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16/07/2024 Reporting of surrogate endpoints in randomised controlled trial reports (CONSORT-Surrogate): extension checklist with explanation and elaboration 16/07/2024 Reporting of surrogate endpoints in randomised controlled trial protocols (SPIRIT-Surrogate): extension checklist with explanation and elaboration 16/05/2017 CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials 14/05/2017 SPIRIT 2013 Statement: Defining standard protocol items for clinical trials 23/10/2016 Improving the reporting quality of nonrandomized evaluations of behavioral and public health interventions: the TREND statement 20/08/2013 Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration 14/08/2013 Proposed best practice for statisticians in the reporting and publication of pharmaceutical industry-sponsored clinical trials 14/08/2013 Electrodermal activity at acupoints: literature review and recommendations for reporting clinical trials 13/08/2013 ASAS recommendations for collecting, analysing and reporting NSAID intake in clinical trials/epidemiological studies in axial spondyloarthritis 12/08/2013 American Society of Transplantation recommendations for screening, monitoring and reporting of infectious complications in immunosuppression trials in recipients of organ transplantation

Blog archives

Latest guest blogger

New resource for research teams to improve the reporting of implementation studies

In this blog post, Dr Louise Hull, an implementation research lead, discusses the development of a new resource to help improve the reporting of implementation studies.