Oncology
Conditions
Brief summary
This is an investigational multi-site outcomes registry intended to collect information about a patient's cancer care. Patients may enter the Registry at any time during the patient's current stage in the continuum of care. The registries main objectives will be to measure and evaluate the effects of patient care throughout the care continuum, resulting in the identification of the most effective treatment options. Objectives will encompass evaluations and analytics around safety, effectiveness, and improved efficiencies.
Detailed description
Q
Interventions
OTHERPatient registry
Oncology data registry
Sponsors
SCRI Development Innovations, LLC
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 18 or older * Patients that have been diagnosed with/ or are thought to have any form of cancer at any stage in the continuum of their care from screening through survivorship. * Patient must have the ability to understand the nature of the trial and give written informed consent
Exclusion criteria
* There are no
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| quality improvement | 10 yrs |
| Treatment patterns and utilization | 5 yrs |
Secondary
| Measure | Time frame |
|---|---|
| Humanistic and economic outcomes | 10 yrs |
Other
| Measure | Time frame |
|---|---|
| safety and effectiveness | 10 yrs |
Countries
United States
Outcome results
None listed