SAFETYLIT WEEKLY UPDATE

We compile citations and summaries of about 400 new articles every week.
RSS Feed

HELP: Tutorials | FAQ
CONTACT US: Contact info

Search Results

Journal Article

Citation

Otte WM, Tijdink JK, Weerheim PL, Lamberink HJ, Vinkers CH. Elife 2018; 7: e34412.

Affiliation

Department of Psychiatry, Brain Centre Rudolf Magnus, University Medical Center Utrecht/Utrecht University, Utrecht, The Netherlands.

Copyright

(Copyright © 2018, dLife Sciences Plublications, Ltd)

DOI

10.7554/eLife.34412

PMID

29866256

PMCID

PMC5988419

Abstract

Clinical trials have a vital role in ensuring the safety and efficacy of new treatments and interventions in medicine. A key characteristic of a clinical trial is its statistical power. Here we investigate whether the statistical power of a trial is related to the gender of first and last authors on the paper reporting the results of the trial. Based on an analysis of 31,873 clinical trials published between 1974 and 2017, we find that adequate statistical power was most often present in clinical trials with a male first author and a female last author (20.6%, 95% confidence interval 19.4-21.8%), and that this figure was significantly higher than the percentage for other gender combinations (12.5-13.5%; P<0.0001). The absolute number of female authors in clinical trials gradually increased over time, with the percentage of female last authors rising from 20.7% (1975-85) to 28.5% (after 2005). Our results demonstrate the importance of gender diversity in research collaborations and emphasize the need to increase the number of women in senior positions in medicine.

© 2018, Otte et al.


Language: en

Keywords

Cochrane meta-analysis; clinical study; human; human biology; medicine; meta research; mixed sex collaborations; randomized controlled trial (RCT); statistical power

NEW SEARCH


All SafetyLit records are available for automatic download to Zotero & Mendeley
Print