Revised STandards for Reporting Interventions in Clinical Trials of Acupuncture (STRICTA): extending the CONSORT statement (Chinese version)

2010 ◽  
pp. 804-818 ◽  
Author(s):  
H MacPherson
2010 ◽  
Vol 16 (10) ◽  
pp. ST-1-ST-14 ◽  
Author(s):  
Hugh MacPherson ◽  
Douglas G. Altman ◽  
Richard Hammerschlag ◽  
Li Youping ◽  
Wu Taixiang ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Yi Yang ◽  
Lin-Peng Wang ◽  
Lei Zhang ◽  
Li-Chen Wang ◽  
Jia Wei ◽  
...  

De qiis a core concept of acupuncture and is necessary to produce therapeutic effect. In 2010,de qihas been received as a term in the official extension of the CONSORT Statement. However, there are few articles that discuss which factors have influences on obtainingde qiin clinical trials. This paper aims to explore these factors and give advice on trial design in order to optimizede qiin acupuncture RCTs.


2019 ◽  
Vol 43 (4) ◽  
pp. 219-230 ◽  
Author(s):  
Arturo Garrocho-Rangel ◽  
Socorro Ruiz-Rodríguez ◽  
César Gaitán-Fonseca ◽  
Amaury Pozos-Guillén

In order to include appropriate informed decisions on dental therapeutic or preventive procedures in children, Pediatric Dentists should apply the fundamentals of “Evidence-Based Dentistry” (EBD). This oral health approach assists clinicians in understanding and applying the most relevant research published on evidence in the clinical setting when treating their patients. One of the crucial steps of EBD is to critically appraise and use the primary articles about therapy or prevention, namely, Randomized Clinical Trials (RCT), the study design that best addresses the questions related with these clinical areas. The aim of the present paper was to provide the basic concepts and an example of how to critically read and understand articles on RCT studies in Pediatric Dentistry employing the CONSORT statement, a process that involves assessing the reliability of results, risk of bias (internal validity), and applicability of reported clinical findings (external validity).


2017 ◽  
Vol 31 (suppl 1) ◽  
Author(s):  
Alessandro Dourado LOGUERCIO ◽  
Bianca Medeiros MARAN ◽  
Taíse Alessandra HANZEN ◽  
Alexandra Mara de PAULA ◽  
Jorge PERDIGÃO ◽  
...  

PLoS Medicine ◽  
2010 ◽  
Vol 7 (6) ◽  
pp. e1000261 ◽  
Author(s):  
Hugh MacPherson ◽  
Douglas G. Altman ◽  
Richard Hammerschlag ◽  
Li Youping ◽  
Wu Taixiang ◽  
...  

2010 ◽  
Vol 3 (3) ◽  
pp. 140-155 ◽  
Author(s):  
Hugh MacPherson ◽  
Douglas G. Altman ◽  
Richard Hammerschlag ◽  
Li Youping ◽  
Wu Taixiang ◽  
...  

2017 ◽  
Vol 58 ◽  
pp. 54-59 ◽  
Author(s):  
Rafael Sarkis-Onofre ◽  
Victório Poletto-Neto ◽  
Maximiliano Sérgio Cenci ◽  
Tatiana Pereira-Cenci ◽  
David Moher

2009 ◽  
Vol 19 (9) ◽  
pp. 671
Author(s):  
A.M. O'Connor ◽  
J.M. Sargeant ◽  
I. Gardner ◽  
J. Dickson ◽  
M.E. Torrence

2010 ◽  
Vol 28 (2) ◽  
pp. 83-93 ◽  
Author(s):  
Hugh MacPherson ◽  
Douglas G Altman ◽  
Richard Hammerschlag ◽  
Youping Li ◽  
Taixiang Wu ◽  
...  

The STandards for Reporting Interventions in Clinical Trials of Acupuncture (STRICTA) were published in five journals in 2001 and 2002. These guidelines, in the form of a checklist and explanations for use by authors and journal editors, were designed to improve reporting of acupuncture trials, particularly the interventions, thereby facilitating their interpretation and replication. Subsequent reviews of the application and impact of STRICTA have highlighted the value of STRICTA as well as scope for improvements and revision. To manage the revision process a collaboration between the STRICTA Group, the CONSORT Group and the Chinese Cochrane Centre was developed in 2008. An expert panel with 47 participants was convened that provided electronic feedback on a revised draft of the checklist. At a subsequent face-to-face meeting in Freiburg, a group of 21 participants further revised the STRICTA checklist and planned dissemination. The new STRICTA checklist, which is an official extension of CONSORT, includes 6 items and 17 subitems. These set out reporting guidelines for the acupuncture rationale, the details of needling, the treatment regimen, other components of treatment, the practitioner background and the control or comparator interventions. In addition, and as part of this revision process, the explanations for each item have been elaborated, and examples of good reporting for each item are provided. In addition, the word ‘controlled’ in STRICTA is replaced by ‘clinical’, to indicate that STRICTA is applicable to a broad range of clinical evaluation designs, including uncontrolled outcome studies and case reports. It is intended that the revised STRICTA checklist, in conjunction with both the main CONSORT statement and extension for non-pharmacological treatment, will raise the quality of reporting of clinical trials of acupuncture.


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