Breast cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Female patients with incipient breast cance 2) The first use of our outpatient chemotherapy room during this study
Exclusion criteria
Exclusion criteria: 1) Incapable of consent to this study 2) History of chemotherapy during admission 3) History of other malignant tumors 4) History of radiotherapy 5) Existence of brain metastasis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcomes are objective cognitive function scores in verbal fluency tasks, a part of Wechsler Memory Scale-Revised (WMS-R), Trail Making Test A/B (TMT-A/B), a part of Wechsler Adult Intelligence Scale-III (WAIS-III). We will perform them before chemotherapy (T1), within a week after the end of 1st kind chemotherapy (T2), within a week after the end of 2nd kind chemotherapy (T3), and more than 3 months after the end of 2nd kind chemotherapy (T4). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcomes are subjective cognitive function scores in Everyday Memory Checklist, QOL scores in Functional Assessment of Cancer Therapy-Breast (FACT-B), psychiatric symptoms scores in Hospital Anxiety and Depression Scale (HADS). We will perform them before chemotherapy (T1), within a week after the end of 1st kind chemotherapy (T2), within a week after the end of 2nd kind chemotherapy (T3), and more than 3 months after the end of 2nd kind chemotherapy (T4). | — |
Countries
Japan
Contacts
Tokushima University Hospital Psychiatry