Plain-English translation of NCT03720197 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Type 1 Diabetes Mellitus research guide →This is a research registry—a database where people with type 1 diabetes share their health information and experiences. The study has three phases that gradually collect more detailed information: first, basic questions about your diabetes and treatment (about 10 minutes); second, deeper questions about low blood sugar episodes and, if you're willing and live in Quebec or Alberta, your recent blood and urine test results; and third, questions about sleep, mood, physical activity, and how different diabetes technologies help you manage your condition.
Researchers want to build a clear picture of how type 1 diabetes is managed in Canada today, what challenges people face with low blood sugar episodes, and how different treatments and technologies are working in real life. This information will help doctors better understand and treat type 1 diabetes.
You likely qualify if…
You likely don't qualify if…
Participation happens in phases. In phase 1, you'll answer a brief 10-minute questionnaire about your diabetes and treatment. If you use a continuous glucose monitor and agree, you can share your latest report. In phase 2, you'll answer more detailed questions about low blood sugar episodes, and if you live in Quebec or Alberta, you can optionally provide recent blood and urine test results and your medication list. In phase 3, you'll share information about your sleep, mood, physical activity, diet, and how helpful different diabetes technologies have been for you—and you can optionally wear a step counter and have your waist measured.
AI-generated summary from trial data · Jun 2, 2026 · Not medical advice
Canada