Clinical Trial Sites
Help increase minority involvement in clinical trials by building relationships with providers and encouraging them to raise patient awareness about clinical trial opportunities.
Download the distribution guide to learn how MIMICT can be used to overcome provider concerns about referring patients to clinical trials.
This distribution guide provides lupus clinical trial sites with resources on:
- how to promote the education course and patient materials contained in the education toolkit,
- how to support and create connections with providers as recruitment partners, and
- how to customize the distribution toolkit with information on the site’s specific clinical trial.
Tailor MIMICT customizable materials to facilitate relationship building with healthcare providers by educating them about the value of clinical trials to their patients’ treatment outcomes.
These informational materials can be customized for use at individual lupus clinical trial sites.
This project was supported by Grant Numbers 1 CPIMP171138 and 1 CPIMP181166 from the U.S. Department of Health and Human Services, Office of Minority Health (HHS, OMH). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the HHS, OMH.