+1 877 705 191424 / 7
HIPAA Compliant
ISO 27001 Certified

Actively Recruiting

Age: 18Years +
All Genders
ID06418204

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here