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Increasing Clinical Trial Participation of Black Women Diagnosed with Breast Cancer

Datos Bibliográficos

ID2072964
AutoresRicki Fairley (Breast Cancer Alliance, autor de correspondencia), James W Lillard (Morehouse School of Medicine), Alexandra Berk (0000-0001-6243-0100, Invitae (United States)), Sophia Cornew (Invitae (United States)), Joseph Gaspero, James Gillespie (0000-0002-0355-4178), Latrisha L Horne (Morehouse School of Medicine), Sabrina Kidane, Sandra B Munro (0000-0002-9643-0528, Invitae (United States)), Matthew Parsons (0000-0002-2428-3215), Emily R Powers (0009-0009-9868-2516, Breast Cancer Alliance), Suzanne E Rizzo (GlaxoSmithKline (United States)), Alyson Tishcler, Hope Wohl (GlaxoSmithKline (United States)), Marisa C Wei, Marisa C Weiss (0000-0002-6955-4939, GlaxoSmithKline (United States))
Año2024
Volumen11
Número3
Páginas1701-1717
Fecha de publicación2024-06-01
Peer ReviewedSí
Open AccessSí
TipoARTICLE
RevistaJournal of Racial and Ethnic Health Disparities (JOURNAL)
Identificadores de la revistaISSN: 2196-8837 • E-ISSN: 2197-3792
EditorialSpringer Science and Business Media LLC (PUBLISHER)
DOI10.1007/s40615-023-01644-z
PMID37314691
OpenAlexW4380538551
IdiomaEN
Citas recibidas1
Referencias citadas41

Despite racial disparities in breast cancer mortality, Black women remain underrepresented in clinical trials. In this mixed methods research, 48 Black women were engaged via focus group discussions and in-depth interviews to better understand the lived experience of women with breast cancer. The results of this qualitative study informed the development of a subsequent online survey to identify barriers, motivators, and other factors that influence decision-making by Black women diagnosed with breast cancer when considering clinical trial participation. Among the 257 Black survey participants, most (95%) were aware of clinical trials; of those, most viewed them as lifesaving (81%) and/or benefiting others (90%). Negative perceptions such as serious side effects (58%), not receiving real treatment (52%), or risk of potential harm (62%) were indicated. Barriers included financial expenses (49%), concerns that their condition could be made worse (29%), that they would receive a placebo (28%), or that treatment was unapproved (28%). Participants were more likely than their health care providers (HCPs) to initiate discussions of clinical trials (53% versus 33%), and 29% of participants indicated a need for more information about risks and benefits, even after having those conversations. The most trustworthy sources of information on clinical trials were HCPs (66%) and breast cancer support groups (64%). These results suggest that trusted communities are key for providing education on clinical trials. However, there is also a need for HCPs to proactively discuss clinical trials with patients to ensure that they are adequately informed about all aspects of participation

Breast cancer · Cancer · Clinical trial · Family medicine · Pathology · Public health · Quality of Life Research · BRCA gene mutations in cancer · Ethics in Clinical Research · Global Cancer Incidence and Screening · Medicine · Epidemiology · Gerontology · Internal Medicine

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Obras citantes distintas1
Citas por año1
Intervalo de citas2025 - 2025 (1)
Velocidad de citaciónrecent
Altamente citadoNo
Tipos de citaNeutras: 1
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