Purpose

The goal of this study is to create a data set to add to Carevive's registry from real world clinical and patient reported data collected using an electronic care planning system (CPS) with remote symptom monitoring that is used in routine care for cancer patients on active treatment. Patients will complete a baseline survey in person using a secured device or remotely using their own electronic device in a location of their choice. Weekly electronic patient reported outcome (PRO) surveys are collected from the patients using the Carevive platform for a minimum of 12 weeks. Patients may continue weekly surveys as long as they are receiving treatment.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All participants must be 18 years of age or older. - Subjects may be any stage and anywhere in the treatment continuum. - Subject participants must have a diagnosis of a breast, lung, AML, ovarian cancer or multiple myeloma. - Subjects must be able to complete on-line surveys using a cell phone, tablet, or computer. - 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 patient on a treatment clinical trial. - Any prisoner and/or other vulnerable persons as defined by NIH (45 CFR 46, Subpart B, C and D).

Study Design

Phase
Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Recruiting Locations

Northshore University Health System
Evanston, Illinois 31024
Contact:
Michele Britto
MBritto@northshore.org

Cleveland Clinic Mercy Hospital
Canton, Ohio 44708
Contact:
Janet Muckley
MUCKLEJ@ccf.org

University Hospitals Seidman Cancer Center
Cleveland, Ohio 44106
Contact:
Jill Severino-Powell, MSN
Jill.Severino-Powell@UHhospitals.org

Tri-County Hematology & Oncology Associates, Inc.
Massillon, Ohio 44646
Contact:
Janet Muckley
MUCKLEJ@ccf.org

More Details

NCT ID
NCT05974150
Status
Recruiting
Sponsor
Carevive Systems, Inc.

Study Contact

JULIE SCOTT, MSN
8778423210
Julie.Scott@Carevive.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.