This resource, in support of “Reporting Data (Trials),” aims to promote implementation and use of the CONSORT-PRO Extension for trials where PROs are primary or key secondary outcomes. The template is also recommended for use where PROs are exploratory outcomes.
This powerpoint, in support of “Reporting Data (Trials),” describes the recommended information about PRO endpoints to include in clinical trial publications. Presented by: Melanie Calvert, PhD; Michael Brundage, MD, MSc
The “Reporting Data (Trials): Handbook Chapter” resource is an excerpt of the PROTEUS-Trials Handbook summarizing the recommendations for reporting PRO components of research studies. View the entire Handbook here (US version) or here (UK version).
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
This checklist, in support of “Reporting Data (Trials),” lists the recommended PRO content to include in each section of a clinical trial publication.
This article, in support of “Reporting Data (Trials),” describes the development of the CONSORT PRO (Consolidated Standards of Reporting Trials) extension, which recommends the key PRO information to include in clinical trial publications.
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