Optimisation of the digital health platform/software already established at the University Hospital Halle (Saale) for recording patient-reported quality of life and symptoms in the presence of cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Patients of the University Clinic and Polyclinic for Gynaecology of the University Hospital Halle (Saale) who are treated in the gynaecological day clinic or outpatients, who are treated in the radiological outpatient clinic - Diagnosed underlying oncological disease [in the field of gynaecology (malignant tumours of the fallopian tubes, ovaries, uterus and cervix) or for radiotherapy all tumours - Existing legal capacity - No cognitive impairments (e.g. in the sense of a neurological disease or dementia) - Sufficient knowledge of written and spoken German - Available and signed declaration of consent
Exclusion criteria
Exclusion criteria: - External patients from other hospitals - Lack of treatment in the gynaecological day clinic at the UKH - Patients without a gynaecological-oncological clinical picture - Patients with breast cancer, as they are already being cared for elsewhere in programmes and studies - Patients with cognitive impairments (e.g. in the sense of a neurological disease or dementia) - Patients who have refused or withdrawn their consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The objective is to adapt the existing digital health platform/software in a user-centred manner so that it can be implemented (as a model) in other clinical areas of the university hospital. The digital assistance system, which is designed to support oncology pilots, aims to enhance the quality of treatment for oncological patients in the Halle (Saale) region while simultaneously alleviating the burden on those treating them at the University Hospital Halle (Saale). | — |
Secondary
| Measure | Time frame |
|---|---|
| - The objective is to ascertain the needs, requirements and demands, as well as expectations, of users (in particular patients) of the digital health platform. To this end, the standardised EORTC questionnaires (PATSAT-C33, OUT-PATSAT7, QLQ-INFO25) and the SUS questionnaire are collected at two measurement points (t0, t1). Furthermore, a practical evaluation of the digital health platform was conducted at measurement time point t1, utilising the think-aloud method and a guided individual interview. - Target 2: Determine the change in usability using the SUS questionnaire. - Target 3: Determine the change in user acceptance using the SUS questionnaire. | — |
Countries
Germany
Contacts
AG Versorgungsforschung - Pflege im Krankenhaus