TRIALS 潤色咨詢

Trials

出版年份:2006 年文章數:6438 投稿命中率: 開通期刊會員,數據隨心看

出版周期:Irregular 自引率:9.1% 審稿周期: 開通期刊會員,數據隨心看

前往期刊查詢

投稿信息

投稿信息
審稿費用
暫無數據
版面費用
15330.0元/篇 (網友貢獻,非官方數據)
中國人發(fā)表比例
2023年中國人文章占該期刊總數量暫無數據 (2022年為100.00%)
自引率
9.1 %
年文章數
6438
期刊官網
點擊查看 (點擊次數:11211)
投稿鏈接
點擊查看 (點擊次數:4781次)
作者需知
點擊查看 (點擊次數:1164次)
期刊簡介
稿件收錄要求
Published by BioMed Central. ISSN: 1745-6215.

Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported. The impact factor shown relates to articles published in CCTCVM during 2003-4. Making all its content open access and not retaining copyright, Trials offers a way to make data both freely available and highly visible to trialists worldwide; this will benefit the impact of your publication among peers and society. The journal has unrestricted space and takes advantage of all the technical possibilities available for electronic publishing. To date, journals have focused on reporting the results of trials, with very little coverage of why and how they are conducted. Reports of trials have been restricted both by authors and editors - both parties often select only a subset of the outcomes measured, while the latter often impose word limits on the articles published making it difficult to communicate the lessons learnt from conducting the trial, let alone include adequate details of how the trial was conducted. The Internet offers both unlimited space and interactivity, and we are keen to harness these attributes. For instance, trialists will be able to provide the detail required to be a true scientific record and do more to make the article's message comprehensible to a variety of reader groups. They will also be able to communicate not only all outcome measures, as well as varying analyses and interpretations, but also in-depth descriptions of what they did and what they learnt. This sharing of direct experience is fundamental to improving the quality and conduct of trials worldwide.