Literature DB >> 35875251

Race/ethnicity reporting and representation in US clinical trials: a cohort study.

Brandon E Turner1,2, Jecca R Steinberg1, Brannon T Weeks1, Fatima Rodriguez3, Mark R Cullen4.   

Abstract

Background: Systemic progress in improving trial representation is uncertain, and previous analyses of minority trial participation have been limited to small cohorts with limited exploration of driving factors.
Methods: We analyzed detailed trial records from all US clinical trials registered in ClinicalTrials.gov from March 2000 to March 2020. Minority enrollment was compared to 2010 US Census demographic estimates using Wilcoxon test. We utilized logistic regression and generalized linear regression with a logit link to assess the association of possible drivers (including trials' funding source, size, phase, and design) with trials' disclosure of and amount of minority enrollment respectively. Findings: Among 20,692 US-based trials with reported results (representing ~4·76 million enrollees), only 43% (8,871/20,692) reported any race/ethnicity data. The majority of enrollees were White (median 79·7%; interquartile range [IQR] 61·9-90·0%), followed by Black (10·0%; IQR 2·5-23·5%), Hispanic/Latino (6·0%; IQR 0·43-15·4%), Asian (1·0%; IQR 0·0-4·1%), and American Indian (0·0%; IQR 0·0-0·2%). Median combined enrollment of minority race/ethnicity groups (Black, Hispanic/Latino, Asian, American Indian, Other/Multi) was below census estimates (27·6%) (p<0·001) however increased at an annual rate of 1·7%. Industry and Academic funding were negatively associated with race/ethnicity reporting (Industry adjusted odds ratio [aOR]: 0·42, 95% confidence interval [CI]: 0·38 to 0·46, p<0.0001; Academic aOR: 0·45, CI: 0·41 to 0·50, p<0.0001). Industry also had a negative association with the proportion of minority ethnicity enrollees (aOR: 0·69, CI: 0·60 to 0·79) compared to US Government-funded trials. Interpretation: Over the past two decades, the majority of US trials in ClinicalTrials.gov do not report race/ethnicity enrollment data, and minorities are underrepresented in trials with modest improvement over time. Funding: Stanford Medical Scholars Research Funding, the National Heart, Lung, and Blood Institute, NIH (1K01HL144607) and the American Heart Association/Robert Wood Johnson Medical Faculty Development Program.

Entities:  

Year:  2022        PMID: 35875251      PMCID: PMC9302767          DOI: 10.1016/j.lana.2022.100252

Source DB:  PubMed          Journal:  Lancet Reg Health Am        ISSN: 2667-193X


  20 in total

1.  The anatomy of medical research: US and international comparisons.

Authors:  Hamilton Moses; David H M Matheson; Sarah Cairns-Smith; Benjamin P George; Chase Palisch; E Ray Dorsey
Journal:  JAMA       Date:  2015-01-13       Impact factor: 56.272

Review 2.  Structural racism and health inequities in the USA: evidence and interventions.

Authors:  Zinzi D Bailey; Nancy Krieger; Madina Agénor; Jasmine Graves; Natalia Linos; Mary T Bassett
Journal:  Lancet       Date:  2017-04-08       Impact factor: 79.321

3.  Trial Reporting in ClinicalTrials.gov - The Final Rule.

Authors:  Deborah A Zarin; Tony Tse; Rebecca J Williams; Sarah Carr
Journal:  N Engl J Med       Date:  2016-09-16       Impact factor: 91.245

4.  Trustworthiness before Trust - Covid-19 Vaccine Trials and the Black Community.

Authors:  Rueben C Warren; Lachlan Forrow; David Augustin Hodge; Robert D Truog
Journal:  N Engl J Med       Date:  2020-10-16       Impact factor: 91.245

5.  Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study.

Authors:  Nicholas J DeVito; Seb Bacon; Ben Goldacre
Journal:  Lancet       Date:  2020-01-17       Impact factor: 79.321

6.  Gender, racial, and ethnic disclosure in NIH K-Award funded diabetes and obesity clinical trials.

Authors:  Carlos Guevara; Chad Cook; Natalie Herback; Ricardo Pietrobon; Danny O Jacobs; Thomas Parker Vail
Journal:  Account Res       Date:  2006 Oct-Dec       Impact factor: 2.622

7.  Racism is the public health crisis.

Authors:  Kehinde Andrews
Journal:  Lancet       Date:  2021-04-10       Impact factor: 79.321

Review 8.  Putting the data before the algorithm in big data addressing personalized healthcare.

Authors:  Eli M Cahan; Tina Hernandez-Boussard; Sonoo Thadaney-Israni; Daniel L Rubin
Journal:  NPJ Digit Med       Date:  2019-08-19

9.  Ten-Year Trends in Enrollment of Women and Minorities in Pivotal Trials Supporting Recent US Food and Drug Administration Approval of Novel Cardiometabolic Drugs.

Authors:  Muhammad Shahzeb Khan; Izza Shahid; Tariq Jamal Siddiqi; Safi U Khan; Haider J Warraich; Stephen J Greene; Javed Butler; Erin D Michos
Journal:  J Am Heart Assoc       Date:  2020-05-19       Impact factor: 5.501

10.  Assessment of the Inclusion of Racial/Ethnic Minority, Female, and Older Individuals in Vaccine Clinical Trials.

Authors:  Laura E Flores; Walter R Frontera; Michele P Andrasik; Carlos Del Rio; Antonio Mondríguez-González; Stephanie A Price; Elizabeth M Krantz; Steven A Pergam; Julie K Silver
Journal:  JAMA Netw Open       Date:  2021-02-01
View more
  2 in total

1.  Interventions to promote health equity: implications for implementation science in behavioral medicine.

Authors:  Kassandra I Alcaraz; Betina R Yanez
Journal:  Transl Behav Med       Date:  2022-10-07       Impact factor: 3.626

2.  Willingness to Participate in Health Research: Mexican and Mexican American Women's Perspectives.

Authors:  Yareli Cornejo-Torres; Emily Boniface; Edlyn Lopez; Katherin Gomez-Arboleda; Blair G Darney
Journal:  Womens Health Rep (New Rochelle)       Date:  2022-09-20
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.