresponsive deafness etc. Furthermore, all subjects with previous gynecological diseases (except endometriosis) are excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| One-time questionnaire investigation on stages of chronicity, pain, quality of life and psychological factors in patients with endometriosis. The questionnaire consists of the following parts: Disease anamese, pain chronicity (according to Gerbershagen), Pain Disability Index (PDI), Hospital Anxiety and Depression Scale (HADS), Short Form 12 (SF12), Childhood Trauma Screener (CTS), ICD11 Trauma Questionnaire and Questionnaire for partnership diagnostics, FPD. | — |
Countries
Germany
Contacts
Public ContactSvenja Kreutzer
Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie des Universitätsklinikum des Saarlandes
Outcome results
None listed