C50
Conditions
Interventions
Group 1: 30 women participating in breast cancer rehabilitation are interviewed using a newly developed screening tool at the start of their rehabilitation programme. In addition, the participants are
Sponsors
Universität zu Lübeck, Institut für Sozialmedizin und Epidemiologie
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: The study includes women aged 18 to 65 who are participating in a breast cancer rehabilitation programme at the Asklepios Nordseeklinik Westerland.
Exclusion criteria
Exclusion criteria: Rehabilitation patients without a confirmed diagnosis of breast cancer and who have insufficient knowledge of German will be excluded from the study. In addition, not consenting to take part in the study is an exclusion criterion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The screening tool to be developed and tested as part of the study consists of various predictors, such as socio-demographic characteristics, disease-related variables, comorbidities, patient-reported outcome measurements and individual items. The comprehensibility and feasibility of the tool will be assessed among patients undergoing breast cancer rehabilitation through cognitive interviews and a written questionnaire at the start of their rehabilitation. In guideline-based interviews, rehabilitation staff will be surveyed about the tool’s acceptability, comprehensibility, time requirements and the feasibility of integrating the tool into existing processes. | — |
Secondary
| Measure | Time frame |
|---|---|
| Socio-demographic characteristics, subjective health status and comorbidities of the rehabilitation participants are assessed at the start of rehabilitation using a written questionnaire. | — |
Countries
Germany
Contacts
Public ContactMercedes Rutsch
Universität zu Lübeck
Outcome results
None listed