Improving Cancer Outcomes Through Personalized Care Planning and Symptom Management.

Carevive Systems

Status

Completed

Conditions

Breast Cancer

Gynecologic Cancer

Lung Cancer

Treatments

Other: Carevive PROmpt™

Study type

Interventional

Funder types

Industry

Identifiers

NCT04772118

G423 Multi TP

Details and patient eligibility

About

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™.

Enrollment

51 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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).