M00-M99
Conditions
Interventions
Group 1: Control group: The study participants receive the conventional medical rehabilitation (usual care).
Group 2: Intervention group: The study participants are treated after the implementation of
Sponsors
Verein zur Förderung der Rehabilitationsforschung e. V., Norderney
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Orthopaedic Patients of the medical centers "Salzetalklinik" and "Klinik am Lietholz" (both in Bad Salzuflen, Germany), specific work-related problems (screening instrument: SIMBO-C), informed consent
Exclusion criteria
Exclusion criteria: acute disease and follow-up rehabilitation, cognitive impairments, insufficient German knowledge, insufficient physical cabability or motivation, patient is retired (old-age pension or unlimited EU pension)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The functional capability in occupation (measuring instrument: IRES-3; Bührlen et al. 2005) Measuring time: 3 and 6 months after discharge | — |
Secondary
| Measure | Time frame |
|---|---|
| Health state (measuring instrument: EQ-5D); subjective prognosis for gainful employment (measuring instrument: SPE-scale); work ability (measuring instrument: work ability index) Measuring time: 3 and 6 months after discharge | — |
Countries
Germany
Contacts
Public ContactPhilipp Preßmann
Institut für Rehabilitationsforschung Norderney, Abteilung Bad Salzuflen
Outcome results
None listed