Building a national registry for pain assessment
Part of Pain clinical trials.
This study is building a national database called a registry to better understand and treat pain across all ages. If you join, you'll provide information about your pain through digital questionnaires, which will help improve pain care for everyone.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have been diagnosed with pain, either lasting less than 3 months (acute) or 3 months or longer (chronic).
- You must have been referred to a pain clinic or a specialized pain assessment service.
- You need to be able to answer questions on a digital device (computer, tablet, or smartphone) in German, French, Italian, or English. For children, a parent or guardian can help.
- You must be in a stable health condition (no immediate life-threatening emergency).
- For minors, a parent or legal guardian must agree to participate and can provide consent if needed.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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