The purpose of this study is to examine the effectiveness of a technology-based intervention for managing nausea and vomiting in older adults with cancer. Participants will be randomized to either an intervention or control group. Outcomes such as symptom severity, quality of life, and resource use will be examined.
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Healthcare resource use
Timeframe: From baseline through the end of the study at 12 or 24 weeks
CINV severity
Timeframe: From baseline1 through the end of the study at 12 or 24 weeks