CISCRP offers a portfolio of services to support patient engagement, clinical research education, and clinical trial participation for study volunteers, clinical research stakeholders, and sponsor organizations. As an independent, neutral, non-profit organization dedicated to patient outreach and education, CISCRP is uniquely positioned to assist with a variety of activities including developing lay language clinical trial summaries, organizing and running patient advisory boards, conducting research to better understand public perceptions about research, and finding clinical trials.
CISCRP offers services for plain language, health literacy, informed consent, pediatric trial results, and more.
CISCRP conducts research studies to understand public and patient perceptions, motivations, and experiences with clinical research. Patient and care partner advisory boards, workshops, and custom research projects are also offered.
CISCRP has a library of award-winning educational clinical research content available to license.
As a nonprofit with industry and community connections, CISCRP is uniquely qualified to help you develop, advertise, and present webinars to your target audience.
CISCRP implements a large-scale print & digital media campaign that builds awareness on the importance of diverse clinical trial participation.
CISCRP hosts and partners with other organizations to hold educational events, including webinars, grassroots community events, and more.
We offer a free service for patients, caregivers, and the public where we help identify clinical trials based on their healthcare criteria.
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.