C50 C81-C96 C51-C58
Conditions
Interventions
Group 1: Control group: The study participants receive the clinic program (usual care). The participants receive one and four months after discharge an interview via telephone, asked for their health
Sponsors
Verein zur Förderung der Rehabilitationsforschung e.V., Norderney
Eligibility
Sex/Gender
All
Age
No minimum to 62 Years
Inclusion criteria
Inclusion criteria: Oncological patients, see below Exclusion Criteria
Exclusion criteria
Exclusion criteria: (1) Advanced tumor / palliative situation, (2) insufficient German knowledge, (3) patient is retired (old-age pension / unlimited EU pension), (4) patient is older than 62 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measuring time 3 and 6 months after discharge The functional capability in occupational (measuring instrument IRES-3; Bührlen et al. 2005) | — |
Secondary
| Measure | Time frame |
|---|---|
| Measuring time 3 and 6 months after discharge Occupational stress and coping inventory (measuring instrument: AVEM; Schaarschmidt & Fischer, 2006) Subjective prognosis for gainful employment (measuring instrument: SPE-Scale; Mittag & Raspe, 2003) | — |
Countries
Germany
Contacts
Public ContactHeike Kähnert
Institut für Rehabilitationsforschung, Norderney: Abteilung Bad Salzuflen
Outcome results
None listed