Creation of standardized tools to evaluate reporting in health research: Population Reporting Of Gender, Race, Ethnicity & Sex (PROGRES)

Author:

Stey Anne M.ORCID,Ghneim Mira,Gurney OnaonaORCID,Santos Ariel P.ORCID,Rattan Rishi,Abahuje EgideORCID,Baskaran ArchitORCID,Nahmias Jeffry,Richardson Joseph,Zakrison Tanya L.,Baily Zinzi D.,Haut Elliott R.ORCID,Chaudhary Mihir,Joseph Bellal,Zarzaur Ben,Hendershot Kimberly

Abstract

Despite increasing diversity in research recruitment, research finding reporting by gender, race, ethnicity, and sex has remained up to the discretion of authors. This study developped and piloted tools to standardize the inclusive reporting of gender, race, ethnicity, and sex in health research. A modified Delphi approach was used to develop standardized tools for the inclusive reporting of gender, race, ethnicity, and sex in health research. Health research, social epidemiology, sociology, and medical anthropology experts from 11 different universities participated in the Delphi process. The tools were pilot tested on 85 health research manuscripts in top health research journals to determine inter-rater reliability of the tools. The tools each spanned five dimensions for both sex and gender as well as race and ethnicity: Author inclusiveness, Participant inclusiveness, Nomenclature reporting, Descriptive reporting, and Outcomes reporting for each subpopulation. The sex and gender tool had a median score of 6 and a range of 1–15 out of 16 possible points. The percent agreement between reviewers piloting the sex and gender tool was 82%. The interrater reliability or average Cohen’s Kappa was 0.54 with a standard deviation of 0.33 demonstrating moderate agreement. The race and ethnicity tool had a median score of 1 and a range of 0–15 out of 16 possible points. Race and ethnicity were both reported in only 25.8% of studies evaluated. Most studies that reported race reported only the largest subgroups; White, Black, and Latinx. The percent agreement between reviewers piloting the race and ethnicity tool was 84 and average Cohen’s Kappa was 0.61 with a standard deviation of 0.38 demonstrating substantial agreement. While the overall dimension scores were low (indicating low inclusivity), the interrater reliability measures indicated moderate to substantial agreement for the respective tools. Efforts in recruitment alone will not provide more inclusive literature without improving reporting.

Publisher

Public Library of Science (PLoS)

Reference19 articles.

1. Approach to High Volume Enrollment in Clinical Research: Experiences from an All of Us Research Program Site.;TO Ilori;Clin Transl Sci,2020

2. Investigators’ assessment of NIH mandated inclusion of women and minorities in research.;GM Corbie-Smith;Contemp Clin Trials.,2006

3. How the new NIH Guidelines on Inclusion of Women and Minorities apply: efficacy trials, effectiveness trials, and validity;AA Hohmann;J Consult Clin Psychol,1996

4. Systematic review identified suboptimal reporting and use of race/ethnicity in general medical journals.;IW Ma;J Clin Epidemiol. 2007 Jun,2007

5. Report on EQUATOR Network launch meeting 26th June 2008 "Achieving Transparency in Reporting Health Research".;H. Thornton;Int J Surg.,2008

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3