Actively Recruiting
Total Cancer Care Protocol: A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer (ORIEN)
Led by University of Colorado, Denver · Updated on 2025-11-10
20000
Participants Needed
6
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying patients who have cancer or may be at risk of developing cancer to improve the standard of care. This observational study collects blood, tissue, and other biological samples along with associated data such as surveys, medical records, and cancer registry information. The goal is to enable new clinical trials, technology advancements, and personalized medicine for cancer patients over time. Participants provide consent to allow collection and storage of their biological samples and data. This includes blood and tissue samples as well as survey assessments and medical chart reviews. The study does not involve treatment but focuses on gathering information to support cancer research and care improvements. During the study, patients' biological samples and data are collected and stored long-term. Researchers analyze survey responses, medical records, and biological specimens to measure outcomes related to improving cancer care standards. The study follows participants for up to 20 years, aiming for a lifetime partnership to support ongoing cancer research and care advancements.
CONDITIONS
Brief Title
A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age and older
- Diagnosed with cancer or may be at risk for cancer
- Able to understand and sign the informed consent and research authorization form directly or through a legally authorized representative
- Non-English speaking individuals may participate using a short-form consent process
You will not qualify if you...
- Members of vulnerable populations including neonates (birth to 30 days), children under 18 years
- Wards of the State
- Prisoners or those on probation or alternate sentencing
- Adults or children who are cognitively impaired, incompetent to consent, or require proxy consent in life-threatening situations
- Decisionally challenged individuals unable to provide consent themselves
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 20 years
Participants provide blood, tissue, and other biological samples and complete surveys. Medical data is also collected from their health records over time to support cancer research.
Periodic visits as needed for sample collection and assessments
Trial Site Locations
Total: 6 locations
1
University of Colorado Hospital
Aurora, Colorado, United States, 80045
Actively Recruiting
2
UCHealth Memorial Hospital Central
Colorado Springs, Colorado, United States, 80909
Actively Recruiting
3
UCHealth Memorial Hospital North
Colorado Springs, Colorado, United States, 80909
Actively Recruiting
4
Cherry Creek Medical Center
Denver, Colorado, United States, 80206
Actively Recruiting
5
UCHealth Poudre Valley Health System
Fort Collins, Colorado, United States, 80528
Actively Recruiting
6
Highlands Ranch Medical Center
Highlands Ranch, Colorado, United States, 80126
Actively Recruiting
Research Team
K
Kyra Anderson
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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