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Low awareness of kidney disease remains a challenge for clinical trial recruitment


In this feasibility study, researchers found low awareness of kidney disease for many participants and a challenge in recruiting vulnerable populations. Visual Abstract for “A National Registry for People With All Stages of Kidney Disease: The National Kidney Foundation (NKF) Patient Network” by Lesley A. Inker et al (AJKD, 2022). Credit: Inker et al (AJKD, 2022)

Among 80 participants of the NKF Patient Network, a national U.S. kidney disease registry, 60% were not aware of their kidney function level.

The NKF Patient Network (NKFPatientNetwork.org) is a nationwide kidney disease patient registry created to improve the lives of people with kidney disease through research, , and drug development. The network has a secure portal for participants to share their experiences and data, and for providers to upload upon patient consent. The network also offers individualized education and support.

In this feasibility study, published in the American Journal of Kidney Diseases (AJKD), researchers found low awareness of kidney disease for many participants and a challenge in recruiting vulnerable populations. These are short-term goals of the network following the national launch in February 2021. Overall, the network will facilitate real-world data collection to inform the development of patient-centered research, care, and treatments for people with .


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More information:
Lesley A. Inker et al, A National Registry for People With All Stages of Kidney Disease: The National Kidney Foundation (NKF) Patient Network, American Journal of Kidney Diseases (2022). DOI: 10.1053/j.ajkd.2022.07.016

Provided by
National Kidney Foundation

Citation:
Low awareness of kidney disease remains a challenge for clinical trial recruitment (2022, September 30)
retrieved 30 September 2022
from https://medicalxpress.com/news/2022-09-awareness-kidney-disease-clinical-trial.html

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