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Clinical Trials in the USA / NCT05974150
Recruiting Observational

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

NCT05974150 · tracked via the Priya Life Science USA tracker
Sponsor
Carevive Systems, Inc.
Phase
Observational
Started
2023-07-19
Last updated
2026-02-23

Condition(s) studied

Breast CancerLung CancerMultiple MyelomaOvarian CancerAcute Myelogenous Leukemia

Investigational drug(s) / intervention(s)

Web based survey

Web based survey: online weekly survey

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
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).

Primary outcome measure(s)

Trial sites (7)

FacilityCityRegionStatus
Yale Cancer Center New Haven Connecticut Completed
Northshore University Health System Evanston Illinois Recruiting
Univeristy of North Carolina at Chapel Hill Chapel Hill North Carolina Completed
Duke Durham North Carolina Completed
Cleveland Clinic Mercy Hospital Canton Ohio Recruiting
University Hospitals Seidman Cancer Center Cleveland Ohio Recruiting
Tri-County Hematology & Oncology Associates, Inc. Massillon Ohio Recruiting

More Carevive Systems, Inc. trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05974150 on ClinicalTrials.gov ↗ ← All trials in the USA