The goal of this clinical trial is to learn if psychoeducational intervention (tailored education, coping strategies, and guided disease disclosure) in a culturally appropriate format is beneficial in Reducing Anxiety, Depression, and Symptom Burden Among Omani Women Diagnosed with Breast Cancer. Patients receiving the intervention will be compared to Women who received standard medical care with no added psychoeducational content.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Anxiety and depression using the Hospital Anxiety and Depression Scale (HADS)
Timeframe: At baseline the time of the first chemotherapy session and at 9 months follow-up