Deciding to participate in a clinical trial can be a difficult decision.
Deciding on behalf of a child is often even more difficult.
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Over 90% of study participants want to know
the results of their clinical trials yet only 8% report
hearing from the study staff after the trial has ended.
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The Center for Information and Study on Clinical Research Participation (CISCRP) is an independent non-profit organization dedicated to educating and informing the public and patients about clinical research. CISCRP also provides information and resources to help research and health professionals better serve their patients and study volunteers. LEARN MORE...
Visit the Store to explore CISCRP's extensive library of engaging tools and resources that empower patients and the public.
