About this trial
This trial tests an online nutrition education program focused on decreasing nutrition-related side effects of chemotherapy in patients with breast cancer. Patients undergoing chemotherapy are at risk for complications such as diarrhea or constipation which can lead to poor nutritional intake and malabsorption of nutrients. This study is testing the effects of information delivered via the Cook for Your Life website in conjunction with standard clinical care to improve symptom management during chemotherapy treatment for breast cancer, which could serve as a new model for supportive oncology care.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
18 years of age or older.
Stage I-III breast cancer.
Current breast cancer patients scheduled to receive ddAC-T(+/-C), TCHP, or TCPembro-AC chemotherapy at Fred Hutch South Lake Union (can enroll prior to receipt of 2nd cycle).
Not pregnant and no plan to become pregnant during chemotherapy treatment.
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Best Practice
Other interventionReceive standard of care
Internet-Based Intervention
BehavioralAccess to enhanced Cook for your life website
Questionnaire Administration
Other interventionAncillary studies
Treatment groups
Trial outcomes
Primary outcomes
Accrual rate
Accrual rate to the study.
Use of cook for your life website pages (adherence: visiting website) will be measured via Google analytics
Google analytics will be used to identify whether participants visit the website.
Use of cook for your life website pages (adherence: webpages viewed) will be measured via Google analytics
Google analytics will be used to identify what webpages participants view.
Time of use of cook for your life website (adherence: total time) will be measured via Google analytics
Google analytics will be used to measure how much total time spent on the website.
Secondary outcomes
Incidence of patient-reported nutrition-related adverse events
Patient-reported nutrition-related adverse events assessed via the chemotherapy patient reported outcome (PRO) tool.
Number of participants with treatment delays and causes of delays
Treatment delays and causes of delays as assessed via chart abstraction
Delivered dose of planned treatment
Assessed via chart abstraction.
Change in dose
Assessed via chart abstraction.
Sponsors and contacts
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