R52
Conditions
Interventions
Group 1: The participants in this study will be asked to document their current pain and impairment of wellbeing twice daily (before and after therapy sessions), using both the eEgg and the NRS method
Sponsors
Zentrum für Interdisziplinäre Schmerztherapie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Informed consent must be signed - Patients must be registered with the Centre for Interdisciplinary Pain Medicine (Zentrum für interdisziplinäre Schmerzmedizin)
Exclusion criteria
Exclusion criteria: - insufficient understanding of the German language - disorders of the motoric system concerning the upper extremity - acute/urgent required treatment of neurological or psychiatric illnesses - allergies to the eEgg-material - different circumstances, that argue against participation in this trial from a medical perspective
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Data concerning patients’ pain intensity (acquired using the NRS and eEgg method) is tested for relationship. | — |
Secondary
| Measure | Time frame |
|---|---|
| Data concerning patients’ impairment of wellbeing (acquired using the NRS and eEgg method) is tested for relationship. | — |
Countries
Germany
Contacts
Public ContactJanosch A. Priebe
Zentrum für Interdisziplinäre Schmerztherapie
Outcome results
None listed