Software Monitoring of Treatment Related Toxicities in Advanced Renal Cell Carcinoma



Status:Not yet recruiting
Conditions:Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:2/23/2019
Start Date:April 2019
End Date:July 2022

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Monitoring of Treatment Related Toxicities From Oral Targeted Agents and Immunotherapy Among Patients With Advanced Renal Cell Carcinoma (RCC) Using Carevive Software, a Single-Arm Phase II Feasibility Study

To determine if Carevive software, which monitors treatment-related toxicities and then
generates self-care management plans for these symptoms, will be feasible to implement among
patients with metastatic renal cell carcinoma (RCC). Additionally for collection of
preliminary data on treatment-related toxicities, quality of life, distress level, and drug
adherence.


Inclusion Criteria:

- Diagnosis of histologically confirmed renal cell carcinoma of any subtype with either
pathological or radiographic evidence of metastatic disease

- Greater than 18 years of age

- A participating Wilmot Cancer Center oncologist has determined that candidate should
be started on either oral targeted therapy or immunotherapy for treatment of their
advanced RCC; this can be for first-line or any subsequent line therapy

- Able to provide written informed consent

- Proficient in the English language and self-reports as literate

- Must have an active email address or access to a smart device on which text messages
can be received

Exclusion Criteria:

- Women cannot be breast-feeding

- Does not have regular access to the internet

- Unable to come to the Wilmot Cancer Center for appointments every 3-4 months for
routine visits with their primary oncologist

- Subjects who were on the study previously will not be allowed to re-enroll in the
event of a treatment change
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