Abstract

BackgroundThe Plan-Do-Study-Act (PDSA) cycle is a commonly used improvement process in health care settings, although its documented use in pragmatic clinical research is rare. A recent pragmatic clinical research study, called the Strategies and Opportunities to STOP Colon Cancer in Priority Populations (STOP CRC), used this process to optimize the research implementation of an automated colon cancer screening outreach program in intervention clinics. We describe the process of using this PDSA approach, the selection of PDSA topics by clinic leaders, and project leaders’ reactions to using PDSA in pragmatic research.MethodsSTOP CRC is a cluster-randomized pragmatic study that aims to test the effectiveness of a direct-mail fecal immunochemical testing (FIT) program involving eight Federally Qualified Health Centers in Oregon and California. We and a practice improvement specialist trained in the PDSA process delivered structured presentations to leaders of these centers; the presentations addressed how to apply the PDSA process to improve implementation of a mailed outreach program offering colorectal cancer screening through FIT tests. Center leaders submitted PDSA plans and delivered reports via webinar at quarterly meetings of the project’s advisory board. Project staff conducted one-on-one, 45-min interviews with project leads from each health center to assess the reaction to and value of the PDSA process in supporting the implementation of STOP CRC.ResultsClinic-selected PDSA activities included refining the intervention staffing model, improving outreach materials, and changing workflow steps. Common benefits of using PDSA cycles in pragmatic research were that it provided a structure for staff to focus on improving the program and it allowed staff to test the change they wanted to see. A commonly reported challenge was measuring the success of the PDSA process with the available electronic medical record tools.ConclusionUnderstanding how the PDSA process can be applied to pragmatic trials and the reaction of clinic staff to their use may help clinics integrate evidence-based interventions into their everyday care processes.Trial registrationClinicaltrials.gov NCT01742065. Registered October 31, 2013.

Highlights

  • The Plan-Do-study the data collected (Study)-Act (PDSA) cycle is a commonly used improvement process in health care settings, its documented use in pragmatic clinical research is rare

  • A pragmatic clinical trial called the Strategies and Opportunities to STOP Colon Cancer in Priority Populations (STOP colorectal cancer (CRC)) recently used this process to optimize the implementation of a cancer screening outreach program

  • This paper describes how our study used PDSA in pragmatic research to assist in improving implementation of the planned intervention; this technique could have broader applications in a wide range of quality improvement activities and other types of pragmatic trials

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Summary

Introduction

The Plan-Do-Study-Act (PDSA) cycle is a commonly used improvement process in health care settings, its documented use in pragmatic clinical research is rare. A recent pragmatic clinical research study, called the Strategies and Opportunities to STOP Colon Cancer in Priority Populations (STOP CRC), used this process to optimize the research implementation of an automated colon cancer screening outreach program in intervention clinics. The Plan-Do-Study-Act (PDSA) cycle is a commonly used improvement process in health care settings that might have untapped potential for pragmatic research. A pragmatic clinical trial called the Strategies and Opportunities to STOP Colon Cancer in Priority Populations (STOP CRC) recently used this process to optimize the implementation of a cancer screening outreach program. While PDSA cycles are commonly used in clinical care, few clinical research trials have documented its use for implementation. The PDSA cycle may prove useful in adapting and implementing research-based interventions, where its incorporation into every-day care is a central question

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