🏛️ Verified NIH Record • Updated 2026-08-10

Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials (NCT07390435)

🟢 Recruiting Interventional Protocol 📊 Observational Clinical Research Sponsor: Canadian Cancer Trials Group

🩺 Plain-English Summary (8th-Grade Level)

This study is being done to answer the following question: Are patients on a clinical trial willing to provide answers to questions about their social, economic, and environmental factors-sometimes called social determinants of health-which affect people's health experiences and access to care. These factors may include income, education, employment, housing, social supports, and experiences with discrimination or stress. Participation will help researchers better understand barriers to participating in clinical trials and access to health care.

Who can join: Review the eligibility criteria below.

Location: Arthur J.E. Child Comprehensive Cancer Centre — Calgary, Alberta

Age range: 18 Years

🧪 Interventions in This Study

  • Social Determinants of Health Questionnaire (OTHER)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (11 Sites)

  • Arthur J.E. Child Comprehensive Cancer Centre — Calgary, Alberta
  • BCCA - Kelowna — Kelowna, British Columbia
  • BCCA - Prince George — Prince George, British Columbia
  • BCCA - Vancouver — Vancouver, British Columbia
  • BCCA - Victoria — Victoria, British Columbia
  • Regional Health Authority B, Zone 2 — Saint John, New Brunswick
  • Kingston Health Sciences Centre — Kingston, Ontario
  • Odette Cancer Centre — Toronto, Ontario
  • CHA-Hopital Du St-Sacrement — Québec, Quebec
  • Allan Blair Cancer Centre — Regina, Saskatchewan
  • Saskatoon Cancer Centre — Saskatoon, Saskatchewan

📞 Contact the Study Coordinator

Phone: (613) 533-6430

Email: ajohnson@ctg.queensu.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 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 § 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.

Explore by condition: All Cancer clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗