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  • 5th International Clinical Trials Methodology Conference (ICTMC 2019)
    5th International Clinical Trials Methodology Conference (ICTMC 2019)
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    Building on the success of the 2017 International Clinical Trials Methodology Conference, this event promises to be a unique opportunity for those working in clinical trials (trialists, methodologists, clinicians and allied health professionals) to meet and discuss the current issues within trials and trials methodology. The event will showcase the very latest in trials methodology…

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  • MiRoR Challenge award winners announced in Barcelona
    MiRoR Challenge award winners announced in Barcelona
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    This activity aimed to initiate entrepreneurial and innovative skills among students. Divided into 4 groups, students worked in teams over 1 year (March 2018 – March 2019) to propose a new intervention that could transform the way research is planned, conducted or reported. They had several opportunities to receive feedback from the consortium via video-conferences or face-to-face meetings…

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  • Project output – seminar by one of our fellows in Madrid
    Project output – seminar by one of our fellows in Madrid
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    On March 5, 2019 our fellow David Blanco gave a 2h seminar for professors and doctoral students at the Department of Basic Psychology and Methodology of the Universidad Autónoma de Madrid (UAM) focusing on the content and progress of his PhD project under the MiRoR project, “Assessing interventions to improve adherence to reporting guidelines”. After…

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  • MiRoR fellow awarded ASA’s Norman Breslow Prize (Statistics in Epidemiology)
    MiRoR fellow awarded ASA’s Norman Breslow Prize (Statistics in Epidemiology)
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    We are very proud to announce that Vo Tat Thang, MiRoR research fellow at the University of Ghent and University Paris Descartes, was awarded the Norman Breslow Prize from the Statistics in Epidemiology section of the American Statistics Association (ASA) for his paper on “Rethinking meta-analysis: addressing problems of non-transportability when combining treatment effects across…

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  • Exploring the endorsement of STROBE and its extensions by journals
    Exploring the endorsement of STROBE and its extensions by journals
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    In a previous post detailing my time with the EQUATOR Network, I spoke about my work on the STrengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement. STROBE is one of the original “core” reporting guidelines which provides guidance on reporting observational studies. As an overwhelming majority of health research is observational (i.e., not manipulating…

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  • Biostatnet 4th General Meeting
    Biostatnet 4th General Meeting
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    The 4th General Meeting of the National Biostatistics Network will be held in Santiago de Compostela on January 25-26, 2019 under the theme Biostatistics and Data Science: challenges and opportunities. The main aims of this meeting are to reinforce the links between members of the BIOSTATNET family and to allow members of the network to…

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  • Symposium on the Efficiency and Analysis of Trials using Routine Data
    Symposium on the Efficiency and Analysis of Trials using Routine Data
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    Innovative designs for randomized controlled trials (RCTs) utilising existing health data are increasingly used in healthcare intervention research. This includes trial designs that use existing data sources (randomized registry trials, administrative health record trials, and electronic health record trials) as well as Trials within Cohorts (TwiCs) designs. How efficient are these trial designs? How should…

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  • MiRoR project highlight – finding best research
    MiRoR project highlight – finding best research
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    HOW DO YOU MEASURE THE QUALITY OF RESEARCH AND WHAT DOES IT CHANGE IN YOUR LIFE? Clinical guidelines and systematic reviews are synthesis of all the existing knowledge concerning a clinical relevant question; they are done with a precise and well established methodology. Synthesizing the results of high quality studies is the best way to…

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  • Biomedical editors survey on peer-review
    Biomedical editors survey on peer-review
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    Our fellow Cecilia Superchi is calling for biomedical editors to participate in her study aiming at investigating how they define the quality of a peer-review report. This survey constitutes the second part of her research project: in a first phase she conducted a systematic review to analyze the existing tools used to assess the quality of peer-review…

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  • Tell the FDA to identify and punish organisation and people who are not reporting clinical trial results
    Tell the FDA to identify and punish organisation and people who are not reporting clinical trial results
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    The FDA Amendment Act 2007 says that lots of clinical trials in the US should be registered on ClinicalTrials.gov and report results information there within 12 months of the end of the trial. AllTrials’s FDAAA TrialsTracker shows that 628 clinical trials have broken this law since the first trials became due in January this year. Information on what…

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This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 676207
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