AI Article Synopsis

  • There is a growing interest in involving patients as partners in clinical trials for pain treatments, but there is currently no specific guidance on how to do this effectively.
  • This review discusses historical and current perspectives on patient engagement in clinical research, including how regulatory and funding agencies are beginning to incorporate patient input in their decision-making.
  • The authors highlight key practices for recruiting and engaging patients, the benefits and challenges of these partnerships, and outline factors that impact patient engagement in pain-related studies, as well as gaps for future research to improve patient-centered clinical research.

Article Abstract

The interest and the rationale for meaningful engagement of patients as partners in clinical trials of pain treatments has been increasing. No specific guidance on patient engagement for pain research studies currently exists; thus, the goal of this narrative review was to provide a historical perspective and a current evaluation of the literature on engaging patients as partners in clinical studies in general and in pain-related studies more specifically. We described how regulatory and funding agencies have developed approaches to incorporate input from patients and patient partners in their decision-making processes. We provided an overview on key practices of patient recruitment and engagement as partners in clinical research and highlighted the perceived benefits and challenges of such partnerships. We summarized factors that can facilitate or hinder meaningful patient engagement in clinical trials of pain treatments and outlined gaps that future research should address to optimize patient-centered clinical research.

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Source
http://dx.doi.org/10.1097/j.pain.0000000000002600DOI Listing

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