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RECRUITING
NCT05974150

Real World Treatment Experience of Patients With Breast, Lung, Ovarian, Multiple Myeloma, or Acute Myelogenous Leukemia Using Remote Symptom Monitoring

Sponsor: Carevive Systems, Inc.

View on ClinicalTrials.gov

Summary

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.

Official title: Real World Treatment Experience of Patients With Breast, Lung, Ovarian, Multiple Myeloma, or Acute Myelogenous Leukemia (AML) Using Remote Symptom Monitoring

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

25

Start Date

2023-07-19

Completion Date

2026-12-31

Last Updated

2026-02-23

Healthy Volunteers

No

Interventions

OTHER

Web based survey

online weekly survey

Locations (7)

Yale Cancer Center

New Haven, Connecticut, United States

Northshore University Health System

Evanston, Illinois, United States

Univeristy of North Carolina at Chapel Hill

Chapel Hill, North Carolina, United States

Duke

Durham, North Carolina, United States

Cleveland Clinic Mercy Hospital

Canton, Ohio, United States

University Hospitals Seidman Cancer Center

Cleveland, Ohio, United States

Tri-County Hematology & Oncology Associates, Inc.

Massillon, Ohio, United States