Rare Diseases Clinical Research Network Contact Registry

In today's world, Rare Diseases Clinical Research Network Contact Registry has become a topic of great relevance and interest to a wide spectrum of society. The importance of Rare Diseases Clinical Research Network Contact Registry has left its mark on history and is present in people's daily lives. From its origins to the present, Rare Diseases Clinical Research Network Contact Registry has been the subject of debate and analysis in different areas, from politics to science, including culture and technology. For this reason, it is essential to understand the impact that Rare Diseases Clinical Research Network Contact Registry has on our lives and in the global context. In this article, we will explore in depth the importance of Rare Diseases Clinical Research Network Contact Registry and its implications in the contemporary world.

The Rare Diseases Clinical Research Network (RDCRN) Contact Registry[1][2] is a patient contact registry started in 2004 and sponsored by the National Institutes of Health (NIH).[3][4] The RDCRN Contact Registry collects and stores the contact information of people who want to participate in RDCRN-sponsored research or learn more about RDCRN research. It connects patients with researchers in order to advance rare disease research.[5][6]

The Rare Diseases Clinical Research Network (RDCRN)[7] is a U.S.-based research network funded by the NIH. It fosters research to better understand, diagnose, and treat rare diseases. Its 20 consortia—teams of scientists, physicians, and patients—each study a group of related rare diseases. Established by Congress under the Rare Diseases Act of 2002, the RDCRN is an initiative of the Office of Rare Diseases Research at the NIH's National Center for Advancing Translational Sciences. Future research may produce helpful information for those with rare diseases.

Individuals who are 18 years of age and older and have a rare disease, are a caregiver for someone with a rare disease, or an unaffected individual can join the RDCRN registry. The contact registry collects basic data (i.e. contact information, diagnosis, medical history) to be stored in a secure, computerized database hosted by the RDCRN's Data Management and Coordinating Center based at Cincinnati Children's Hospital Medical Center.

Function

The registry collects and maintains the contact information of people who want to:

  • Receive information about RDCRN's rare diseases research
  • Learn about opportunities to participate in RDCRN research.

It allows patients and others to connect with research teams and patient advocacy groups focused on particular diseases. data about individuals who are interested in receiving information about rare disease research and opportunities for research participation. The registry supports the dissemination of information relevant to the RDCRN community. It also offers RDCRN investigators and patient advocacy groups access to data that will help them assess the feasibility of conducting a proposed study.

Funding

The RDCRN Contact Registry is operated by the Rare Diseases Clinical Research Network which is funded by the National Institutes of Health and led by the National Center for Advancing Translational Sciences through its Office of Rare Diseases Research. It is governed by the RDCRN Contact Registry Oversight Committee. The contact registry is hosted and maintained by the RDCRN's Data Management and Coordinating Center at Cincinnati Children's Hospital Medical Center.

References

  1. ^ "RDCRN Launches Contact Registry to Connect Patients, Researchers and Advance Rare Disease Research". Rare Diseases Clinical Research Network. Retrieved 2022-03-15.
  2. ^ "RDCRN Contact Registry". Rare Diseases Clinical Research Network. Retrieved 2022-03-15.
  3. ^ Groft, Stephen C.; Gopal-Srivastava, Rashmi (2013). "A model for collaborative clinical research in rare diseases: experience from the Rare Disease Clinical Research Network program" (PDF). Clinical Investigation. 3 (11): 1015–1021. doi:10.4155/cli.13.101.
  4. ^ Richesson, Rachel L.; Sutphen, Rebecca; Shereff, Denise; Krischer, Jeffrey P. (July 2012). "The Rare Diseases Clinical Research Network Contact Registry update: Features and functionality". Contemporary Clinical Trials. 33 (4): 647–656. doi:10.1016/j.cct.2012.02.012. PMC 3652679. PMID 22405970.
  5. ^ Merkel, Peter A.; Manion, Michele; Gopal-Srivastava, Rashmi; Groft, Stephen; Jinnah, H. A.; Robertson, David; Krischer, Jeffrey P. (December 2016). "The partnership of patient advocacy groups and clinical investigators in the rare diseases clinical research network". Orphanet Journal of Rare Diseases. 11 (1): 66. doi:10.1186/s13023-016-0445-8. ISSN 1750-1172. PMC 4870759. PMID 27194034.
  6. ^ Richesson, R. L.; Lee, H. S.; Cuthbertson, D.; Lloyd, J.; Young, K.; Krischer, J. P. (January 2009). "An automated communication system in a contact registry for persons with rare diseases: Scalable tools for identifying and recruiting clinical research participants". Contemporary Clinical Trials. 30 (1): 55–62. doi:10.1016/j.cct.2008.09.002. PMC 2640948. PMID 18804556.
  7. ^ "Home | Rare Diseases Clinical Research Network". rdcrn.org. Retrieved 2022-03-15.
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