Health Communication Projects
CISCRP can translate the following documents:
CISCRP will translate the technical, scientific results of clinical trials into plain language.
Informed consent documents:
CISCRP will create a general template for ICFs (including graphic design) that can be available to study teams or translate study-specific ICFs into plain language.
Working from scientific manuscripts, CISCRP will create a document that is accessible to patients, patient advocacy organizations, and the public.
Working from your manuscript, CISCRP will draft an abstract for journal submission.
Patient education brochures:
Working from your protocol or the informed consent document, CISCRP will develop a patient education brochure to complement your informed consent process.
CISCRP will provide plain language summaries of proposed research, written in a form suitable for disclosure under the Freedom of Information Act, for grant applications or ethics submissions.
Using the source documents provided by you, CISCRP will work with a Health Literacy Lawyer who is an expert in designing effective, user-friendly communications that both comply with law and are easily understandable to patients and the public.
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