Literature DB >> 28596181

Evolution of poor reporting and inadequate methods over time in 20 920 randomised controlled trials included in Cochrane reviews: research on research study.

Agnes Dechartres1,2,3,4, Ludovic Trinquart1,2, Ignacio Atal1,2, David Moher5, Kay Dickersin6, Isabelle Boutron1,2,3,4, Elodie Perrodeau1,3, Douglas G Altman7, Philippe Ravaud1,2,3,8,4.   

Abstract

Objective To examine how poor reporting and inadequate methods for key methodological features in randomised controlled trials (RCTs) have changed over the past three decades.Design Mapping of trials included in Cochrane reviews.Data sources Data from RCTs included in all Cochrane reviews published between March 2011 and September 2014 reporting an evaluation of the Cochrane risk of bias items: sequence generation, allocation concealment, blinding, and incomplete outcome data.Data extraction For each RCT, we extracted consensus on risk of bias made by the review authors and identified the primary reference to extract publication year and journal. We matched journal names with Journal Citation Reports to get 2014 impact factors.Main outcomes measures We considered the proportions of trials rated by review authors at unclear and high risk of bias as surrogates for poor reporting and inadequate methods, respectively.Results We analysed 20 920 RCTs (from 2001 reviews) published in 3136 journals. The proportion of trials with unclear risk of bias was 48.7% for sequence generation and 57.5% for allocation concealment; the proportion of those with high risk of bias was 4.0% and 7.2%, respectively. For blinding and incomplete outcome data, 30.6% and 24.7% of trials were at unclear risk and 33.1% and 17.1% were at high risk, respectively. Higher journal impact factor was associated with a lower proportion of trials at unclear or high risk of bias. The proportion of trials at unclear risk of bias decreased over time, especially for sequence generation, which fell from 69.1% in 1986-1990 to 31.2% in 2011-14 and for allocation concealment (70.1% to 44.6%). After excluding trials at unclear risk of bias, use of inadequate methods also decreased over time: from 14.8% to 4.6% for sequence generation and from 32.7% to 11.6% for allocation concealment.Conclusions Poor reporting and inadequate methods have decreased over time, especially for sequence generation and allocation concealment. But more could be done, especially in lower impact factor journals. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

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Year:  2017        PMID: 28596181     DOI: 10.1136/bmj.j2490

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


  37 in total

Review 1.  Enhancing primary reports of randomized controlled trials: Three most common challenges and suggested solutions.

Authors:  Guowei Li; Meha Bhatt; Mei Wang; Lawrence Mbuagbaw; Zainab Samaan; Lehana Thabane
Journal:  Proc Natl Acad Sci U S A       Date:  2018-03-12       Impact factor: 11.205

Review 2.  Standards for design and measurement would make clinical research reproducible and usable.

Authors:  Kay Dickersin; Evan Mayo-Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  2018-03-13       Impact factor: 11.205

3.  Do thermal treatments affect the mechanical behavior of porcelain-veneered zirconia? A systematic review and meta-analysis.

Authors:  Camila da Silva Rodrigues; Iana Lamadrid Aurélio; Marina da Rosa Kaizer; Yu Zhang; Liliana Gressler May
Journal:  Dent Mater       Date:  2019-03-04       Impact factor: 5.304

4.  Reporting Sample Size Calculation in Randomized Clinical Trials Published in 4 Orthodontic Journals.

Authors:  Marialicia Calderon-Augusto; Carlos Flores-Mir; Luis Ernesto Arriola-Guillén
Journal:  Turk J Orthod       Date:  2021-12

5.  Randomized clinical trials in dentistry: Risks of bias, risks of random errors, reporting quality, and methodologic quality over the years 1955-2013.

Authors:  Humam Saltaji; Susan Armijo-Olivo; Greta G Cummings; Maryam Amin; Carlos Flores-Mir
Journal:  PLoS One       Date:  2017-12-22       Impact factor: 3.240

6.  Simple decision-tree tool to facilitate author identification of reporting guidelines during submission: a before-after study.

Authors:  Daniel R Shanahan; Ines Lopes de Sousa; Diana M Marshall
Journal:  Res Integr Peer Rev       Date:  2017-12-18

7.  Description of complex interventions: analysis of changes in reporting in randomised trials since 2002.

Authors:  Bridget Candy; Victoria Vickerstaff; Louise Jones; Michael King
Journal:  Trials       Date:  2018-02-22       Impact factor: 2.279

8.  Quality of reporting for randomised clinical trials published in Latin American and Spanish journals: A protocol for a systematic survey of three clinical specialities.

Authors:  Vivienne C Bachelet; Víctor A Carrasco; Fabiana Bravo-Córdova; Ruben A Díaz; Francisca J Lizana; Nicolás Meza-Ducaud; Hector Pardo-Hernandez; Francisco A Uribe; Alonso F Vergara; Julio Villanueva; María S Navarrete
Journal:  BMJ Open       Date:  2020-06-21       Impact factor: 2.692

Review 9.  Outcome reporting recommendations for clinical trial protocols and reports: a scoping review.

Authors:  Nancy J Butcher; Emma J Mew; Andrea Monsour; An-Wen Chan; David Moher; Martin Offringa
Journal:  Trials       Date:  2020-07-08       Impact factor: 2.279

10.  Clinical trial registration and reporting: a survey of academic organizations in the United States.

Authors:  Evan Mayo-Wilson; James Heyward; Anthony Keyes; Jesse Reynolds; Sarah White; Nidhi Atri; G Caleb Alexander; Audrey Omar; Daniel E Ford
Journal:  BMC Med       Date:  2018-05-02       Impact factor: 8.775

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