Literature DB >> 33973413

Using Critical Race Theory to Understand Trial Participation Among Black Individuals With Systemic Lupus Erythematosus: A Qualitative Study of Patients and Caregivers.

Rodlescia S Sneed1, Maryann Mason2, Jessica N Williams3, Corine Sinnette3, Kreager Taber3, Karen Mancera-Cuevas4, Gina Curry5, Patricia Canessa6, Rosalind Ramsey-Goldman2, Candace H Feldman3.   

Abstract

OBJECTIVE: Black patients with systemic lupus erythematous (SLE) experience greater disease incidence and severity than White patients, and yet they are underrepresented in SLE clinical trials. We applied Critical Race Theory to qualitatively explore the influence of racism on the underrepresentation of Black patients in SLE clinical trials and to develop a framework for future intervention.
METHODS: We conducted focus group sessions in Chicago and Boston with Black adults (ages ≥18 years) with SLE and their caregivers. We queried the participants about their knowledge regarding clinical trials, factors that might motivate or hinder trial participation, and how race and experiences of racism might impact clinical trial participation. Focus group responses were transcribed verbatim and analyzed thematically.
RESULTS: We held 4 focus groups (n = 31 participants); 20 participants had SLE, and 11 were caregivers. All participants were Black, 90% were women, and the mean age was 54 years. Qualitative analyses revealed several themes that negatively impact trial participation, including mistrust related to racism, concerns about assignment to placebo groups, strict study exclusion criteria, and SLE-related concerns. Factors that motivated trial participation included recommendations from physicians and reputable institutions, a desire to help the greater good, and culturally sensitive marketing of trials.
CONCLUSION: Actions to improve clinical trial participation among Black individuals should focus on reframing how trial information is presented and disseminated and on reevaluating barriers that may restrict trial participation. Additionally, researchers must acknowledge and respond to the presence of racial bias in health care. Community-academic partnerships may help build trust and reduce fears of mistreatment among Black individuals with SLE.
© 2021, American College of Rheumatology.

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Year:  2021        PMID: 33973413      PMCID: PMC8557360          DOI: 10.1002/acr.24635

Source DB:  PubMed          Journal:  Arthritis Care Res (Hoboken)        ISSN: 2151-464X            Impact factor:   5.178


  23 in total

1.  The importance of race and ethnic background in biomedical research and clinical practice.

Authors:  Esteban González Burchard; Elad Ziv; Natasha Coyle; Scarlett Lin Gomez; Hua Tang; Andrew J Karter; Joanna L Mountain; Eliseo J Pérez-Stable; Dean Sheppard; Neil Risch
Journal:  N Engl J Med       Date:  2003-03-20       Impact factor: 91.245

2.  The public health critical race methodology: praxis for antiracism research.

Authors:  Chandra L Ford; Collins O Airhihenbuwa
Journal:  Soc Sci Med       Date:  2010-08-11       Impact factor: 4.634

3.  African Americans and Clinical Research: Evidence Concerning Barriers and Facilitators to Participation and Recruitment Recommendations.

Authors:  Travonia B Hughes; Vijay R Varma; Corinne Pettigrew; Marilyn S Albert
Journal:  Gerontologist       Date:  2017-04-01

Review 4.  Barriers to Clinical Research Participation Among African Americans.

Authors:  Rebecca Luebbert; Amelia Perez
Journal:  J Transcult Nurs       Date:  2015-03-09       Impact factor: 1.959

5.  Population-based incidence and prevalence of systemic lupus erythematosus: the Michigan Lupus Epidemiology and Surveillance program.

Authors:  Emily C Somers; Wendy Marder; Patricia Cagnoli; Emily E Lewis; Peter DeGuire; Caroline Gordon; Charles G Helmick; Lu Wang; Jeffrey J Wing; J Patricia Dhar; James Leisen; Diane Shaltis; W Joseph McCune
Journal:  Arthritis Rheumatol       Date:  2014-02       Impact factor: 10.995

6.  Factors Associated with Participation in Rheumatic Disease-Related Research among Underrepresented Populations: A Qualitative Systematic Review.

Authors:  Kaitlin Lima; Courtnie R Phillip; Jessica Williams; Jonna Peterson; Candace H Feldman; Rosalind Ramsey-Goldman
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-07-26       Impact factor: 4.794

7.  Implementation and dissemination of an African American popular opinion model to improve lupus awareness: an academic-community partnership.

Authors:  C R Phillip; K Mancera-Cuevas; C Leatherwood; J S Chmiel; D L Erickson; E Freeman; G Granville; M Dollear; K Walker; R McNeil; C Correia; P Canessa; R Ramsey-Goldman; C H Feldman
Journal:  Lupus       Date:  2019-10-08       Impact factor: 2.911

Review 8.  The Representation of Gender and Race/Ethnic Groups in Randomized Clinical Trials of Individuals with Systemic Lupus Erythematosus.

Authors:  Titilola Falasinnu; Yashaar Chaichian; Michelle B Bass; Julia F Simard
Journal:  Curr Rheumatol Rep       Date:  2018-03-17       Impact factor: 4.592

9.  Engaging African ancestry participants in SLE clinical trials.

Authors:  Aderike Anjorin; Peter Lipsky
Journal:  Lupus Sci Med       Date:  2018-12-11

10.  Lupus patient decisions about clinical trial participation: a qualitative evaluation of perceptions, facilitators and barriers.

Authors:  Cristina Arriens; Teresa Aberle; Fredonna Carthen; Stan Kamp; Aikaterini Thanou; Eliza Chakravarty; Judith A James; Joan T Merrill; Motolani E Ogunsanya
Journal:  Lupus Sci Med       Date:  2020-03-15
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