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PRO-VISION: Patient Reported Outcomes-Based Monitoring of VEGF-Inhibitor Side Effects in ONcology
Sponsor: UNC Lineberger Comprehensive Cancer Center
Summary
The purpose of this study is to investigate how collecting information about treatment-related side effects directly from patients can help manage the side effects associated with certain oral chemotherapies. This study is specifically investigating this approach in patients taking oral vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitors (TKIs) for metastatic renal cell carcinoma (mRCC). Participants in this study will receive a survey via email or telephone once a week while receiving treatment with a VEGFR TKI. The survey will ask about symptoms such as nausea or fatigue and overall quality of life. This survey should take no more than 15 minutes to complete. The survey will be sent directly to the oncology care team. Participants will receive a follow-up phone call or message from the team when participants have new or worsening symptoms. The participants will continue to receive surveys for as long as they are receiving a VEGF TKI treatment.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
42
Start Date
2022-03-18
Completion Date
2031-01-16
Last Updated
2025-05-13
Healthy Volunteers
No
Conditions
Interventions
Survey Questionnaire
Study participants will complete several questionnaires/assessments via PRO-Core standardized email communication or via telephone with a study team member.
Locations (1)
Lineberger Comprehensive Cancer Center
Chapel Hill, North Carolina, United States