๐๏ธ Verified NIH Record โข Updated 2026-04-24
Comparative Effectiveness Trial of Two Supportive Cancer Care Delivery Models for Adults With Cancer (NCT05297734)
๐ข Recruiting Observational / Diagnostic ๐ง Behavioral & Psychological Program Sponsor: Stanford University
๐ฉบ Plain-English Summary (8th-Grade Level)
This cluster-randomized comparative effectiveness trial compares a technology-based supportive cancer care (SCC) approach with a redesigned team-based supportive cancer care (SCC) approach.
Who can join: Review the eligibility criteria below.
Location: University of Alabama at Birmingham โ Birmingham, Alabama
Age range: 18 Years
๐งช Interventions in This Study
- Receive technology-based supportive cancer care (OTHER)
- Receive redesigned team-based supportive cancer care (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (17 Sites)
- University of Alabama at Birmingham โ Birmingham, Alabama
- University of South Alabama โ Mobile, Alabama
- Beckman Research Institute of City of Hope โ Duarte, California
- VA Medical Center, Fresno โ Fresno, California
- Santa Clara Valley Medical Center โ Fruitdale, California
- St Jude Heritage Medical Group โ Fullerton, California
- Oncology Institute for Hope and Innovation โ Los Angeles, California
- Sacramento VA Medical Center - VA Northern California Health Care System โ Mather, California
- Pacific Cancer Care โ Monterey, California
- VA Palo Alto โ Palo Alto, California
- Zuckerberg San Francisco General โ San Francisco, California
- Kaiser Foundation Research Institute โ San Francisco, California
- University of San Francisco โ San Francisco, California
- San Francisco VA Medical Center โ San Francisco, California
- Spark M. Matsunaga VA Medical Center โ Honolulu, Hawaii
- North Las Vegas VA Medical Center โ Las Vegas, Nevada
- George E. Wahlen Department of Veterans Affairs Medical Center โ Salt Lake City, Utah
๐ Contact the Study Coordinator
Phone: (650) 723-4000
Email: manalip@stanford.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.