Demographic recruitment bias of adults in United States randomized clinical trials by disease categories between 2008 to 2019: a systematic review and meta-analysis

被引:18
|
作者
Buffenstein, Ilana [1 ]
Kaneakua, Bree [1 ]
Taylor, Emily [1 ]
Matsunaga, Masako [1 ,2 ]
Choi, So Yung [1 ,2 ]
Carrazana, Enrique [1 ,3 ]
Viereck, Jason [1 ,3 ]
Liow, Kore Kai [1 ,3 ]
Ghaffari-Rafi, Arash [1 ,4 ]
机构
[1] Univ Hawaii Manoa, John A Burns Sch Med, 651 Ilalo St, Honolulu, HI 96813 USA
[2] Univ Hawaii Manoa, John A Burns Sch Med, Dept Quantitat Hlth Sci, Biostat Core Facil, 651 Ilalo St, Honolulu, HI 96813 USA
[3] Hawaii Pacific Neurosci, Comprehens Epilepsy Ctr, Innovat & Translat Lab, 2230 Liliha St 104, Honolulu, HI 96817 USA
[4] Univ Calif, Sch Med, Dept Neurol Surg, 4301 10St, Sacramento, CA 95817 USA
关键词
NIH-REVITALIZATION-ACT; PATIENT INCOME LEVEL; MINORITY PARTICIPATION; GENDER-DIFFERENCES; TUSKEGEE SYPHILIS; SEX; HEALTH; RISK; DISPARITIES; PREVALENCE;
D O I
10.1038/s41598-022-23664-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To promote health equity within the United States (US), randomized clinical trials should strive for unbiased representation. Thus, there is impetus to identify demographic disparities overall and by disease category in US clinical trial recruitment, by trial phase, level of masking, and multi-center status, relative to national demographics. A systematic review and meta-analysis were conducted using MEDLINE, Embase, CENTRAL, and ClinicalTrials.gov, between 01/01/2008 to 12/30/2019. Clinical trials (N = 5,388) were identified based on the following inclusion criteria: study type, location, phase, and participant age. Each clinical trial was independently screened by two researchers. Data was pooled using a random-effects model. Median proportions for gender, race, and ethnicity of each trial were compared to the 2010 US Census proportions, matched by age. A second analysis was performed comparing gender, race, and ethnicity proportions by trial phase, multi-institutional status, quality, masking, and study start year. 2977 trials met inclusion criteria (participants, n = 607,181) for data extraction. 36% of trials reported ethnicity and 53% reported race. Three trials (0.10%) included transgender participants (n = 5). Compared with 2010 US Census data, females (48.3%, 95% CI 47.2-49.3, p < 0.0001), Hispanics (11.6%, 95% CI 10.8-12.4, p < 0.0001), American Indians and Alaskan Natives (AIAN, 0.19%, 95% CI 0.15-0.23, p < 0.0001), Asians (1.27%, 95% CI 1.13-1.42, p < 0.0001), Whites (77.6%, 95% CI 76.4-78.8, p < 0.0001), and multiracial participants (0.25%, 95% CI 0.21-0.31, p < 0.0001) were under-represented, while Native Hawaiians and Pacific Islanders (0.76%, 95% CI 0.71- 0.82, p < 0.0001) and Blacks (17.0%, 95% CI 15.9-18.1, p < 0.0001) were over-represented. Inequitable representation was mirrored in analysis by phase, institutional status, quality assessment, and level of masking. Between 2008 to 2019 representation improved for only females and Hispanics. Analysis stratified by 44 disease categories (i.e., psychiatric, obstetric, neurological, etc.) exhibited significant yet varied disparities, with Asians, AIAN, and multiracial individuals the most under-represented. These results demonstrate disparities in US randomized clinical trial recruitment between 2008 to 2019, with the reporting of demographic data and representation of most minorities not having improved over time.
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页数:17
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