Trial Registry Listings
We create plain language study listings that are easy for patients to understand
Empower patients and study staff from the start, with clinical trial information that supports understanding and communication.
The Problem
Regulatory clinical trial registries are difficult to understand.
Most regulatory registries like ClinicalTrials.gov provide listings of clinical trials that are difficult for patients and the public to understand. Trial descriptions at ClinicalTrials.gov are extremely difficult to read, requiring 18 years of education on average to understand them.1
CISCRP's Solution
Using your study protocol, we create a plain language study registry posting that meets the specific requirements of ClinicalTrials.gov.
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Simple and visually engaging study information for posting on registry and trial-finder websites
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Empower patients and study staff by easing the communication burden from the very beginning of study conduct
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Establish consistency and improve efficiency by utilizing the plain language study title, purpose, condition, and inclusion/exclusion criteria
- Edwards, Kimbra. “Examining the Current Value of ClinicalTrials.gov Listings for Patients and the Public.” Applied Clinical Trials, 2022, https://www.appliedclinicaltrialsonline.com/view/examining-the-current-value-of-clinicaltrials-gov-listings-for-patients-and-the-public.