Protein Needs Study

What this study is about

Severe muscle loss in patients with cancer has been associated with increased physical disability, extended hospitalization, infectious and noninfectious complications, increased risk of severe toxicity during cancer treatment, poor quality of life and shortened survival. Adequate protein is key to sustain muscle mass and overall health. However, current nutritional recommendations are not specific or evidence-based. The aim of this project is to determine the protein needs of patients with colorectal or breast cancer. Protein needs will be determined using a novel, non-invasive approach. Our results will inform nutritional recommendations and guidelines with the ultimate goal of improving outcomes for people with cancer.

Who can join (things the study team will check)

✅ You may be able to join if…

• Outpatients age 45-80 years;
• Patients attending the new patient clinic at the Cross Cancer Institute with a diagnosis of colorectal cancer or breast cancer (stages II to III);
• Able to complete baseline visits within approximately 4 weeks of starting chemotherapy OR after a minimum of 4 weeks post-surgery if not undergoing chemotherapy;
• Ambulatory.

🚫 You may not be able to join if…

• Premenopausal women due to impact on protein requirements;
• Received anti-cancer hormone treatment or immunotherapy in the 4 weeks before first baseline visit;
• Renal impairment based on a creatinine clearance for estimated glomerular filtration rate (eGFR) of <60 mL/min
• Abnormal glucose metabolism based on a fasting glucose level >6mmol/L and an HbA1c >5.7% or as reviewed by study team;
• Comorbidities or medications that would interfere with the participants ability to follow the study protocol or the quality of the data(e.g. diabetes, class III obesity, hormone therapy, another active cancer diagnosis);
• Unable/unwilling to provide urine, breath and blood samples (e.g. oxygen tank, catheter, etc.);
• Unable to eat the meals provided (i.e. receiving parenteral or enteral nutrition, severe allergies);
• Substance dependent (e.g. alcohol, cigarettes, illicit drugs) and unable to follow study protocols.

Where this trial is running

• University of Alberta, Edmonton, Alberta, Canada

Who to contact

Anne Caretero, RD · 780-492-7820 · caretero@ualberta.ca

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT04144907.