D48
Conditions
Interventions
Group 1: Intervention Group (standard clinical physiotherapy + autonomous Rehabilitation plan)
Group 2: control group 1 (standard clinical physiotherapy)
Group 3: control group 2 (no physiotherapy, bu
Sponsors
RWTH Uniklinik Aachen Abteilung für Mund-, Kiefer- und Gesichtschirurgie
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: All patients who are undergoing in-patient treatment for cancer can be included.
Exclusion criteria
Exclusion criteria: Exclusion criteria are a rejection of study participation. Patients under 18 years, pregnant women and non-consenting patients are also excluded from participating in the study. Furthermore, a significantly reduced physical or emotional general condition is an exclusion criterion. Should the patients wish to stop the study at any time, this will be dealt with immediately.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study investigates the efficacy of an autonomous rehabilitation plan for length of hospitalization and postoperative complications. What? Comparison of length of stay and postoperative complications between both groups When? Patients of the control group and the intervention group are interviewed at the end of the inpatient stay and after about 1 month How? self-developed questionnaires | — |
Secondary
| Measure | Time frame |
|---|---|
| The study investigates the influence of an autonomous rehabilitation plan on patients' subjective feelings about their physical and mental well-being. What? Comparison of physical and mental well-being between intervention and control group When? Patients of the control group and the intervention group are interviewed at the end of the inpatient stay and after about 1 month How? self-developed questionnaires | — |
Countries
Germany
Contacts
Public ContactJulius Steegmann
RWTH Uniklinik Aachen Abteilung für Mund-, Kiefer- und Gesichtschirurgie
Outcome results
None listed