Chronic Pain
Conditions
Interventions
Group 1: Patients in the outpatient specialized pain therapy
Based on existing data from clinical documentation, the project aims to determine the extent to which the severity of the disease and the c
Sponsors
Charité - Universitätsmedizin Berlin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with medical consultation in the specialized pain medicine of the Charité CCM and CVK
Exclusion criteria
Exclusion criteria: Incomplete data
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of relevant pain reduction (at least 30% pain reduction based on the Visual Analog Scale between onset and progression after 1 year). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Quantitative collection of psychometric scores from the German Pain Questionnaire (Pfingsten et al., 2015) from the treatment routine. - Qualitative survey on pain medication (e.g., use of opioids, coanalgesics, cannabinoids, phytotherapeutics) as well as survey on tolerability and discontinuation of medication - Documented quality of life of the patients - Frequency of physical and behavioral psychological co-treatment - Evaluation of the course of treatment by therapists and patients as documented in routine treatment. - Identification of patients with chronic postsurgical pain (CPSP) - Analysis of risk factors of chronic postsurgical pain and development of a risk model | — |
Countries
Germany
Contacts
Public ContactJan Wandrey
Charité - Universitätsmedizin Berlin
Outcome results
None listed