F45.41
Conditions
Interventions
Group 1: Patients after the 4-weeks semi-residential multi-modal pain therapy: directly following the booster follow-up (2-3 months after the pain therapy), patients get SMS on 5 days a week over a pe
Sponsors
Universitätsklinikum Jena
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Intervention group: - meeting inclusion criteria for multi-modal pain therapy - informed consent - availability of a mobile phone - ability to read and write SMS - knowledge of German language. Comparison group: - meeting inclusion criteria for multi-modal pain therapy - informed consent
Exclusion criteria
Exclusion criteria: - not meeting one or more of the inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Feasibility test of a telemedical intervention and its acceptance by the patient population. Acceptance is assessed by use of a patient questionnaire that will be completed 2 months after end of the telemedical intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| 2. change of pain intensity (assessed by use of BPI) 3. change of pain-caused impairments (assessed by use of Korff-scale) 4. change of health-related quality of life (assessed by use of SF-12) Time of assessment: 4 weeks and 2 months after end of intervention | — |
Countries
Germany
Contacts
Public ContactKevean Mönchgesang
Universitätsklinikum JenaKlinik für Anästhesiologie und IntensivmedizinSection Schmerztherapie
Outcome results
None listed