Including People with Lived Experience of Pain in the Research Process: Do It Early and Often

Kayt Sukel / RELIEF (December 13, 2020)

“More and more, we see the value of taking a more patient-centered approach, at every step of the research process,” said Captain Robyn Bent, director of the ongoing Patient-Focused Drug Development (PFDD) initiative, which was established at the US Food and Drug Administration (FDA) in 2012. “In the early stages, that patient input can help researchers understand the impact of the disease and existing treatments, helping us better understand what we need to measure to see if something has worked or not. Once we get to clinical trials, patients can help us understand what aspects of those trials need to be better tailored to fit the needs of the people who will end up participating in those trials. And once a treatment is available, patients can help us understand how to best communicate information to both patients and doctors to facilitate shared decision-making.”

Kayt Sukel. Including People with Lived Experience of Pain in the Research Process: Do It Early and Often.

Read the article in RELIEF here.

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