Breast Cancer Clinical Trial
Improving Cancer Outcomes Through Personalized Care Planning and Symptom Management.
Summary
This Study is a case control Study conducted with 100 patients with a solid tumor cancer diagnosis (lung, breast, or gynecologic cancer). Records of 50 patients who received treatment plans as standard of care will be abstracted for control data. 50 patients undergoing cancer treatment will receive a treatment plan and report symptoms using Carevive PROmPTâ„¢.
Eligibility Criteria
Inclusion Criteria:
All participants must be 18 years of age or older.
Subject participants must have a diagnosis of a breast, lung, or gynecologic cancer.
Patients must have completed their navigation visit and received a Treatment Care Plan.
Subjects must be able to complete on-line surveys using a cell phone, tablet, or computer.
Subjects must be starting or receiving treatment.
All participants must be able to understand English.
Exclusion Criteria:
Any patient who cannot understand written or spoken English.
Any patient without the ability to complete on-line surveys using a cell phone, tablet, or computer.
Any prisoner and/or other vulnerable persons as defined by NIH (45 CFR 46, Subpart B, C and D).
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
Mobile Alabama, 36604, United States
How clear is this clinincal trial information?

Please confirm you are a US based health care provider:
Yes, I am a health care Provider No, I am not a health care providerSign Up Now.
Take Control of Your Disease Journey.
Sign up now for expert patient guides, personalized treatment options, and cutting-edge insights that can help you push for the best care plan.