Multilevel challenges to equitable inclusion of children in trials when parents use languages other than English: A qualitative report from Children's Oncology Group's Diversity and Health Disparities Committee Language Equity Working Group

Author:

Santacroce Sheila Judge1,Beauchemin Melissa P.2ORCID,Pelletier Wendy3,Robles Joanna M.4,Ruiz Jenny5ORCID,Blazin Lindsay J.67,Aristizabal Paula8ORCID,Orjuela‐Grimm Manuela9ORCID,Hall Anurekha G.10ORCID,Kahn Justine9ORCID,Kline Cassie11,Seif Alix E.11,Velez Maria C.12,Winestone Lena E.13ORCID

Affiliation:

1. University of North Carolina at Chapel Hill School of Nursing Chapel Hill North Carolina USA

2. Columbia University Mailman School of Nursing New York New York USA

3. University of Calgary Calgary Alberta Canada

4. Wake Forest University School of Medicine Winston‐Salem North Carolina USA

5. University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

6. Indiana University School of Medicine Indianapolis Indiana USA

7. Riley Children's Health Indianapolis Indiana USA

8. University of California San Diego Moores Cancer Center/University of California San Diego Department of Pediatrics Rady Children's Hospital San Diego San Diego California USA

9. New York Presbyterian/Columbia University Medical Center New York New York USA

10. University of Washington Seattle Children's Hospital Seattle Washington USA

11. Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

12. Children's Hospital New Orleans/Louisiana State University Health Sciences Center New Orleans Louisiana USA

13. Division of Allergy, Immunology & BMT University of California San Francisco Benioff Children's Hospitals San Francisco California USA

Abstract

AbstractBackgroundIncreasing representation in clinical trials is a priority for the National Cancer Institute and Children's Oncology Group (COG). Our survey of COG‐affiliated institutions revealed that many sites have insufficient processes and resources to enroll children whose parents use languages other than English (LOE). We describe reported barriers and facilitators to enrolling children in clinical trials when parents use LOE and propose opportunities for improvement.ProceduresWe sent a 20‐item survey to COG‐affiliated institutions. Five items allowed respondents to expand on replies to questions about (a) local institutional review board (IRB) requirements regarding translation of consent documents, (b) contributors to provider discomfort consenting parents who use LOE, (c) available language services and resources, and (d) barriers to enrolling children whose parents use LOE or offer ideas about approaches to improvements. Two pairs of researchers independently coded free‐text responses and compared results for concordance.ResultsA total of 139 (N = 230; 60%) institutions returned the survey. Respondents were mainly physician principal investigators (n = 79/139; 57%) at the United States sites (n = 118/139; 85%) serving less than 100 newly diagnosed children per year (n = 99/139, 71%). They described challenges at multiple levels. Proposed approaches to improvements included centralized provision of translated materials and video educational materials in various languages, and collaborating with IRBs on regulatory processes that protect families and facilitate equitable clinical trial access.ConclusionsClinical trial consortia, such as COG, face challenges in enrolling representative samples. Further research is required to design and implement multilevel interventions to ensure equitable access for all, regardless of language used, and mitigate disparate research participation.

Funder

Leukemia and Lymphoma Society

Publisher

Wiley

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