Actively Recruiting
Norris ORIEN Total Cancer Care Protocol: A Lifetime Partnership With Patients
Led by University of Southern California · Updated on 2026-04-29
10000
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
U
University of Southern California
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are collecting biological samples and clinical information from patients who have cancer or are at risk for cancer to create a large repository. This study aims to combine genetic data from these samples with clinical information to better understand why some cancers respond to treatment and to help develop more personalized medicine. It is a long-term observational study following patients through their lifetime with active or passive follow-up. Participants provide blood samples up to four times a year during regular care visits. Extra tissue is collected during standard surgery, and additional tumor samples may be taken during planned biopsies. Bone marrow may be sampled up to four times a year with careful needle repositioning. Other biological samples like saliva, sputum, urine, feces, hair, and skin swabs are also collected. Alongside sample collection, participants complete surveys about demographics, medical and family history, cancer risk factors, quality of life, and quality of care. During the study, participants are followed periodically even after initial data collection. Researchers review medical charts and assess quality of life through questionnaires. The primary outcome is the number of biospecimens collected and linked to clinical data over up to 21 years. This helps build a resource for future studies matching patients to new research opportunities.
CONDITIONS
Brief Title
Norris ORIEN Total Cancer Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Must be registered for outpatient or inpatient care at University of Southern California Norris
- Able to understand and sign the informed consent, subject's bill of rights, HIPAA, and research authorization in English or Spanish
You will not qualify if you...
- Not registered as a patient for outpatient or inpatient care at University of Southern California Norris
- Unable to understand or sign the informed consent, subject's bill of rights, HIPAA, and research authorization in English or Spanish
AI-Screening
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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 21 years
Participants undergo collection of blood during regular care visits up to 4 times a year. Additional biological samples such as saliva, sputum, urine, feces, hair, and surface skin swabs may also be collected for analysis. Participants provide survey or questionnaire data on demographics, medical and family history, cancer risk factors, and quality of life.
Up to 4 visits per year
Duration - As needed during care
Participants may undergo additional tumor sampling during planned diagnostic biopsies and extra tissue collection during standard of care surgery. Bone marrow biopsies for research may occur up to 4 times per year with up to 3 needle repositionings during each procedure.
Visits as needed depending on clinical procedures
Duration - Ongoing after active collection ends
After completion of active data and sample collection, participants are followed up periodically to monitor clinical outcomes and maintain the biospecimen repository linkage.
Periodic follow-up visits
Trial Site Locations
Total: 1 location
1
USC / Norris Comprehensive Cancer Center
Los Angeles, California, United States, 90033
Actively Recruiting
Research Team
M
Melissa Woodhouse, MHA, MPH
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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