CONSORT extension for reporting N-of-1 trials (CENT) 2015 Statement

J Clin Epidemiol. 2016 Aug:76:9-17. doi: 10.1016/j.jclinepi.2015.05.004. Epub 2015 Aug 10.

Abstract

N-of-1 trials provide a mechanism for making evidence-based treatment decisions for an individual patient. They use key methodological elements of group clinical trials to evaluate treatment effectiveness in a single patient, for situations that cannot always accommodate large-scale trials: rare diseases, comorbid conditions, or in patients using concurrent therapies. Improvement in the reporting and clarity of methods and findings in N-of-1 trials is essential for reader to gauge the validity of trials and to replicate successful findings. A Consolidated Standards of Reporting Trials (CONSORT) extension for N-of-1 trials (CENT 2015) provides guidance on the reporting of individual and series of N-of-1 trials. CENT provides additional guidance for 14 of the 25 items of the CONSORT 2010 checklist, recommends a diagram for depicting an individual N-of-1 trial, and modifies the CONSORT flow diagram to address the flow of a series of N-of-1 trials. The rationale, development process, and CENT 2015 checklist and diagrams are reported in this document.

Keywords: CENT; CONSORT; N-of-1; Reporting guideline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomedical Research / standards*
  • Clinical Trials as Topic / standards*
  • Guidelines as Topic*
  • Humans
  • Publishing / standards*
  • Research Design / standards*
  • Research Report / standards*
  • Terminology as Topic*