Improving Cancer Outcomes Through Personalized Care Planning and Symptom Management.

Completed · Not applicable

Conditions studied: Lung Cancer, Breast Cancer, Gynecologic Cancer

In brief

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™.

Key facts

Study ID

NCT04772118

Run by

Carevive Systems, Inc.

People needed

51

Starts

2021-02-16

Expected to finish

2021-11-01

Last updated by the study team

2022-01-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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).

Where it is running

• Mitchell Cancer Institute — Mobile, Alabama, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.