This powerpoint, a resource supporting “Analyzing Data (Trials),” provides information on PRO data analysis. Presented by: Corneel Coens, MSc
This powerpoint, in support of “Selecting Measures (Trials),” provides a detailed description of the minimum standards for selecting PRO measures for research studies. Presented by: Bryce R. Reeve, PhD
This powerpoint, in support of “Selecting Measures (Trials),” provides an overview of minimum standards for selecting PRO measures for research studies. Presented by: Bryce R. Reeve, PhD
This checklist, in support of “Displaying Results (Trials),” summarizes the recommendations for visualization of PRO data to clinicians and researchers in, for example, research publications.
This checklist, in support of “Displaying Results (Trials),” summarizes the recommendations for visualization of PRO data to patients in educational materials and decision aids.
This video, in support of “Selecting Measures (Trials),” provides an in-depth discussion of the minimum standards for selecting PRO measures for research studies. Presented by: Bryce B. Reeve, PhD
This video, in support of “Selecting Measures (Trials),” provides an overview of the minimum standards for selecting PRO measures for research studies. Presented by: Bryce B. Reeve, PhD
Describes the founding of PROTEUS and its work to guide and strengthen the use of PROs in clinical trials. (Clin Trials 2022)
This handbook (US Version) accompanies a series of powerpoints about PROTEUS-Trials and the tools and resources available to optimize the use of patient-reported outcomes in clinical trials.
This handbook (UK Version) accompanies a series of powerpoints about PROTEUS-Trials and the tools and resources available to optimize the use of patient-reported outcomes in clinical trials.
This video, in support of “Reporting Data (Trials),” discusses in detail the recommended information about PRO endpoints to include in clinical trial publications. Presented by: Melanie Calvert, PhD; Michael Brundage, MD, MSc
This video, in support of “Reporting Data (Trials),” provides an overview of recommended information about PRO endpoints to include in clinical trial publications.” Presented by: Melanie Calvert, PhD; Michael Brundage, MD, MSc
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