A protocol for a systematic review investigating the factors influencing the statistical planning, design, conduct, analysis and reporting of trials

Marina Zaki, Marie Galligan, Lydia O'Sullivan, Declan Devane, Eilish McAuliffe

Research output: Contribution to a Journal (Peer & Non Peer)Review articlepeer-review

1 Citation (Scopus)

Abstract

Trials can be defined as prospective human research studies to test the effectiveness and safety of interventions, such as medications, surgeries, medical devices and other interventions for the management of patient care. Statistics is an important and powerful tool in trials. Inappropriately designed trials and/or inappropriate statistical analysis produce unreliable results, with limited clinical use. The aim of this systematic literature review is to identify, describe and synthesise factors contributing to or influencing the statistical planning, design, conduct, analysis and reporting of trials. This protocol will describe the methodological approach taken for the following: conducting a systematic and comprehensive search for relevant articles, applying eligibility criteria for the inclusion of such articles, extracting data and information, appraising the quality of the articles, and thematically synthesizing the data to illuminate the key factors influencing statistical aspects of trials.

Original languageEnglish
Article number36
JournalHRB Open Research
Volume3
DOIs
Publication statusPublished - 2020

Keywords

  • Clinical trials
  • protocol
  • statistics
  • systematic review

Fingerprint

Dive into the research topics of 'A protocol for a systematic review investigating the factors influencing the statistical planning, design, conduct, analysis and reporting of trials'. Together they form a unique fingerprint.

Cite this