Mobile, Alabama 36604

  • Gynecologic Cancer

Purpose:

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 PROmPT™.


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).


NCT ID:

NCT04772118


Primary Contact:

Julie Scott, RN,MSN
Phone: 18004603790
Email: julie.scott@carevive.com


Backup Contact:

Email: Debbie@carevive.com
Debra Wujick, RN, PhD
Phone: 18004603790


Location Contact:

Mobile, Alabama 36604
United States

Jenna James, MPH
Phone: 251-445-9667
Email: jmjames@health.southalabama.edu

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 20, 2021

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