chronic/recurrent pelvic pain, dysmenorrhea, endometriosis N94.4 N94.5 N80 R10.2 N94.6
Conditions
Interventions
Group 1: Patients who participated in the initial project due to their endometriosis / chronic abdominal pain.
If they were in a relationship at the time of the initial project and their partner part
Sponsors
Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: participation in first project informed consent
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main goal of this study is to better understand how endometriosis and chronic pelvlic pain develop across 12 months. This will be assessed considering the impact of stress, social influences, and applied therapies. | — |
Secondary
| Measure | Time frame |
|---|---|
| Demographic data will be analyzed as covariates. | — |
Countries
Germany
Contacts
Public ContactKatharina van Stein
Institut für Medizinische Psychologie
Outcome results
None listed