M54
Conditions
Interventions
Group 1: Intervention group: Positive information about the medication (Amitriptilyn, individual dosage)-- Patients will be randomized and allocated to the intervention group. A social observational S
Sponsors
Universitätsklinikum Hamburg-Eppendorf (UKE)?Zentrum für Anästhesiologie und Intensivmedizin?Klinik und Poliklinik für Anästhesiologie?Bereich Schmerzmedizin und Schmerzpsychologie?
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with chronic back pain, ongoing treatment in the pain center of the UKE, ongoing medication: Amitriptyline.
Exclusion criteria
Exclusion criteria: Exclusion criteria: acute or chronic mentally disorders excluding: F45.41 (nach ICD-10; DSM-IV bzw. DSM-V), insufficient knowledge of German language or eye-sight, cognitive impairment or intake of medication, which impairs consciousness.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain rating: Numerical Rating Scale (NRS) 0-10, Pre-, Post-, 2 weeks follow up | — |
Secondary
| Measure | Time frame |
|---|---|
| pain associated variables: Pain Disability, functional capacity, depressive mood, pain catastrophizing, quality of life Pre, post, 2 weeks follow up (concerning experimental social learning situation) | — |
Countries
Germany
Contacts
Public ContactRegine Klinger
Universitätsklinikum Hamburg-Eppendorf (UKE)?Zentrum für Anästhesiologie und Intensivmedizin?Klinik und Poliklinik für AnästhesiologieBereichs Schmerzmedizin und Schmerzpsychologie?
Outcome results
None listed