Evidence map›Paper›PMID 29696236›Full record

ArticleContemporary clinical trials communications2018

Temporal trends and characteristics of clinical trials for which only one racial or ethnic group is eligible.

Brian L Egleston, Omar Pedraza, Yu-Ning Wong, Candace L Griffin, Eric A Ross, J Robert Beck

Abstract read
In one paragraph

Article in Contemporary clinical trials communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Cancer Health Literacy and Willingness to Participate in Cancer Research and Donate Bio-Specimens.International journal of environmental research and public health · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Brian L EglestonFox Chase Cancer Center, Temple University Health System, 333 Cottman Ave., Philadelphia, PA 19111, USA.
Omar PedrazaFox Chase Cancer Center, Temple University Health System, 333 Cottman Ave., Philadelphia, PA 19111, USA.
Yu-Ning WongFox Chase Cancer Center, Temple University Health System, 333 Cottman Ave., Philadelphia, PA 19111, USA.
Candace L GriffinJohns Hopkins University, Baltimore, MD, USA.
Eric A RossFox Chase Cancer Center, Temple University Health System, 333 Cottman Ave., Philadelphia, PA 19111, USA.
J Robert BeckFox Chase Cancer Center, Temple University Health System, 333 Cottman Ave., Philadelphia, PA 19111, USA.

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Eric Andrew Ross · 1985 to 2026
$138.8M
Clinical Trials with Exclusions Based on Race, Ethnicity, and English FluencyR03CA167264 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI EGLESTON, BRIAN L · 2013 to 2014
$176k
NCI NIH HHS P30 CA006927NCI NIH HHS R03 CA167264
6 · The paper itself

Abstract

backgroundIncreasing diversity in clinical trials may be worthwhile. We examined clinical trials that restricted eligibility to a single race or ethnicity.

methodsWe reviewed 19,246 trials registered on ClinicalTrials.gov through January 2013. We mapped trial ZIP-codes to U.S. Census and American Community Survey data. The outcome was whether trials required participants to be from a single racial or ethnic group.

resultsIn adjusted analyses, the odds of trials restricting eligibility to a single race/ethnicity increased by 4% per year (95% CI 1.01-1.08, p = .024). Behavioral (5.79% with single race/ethnicity requirements), skin-related (4.49%), and Vitamin D (6.14%) studies had higher rates of single race/ethnicity requirements. Many other trial-specific characteristics, such as funding agency and region of the U.S. in which the trial opened, were associated with eligibility restrictions. In terms of neighborhood characteristics, studies with single race eligibility requirements were more likely to be located in ZIP-codes with greater percentages of those self-reporting the characteristic. For example, 35.2% (SD = 24.9%) of the population self-reported themselves as Black or African American in ZIP-codes with trials requiring participants to be Black/African American, but only 5.9% (SD = 6.9%) self-reported themselves as Black/African American in ZIP-codes with trials that required Asian ethnicity. In ZIP-codes with trials requiring Asian ethnicity, 24.6% (SD = 16.2%) self-reported as Asian. In ZIP-codes with trials requiring Hispanic/Latino ethnicity, 33.3% (SD = 28.5%) self-reported as Hispanic/Latino. Neighborhood level poverty rates and reduced English language ability were also associated with more single race eligibility requirements.

conclusionsIn selected fields, there has been a modest temporal increase in single race/ethnicity inclusion requirements. Some studies may not fall under regulatory purview and hence may be less likely to include diverse samples. Conversely, some eligibility requirements may be related to health disparities research. Future work should examine whether targeted enrollment criteria facilitates development of personalized medicine or reduces trial access.

Indexed as

Clinical trialsEligibility requirementsNeighborhood characteristicsProtocols

Identifiers

PMID29696236
PMCPMC5898501

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.