The Center for Information and Study on Clinical Research Participation, Inc.’s (CISCRP) core mission is to provide accessible, relevant, useful, high-quality educational resources, programs, and services that increase awareness and understanding of the clinical research process; recognize and appreciate the unprecedented gift of participation in clinical trials; enhance and enrich the participation experience for patients and their families; and promote engagement and partnership between clinical research professionals, patients, and the public.
Educating and Empowering Patients and the Public to be Viewed and Engaged as Partners in Clinical Research
We strive to educate and help patients, their family members, and members of the general public that are interested in clinical research understand the process and what it means to be a clinical research participant. We help locate ongoing clinical trials through our free service called Search Clinical Trials, provide a wide variety of clinical research resources, and honor those who have participated in clinical research.
We help professionals better understand the study volunteer with facts and figures, polls, surveys and other resources, while promoting a greater awareness of clinical trials. We are uniquely positioned to provide several plain language services as well. Additionally, we offer a library of clinical research content—brochures, posters, videos—and other materials to license, sponsor, or co-develop.
Meet the CISCRP Team.
Learn about our services and programs.
Join the CISCRP team.
Dominantly Inherited Alzheimer’s Disease Brochure
Expanded Registry Flyer (English)
Enfermedad de Alzheimer de herencia dominante
Expanded Registry Flyer (Spanish)
Forgetting the Little Things
Concerned About Memory Loss?
Click on the resources listed below to view the full versions of LCI’s materials.