Breast Cancer
Conditions
Interventions
Intervention group:CRCI intervention scheme constructed in this study.
Control group:Routine nursing
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Pathological diagnosis of breast cancer; 2. Initial treatment, chemotherapy planned; 3. Age >= 18 years; 4. Informed consent, patient voluntarily participates in this study.
Exclusion criteria
Exclusion criteria: 1. Presence of concurrent malignancies; 2. Patients with brain metastases, or severe systemic diseases affecting major organs (e.g., heart, brain, lungs, kidneys); 3. History of psychiatric disorders, or impaired verbal/written communication abilities.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional Assessment of Cancer Therapy-Cognitive Function Score ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pittsburgh Sleep Quality Index, PSQI;Hospital Anxiety and Depression Scale Score;Functional Assessment of Chronic Illness Therapy-Fatigue Score;Quality of Life Assessment Form for Breast Cancer Patients Score; | — |
Countries
China
Contacts
Public ContactMou Qianqian
West China Hospital, Sichuan University
Outcome results
None listed