Can Protein Intake be Increased Using Whole Foods Post-treatment in Cancer Patients?
Cancer, Other Malnutrition
About this trial
This is an interventional supportive care trial for Cancer focused on measuring Cancer, Nutrition, Protein, post-chemotherapy, Recovery, food-related quality of life
Eligibility Criteria
Inclusion Criteria: Patients must have the ability to read, understand, and sign an informed consent and must be willing to comply with study treatment and follow-up. ≥18 years of age Histopathologically confirmed cancer with receipt of a platinum chemotherapy during treatment; active treatment has concluded. Capable of volitional oral semi-solid intake at baseline; able to maintain oral intake over the trial. Exclusion Criteria: Fed by nasogastric tube, gastrostomy, or total parenteral nutrition Cancer of the brain, Cancer of the regions which impact an individual's ability to consume food. A known hypersensitivity / allergy to eggs. Enrolment in any other clinical protocol or investigational study that may interfere with study procedures. Poorly controlled chronic illnesses or other inflammatory diseases (e.g. Chronic Obstructive Pulmonary Disease(COPD), uncontrolled non-insulin dependent diabetes, rheumatoid arthritis). In a clinician opinion, patients who have medical conditions that could interfere with nutrient metabolism or absorption (e.g., short bowel syndrome, Crohn's disease, etc.)
Sites / Locations
- University of AlbertaRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Early Intervention
Delayed Intervention
Participants are expected to begin intervention immediately after the completion of treatment for a period of 8 weeks.
Participants are expected to begin intervention 4 weeks after the completion of the treatment, for a period of 4 weeks (weeks 5-8).