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Complementary Options for Symptom Management In Cancer COSMIC Assessing Benefits and Harms of Cannabis and Cannabinoid Use Among Cancer Patients Treated in Community Oncology Clinics
Led by Wake Forest University Health Sciences · Updated on 2026-03-17
2000
Participants Needed
467
Research Sites
N/A
Total Duration
On this page
Sponsors
W
Wake Forest University Health Sciences
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying adults newly diagnosed with breast, colorectal, melanoma, non-Hodgkin lymphoma, or non-small cell lung cancer who are planning to receive systemic cancer therapies such as chemotherapy and immune checkpoint inhibitors ICIs. The study aims to understand how cannabis and cannabinoid use relates to cancer-related symptoms over one year. This observational research includes patients treated in community oncology clinics and is sponsored by Wake Forest University Health Sciences. Participants complete surveys and allow medical record reviews throughout the study. The study tracks cannabis and cannabinoid use as well as perceived benefits, harms, and adverse effects monthly for 12 months following enrollment. An optional sub-study is available at select sites for patients with non-small cell lung cancer receiving specific chemotherapy with ICIs. During the study, participants fill out monthly surveys about their symptoms and cannabis use. Researchers also review medical records to assess cancer-related symptoms and treatment progress. The main measure is cancer-related symptoms assessed monthly for up to one year. Secondary measures include cannabis use patterns and adverse effects. Participation involves ongoing survey completion and record review, with the total study duration lasting 12 months post-enrollment.
CONDITIONS
Brief Title
Assessing Benefits and Harms of Cannabis/Cannabinoid Use Among Cancer Patients Treated in Community Oncology Clinics
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older with newly diagnosed breast, colorectal, melanoma, non-Hodgkin lymphoma, or non-small cell lung cancer
- Planned treatment with systemic chemotherapy and/or immune checkpoint inhibitor therapy targeting PD-1, PD-L1, or CTLA-4
- Able to understand English or Spanish for survey completion
- Have a working email address and willing to complete online surveys
- Completed Self-Reported Screening Survey and eligible for enrollment
- Reside in the United States as reported by the participant
- Life expectancy of at least 6 months according to treating provider
- Enrollment allowed up to start of Cycle 2 treatment if not engaged before treatment start
- Optional sub-study: receiving treatment at select centers, diagnosed with non-small cell lung cancer, and planning specific chemotherapy with ICIs
You will not qualify if you...
- Currently enrolled in an interventional supportive treatment trial for cancer symptoms
- Known pregnancy
- Received systemic therapy for prior cancers
- Enrolled in hospice
- Optional sub-study exclusion: use of chronic steroids or immunomodulatory agents (except pre-medications), history of HIV, hepatitis B or C
Research Team
K
Karen Craver
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