CHRONISCHESCHMERZEN
Conditions
Interventions
Group 1: The participants in the group "observational vid" will learn in the video that the placebo effect works even if they know that it is a placebo. They see a video with a chronic pain patient wh
Sponsors
UKE Universitätsklinikum Hamburg Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: All participants have to be at least 18 years old, have no strong cognitive impairment and sufficient German reading and speaking abilities (writing and reading). At the beginning of the study the patients must have chronic pain. In order to be included in this voluntary study the patients have to fulfill these criteria and give their written consent.
Exclusion criteria
Exclusion criteria: Excluded will be patients who do not or can not declare their consent (e.g. incomliance or dementia) and/or are not sufficiently able to read, write or speak german and their overall health status does not allow a participation in the study because of health reasons. Excluded are also patients with primary headaches or facial pain.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the change in in expectation and the willingness to take OLP via observational learning on a 4 point scale. This will be asked after watching the video. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome is the influence of the predictors depression, empathy and personality traits on the change in the willingeness to take OLP. | — |
Countries
Germany
Contacts
Public ContactRegine Klinger
Dep. of Anaesthesiology, Universitätsklinikum Hamburg-Eppendorf (UKE)
Outcome results
None listed