Malignant Glioma Clinical Trial
Official title:
Comparative Development of Data Driven Systems for Insuring Timely Monitoring for Brain Tumor Patients for Management of Myelosuppression
This research trial studies an adherence monitoring system in managing myelosuppression in patients with newly diagnosed malignant gliomas who are receiving temozolomide and radiation therapy. The development of an adherence monitoring system may help doctors more effectively utilize electronic medical records to manage myelosuppression during standard treatment with temozolomide and radiation therapy in patients with malignant gliomas.
PRIMARY OBJECTIVES:
I. To develop an adherence monitoring system within Epic that is functionally equivalent to
the previously designed and validated system in the Cancer Center Oncology Research
Information System (ORIS) for patients with newly diagnosed malignant gliomas receiving
concurrent temozolomide and radiation therapy.
II. To test the newly designed Epic system by comparing the frequency and timing of flags
(laboratory date flags, visit date flags and in-patient status flags) and non-adherent days
generated with the frequency and timing of those generated by ORIS for patients with newly
diagnosed malignant gliomas receiving concurrent temozolomide and radiation therapy.
SECONDARY OBJECTIVES:
I. To develop both systems so that they may be easily adapted in the future to other
therapies that require compliance monitoring.
OUTLINE:
Patient lab and visit dates are monitored by the Cancer Center ORIS and EPIC based systems
during the 42 days of the concurrent temozolomide and radiation therapy.
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