C56 C50
Conditions
Interventions
Group 1: Patients with breast or ovarian cancer who are indicated for chemotherapy due to their tumor biology will be offered to participate in the study. After approval, the interview takes place. He
Sponsors
Kliniken Essen Mitte
Eligibility
Sex/Gender
Female
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Age >18 years Initial chemotherapy treatment at the Department of Gynecology & Gynecologic Oncology of the Essen-Mitte Hospital for senological or gynecological tumors Willingness to participate in the study + signed consent form
Exclusion criteria
Exclusion criteria: Lack of German understanding Reading difficulties / illiteracy expected life duration of therapy <3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| This prospective study aims to investigate how side effects of systemic therapy of patients with gynecologic malignancies are perceived and assessed / categorized in their significance. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of perception of side effects and their importance in patients undergoing maintenance therapy • Evaluation of perception of side effects at different times of treatment | — |
Countries
Germany
Contacts
Public ContactBeyhan Ataseven
Kliniken Essen Mitte
Outcome results
None listed