The data registry collects longitudinal data reflecting patient history, pain, psycho-social factors, quality of life, physical exam pain mapping, specialized ultrasound results, surgical findings and pathology. This includes the completion of validated questionnaires yearly for up to 5 years to assess depression (PHQ-9), generalized anxiety (GAD-7), pain catastrophizing (PCS), sleep scale, and endometriosis health profile (EHP-30).
With a goal of better understanding endometriosis we are particularly interested in:
- Predictors of chronic pelvic pain
- Sexual pain
- Sexual quality of life
- Central sensitization
- Characterizing endometriosis
- Linking gene mutations to clinical symptoms
- Exploring transnational and behavioural implications of our research findings
Further information about our publications can be found at https://yonglab.med.ubc.ca/.