Julian Bowen Consort Dining Table, Honey, Height: 77, Width: 92, Depth: 92cm

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Authors should address generalisability, or the extent to which the authors believe that trial results can be expected in other situations [ 66]. For cluster randomised trials, authors should follow the CONSORT Extension to Cluster Randomised Trials. The abstract needs to be well written, since readers tend to assess the overall quality of the trial just by reading the abstract.

CONSORT 2010 statement: extension checklist for reporting

Console tables are sleek and narrow, so you can enjoy incredible aesthetics and functionality without sacrificing space. The results of RCTs are of optimal use when authors report their methods and results accurately, completely, and transparently. STRICTA Controlled trials of acupuncture: MacPherson H, Altman DG, Hammerschlag R, Youping L, Taixiang W, White A, Moher D; STRICTA Revision Group. CONSORT-DEFINE: Yap C, Solovyeva O, de Bono J, Rekowski J, Patel D, Jaki T, Mander A, Evans TRJ, Peck R, Hayward KS, Hopewell S, Ursino M, Rantell KR, Calvert M, Lee S, Kightley A, Ashby D, Chan AW, Garrett-Mayer E, Isaacs JD, Golub R, Kholmanskikh O, Richards D, Boix O, Matcham J, Seymour L, Ivy SP, Marshall LV, Hommais A, Liu R, Tanaka Y, Berlin J, Espinasse A, Dimairo M, Weir CJ. Constructed from solid Malaysian Hardwood in a honey pine lacquer finish allows this table to match almost anything, or simply match with the Consort dining chairs!The Discussion section should include supporting evidence to the trial's findings along with the pros and cons of the results obtained. We developed an extension of the CONSORT 2010 Statement for Social and Psychological Interventions (CONSORT-SPI 2018) [ 34]. CONSORT-SPI 2018, like all CONSORT guidance, is an evolving document with a continuous and iterative process of assessment and refinement over time. Authors may wish to discuss plausible alternative explanations for results other than differences in effects between interventions [ 44].

CONSORT 2010 statement: extension to randomised crossover

Since the revision in 2001, the evidence base to inform CONSORT has grown considerably; empirical data highlighting new concerns regarding the reporting of randomized trials. CONSORT for pilot and feasibility trials: Eldridge SM, Chan CL, Campbell MJ, Bond CM, Hopewell S, Thabane L, Lancaster GA; on behalf of the PAFS consensus group. Clinical trial registration: a statement from the International Committee of Medical Journal Editors. As part of the growing open-science movement, triallists are increasingly expected to maintain their datasets, linked via trial registrations and posted in trusted online repositories (see http://www. which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.Reporting randomised trials of social and psychological interventions: the CONSORT-SPI 2018 Extension. Authors should pay particular attention to topic-specific information related to socioeconomic and other inequalities [ 88, 89, 90]. The checklist items focus on reporting how the trial was designed, analyzed, and interpreted; the flow diagram displays the progress of all participants through the trial. In addition to the eligibility criteria that apply to individuals, social and psychological intervention trials often have eligibility criteria for the settings where participants will be recruited and interventions delivered, as well as intervention providers [ 44].