This is a two part observational study evaluating the feasibility of implementing an
EHR-based model within a community oncology practice.
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT03028584
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Clinicians: Provide cancer care to BrCa, CRCa or PrCa
Clinicians: Are a physician, advanced practice practitioner, nurse, or equivalent
Patients: Have a diagnosis of breast, colorectal, or prostate cancer for which and EHR-based SCP will be provided
Patients: Have been treated with curative intent (e.g. surgery, chemotherapy and/or radiation therapy) for a Stage 1-3 cancer diagnosis
Patients: Have received some part of active cancer treatment
Patients: Have complete active treatment (defined as surgery, chemotherapy, and/or radiation therapy). HER2-based and endocrine therapies may be ongoing and do NOT need to have been completed
Unable to complete or unwilling to answer questions in English
Patients: Received all active cancer treatment elsewhere (e.g. "observation - only" patients)
Patients: Have metastatic cancer
All locations for NCT03028584
United States (1)
UW Cancer Center at ProHealth Care
Waukesha, Wisconsin, United States, 53188
View full eligibility
Tris trial is registered with FDA with number: NCT03028584. The sponsor of the trial is University of Wisconsin, Madison and it is looking for 30 volunteers for the current phase.
Official trial title: Feasibility of Delivering Electronic Health Record (EHR)-Based Survivorship Care Plans and Planning to Cancer Survivors in a Community Oncology Practice
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