Cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Females aged 18–65 years Confirmed breast cancer (histopathology/cytology) Written informed consent Willing to adhere to intervention protocol
Exclusion criteria
Exclusion criteria: Cognitive/psychiatric conditions affecting adherence Concurrent clinical trial participation Pregnancy/breastfeeding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body composition parameter (Body weight, BMI, fat mass, lean muscle mass, waist-to-hip ratio) change from baseline to end line in g months of intervention in breast cancer patients receiving multimodal interventions. | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in Biochemical profiles (Lipid profiles, CBC, glucose level, Liver/Kidney function Tests);Change in Nutritional status (PG-SAG, food diversity score, haemoglobin level, etc.) ;Change in Clinical Outcomes after multimodal intervention | — |
Countries
Ethiopia
Contacts
Lecturer and assistant professor at Jimma University