Effectiveness of an autonomous rehabilitation algorithm in cancer patients
Not Applicable
Recruiting
- Conditions
- D48Neoplasm of uncertain or unknown behaviour of other and unspecified sites
- Registration Number
- DRKS00015818
- Lead Sponsor
- RWTH Uniklinik Aachen Abteilung für Mund-, Kiefer- und Gesichtschirurgie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 400
Inclusion Criteria
All patients who are undergoing in-patient treatment for cancer can be included.
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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The study investigates the efficacy of an autonomous rehabilitation plan for length of hospitalization and postoperative complications.<br><br>What? Comparison of length of stay and postoperative complications between both groups<br>When? Patients of the control group and the intervention group are interviewed at the end of the inpatient stay and after about 1 month<br>How? self-developed questionnaires
- Secondary Outcome Measures
Name Time Method The study investigates the influence of an autonomous rehabilitation plan on patients' subjective feelings about their physical and mental well-being.<br><br>What? Comparison of physical and mental well-being between intervention and control group<br>When? Patients of the control group and the intervention group are interviewed at the end of the inpatient stay and after about 1 month<br>How? self-developed questionnaires