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Repositories and other initiatives

In this section, we are studying data sharing platforms, repositories and indeed any other initiative.

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01

STATUS OF SHARING OF INDIVIDUAL PARTICIPANT DATA FROM CLINICAL TRIALS, USE OF SHARED DATA AND IMPACT OF RESEARCH OUTPUTS OF SHARING DATA

To explore the impact of early clinical trial data initiatives in terms of five outcome domains: status of intent to share data, status of data sharing, use of shared data and impact of research outputs from shared data.
Protocol / Paper

02

ATTENTION AND IMPACT OF SHARING INDIVIDUAL PARTICIPANT DATA FROM CLINICAL TRIALS: A CROSS SECTIONAL ANALYSIS OF PUBLISHED RE-USE FROM 3 MAJOR REPOSITORIES

Les médias sociaux numériques

Randomized clinical trials data sharing policies should have an evaluation component. Our main objective was to assess the impact of published re-uses from RCTs using media attention (Altmetric) and citation rates.

Protocol / Paper 

Loupe

03

INFERENTIAL REPRODUCIBILITY OF THERAPEUTIC RESEARCH: A CROSS-SECTIONAL STUDY OF RANDOMIZED CONTROLLED TRIALS AVAILABLE ON MAJOR DATA-SHARING PLATFORMS

This registered report introduces a cross-sectional study aiming to assess inferential reproducibility (qualitatively similar conclusions can be drawn from a reanalysis of the original trials) for main RCTs available on major data-sharing platforms.

Protocol / Work in progress, in principle acceptance at Royal Society Open Science