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Community-Based Participatory Research (CBPR) to Enhance Participation of Racial/Ethnic Minorities in Clinical Trials: A 10-Year Systematic Review.
Julian McFarlane, Soroya; Occa, Aurora; Peng, Wei; Awonuga, Oluwatumininu; Morgan, Susan E.
Afiliación
  • Julian McFarlane S; Department of Communication Studies, University of Georgia.
  • Occa A; Department of Communication, University of Kentucky.
  • Peng W; Murrow College of Communication, Washington State University.
  • Awonuga O; Department of Communication Studies, University of Georgia.
  • Morgan SE; School of Communication, University of Miami.
Health Commun ; 37(9): 1075-1092, 2022 08.
Article en En | MEDLINE | ID: mdl-34420460
ABSTRACT
There has not been a significant improvement in the rate of clinical trial accrual in more than 20 years. Worse, the challenge of inadequate representation among racial and ethnic minorities also persists, deepening disparities in health. Community-Based Participatory Research (CBPR) is a participatory communication method that centers on effective dialogue between researchers and community stakeholders with the goal of creating an equitable partnership for health and social change. The objective of the current study was to provide an update since a systematic review in 2012, on the current status of the empirical research, with a particular focus on the elements of CBPR methods used to improve the rate of accrual of members of racial and ethnic minority communities for clinical trials. Our systematic review found a large increase in the number of CBPR related studies and studies related to racial and ethnic representation in research. More than 85% of studies employing CBPR methods saw statistically positive outcomes. Specifically, the elements of CBPR that are associated with these positive outcomes include community partner participation in (1) a study advisory committee, (2) data collection, (3) the development of interventions, and (4) participant recruitment. However, the results of our study indicate that researchers need to be more transparent about the extent of community participation as well as more thoroughly and accurately describe the nature of the partnership with members of minority communities in order to build upon the scientific literature on community-engaged methods.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Participación del Paciente / Ensayos Clínicos como Asunto / Minorías Étnicas y Raciales Tipo de estudio: Systematic_reviews Límite: Humans Idioma: En Revista: Health Commun Asunto de la revista: PESQUISA EM SERVICOS DE SAUDE / SERVICOS DE SAUDE Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Participación del Paciente / Ensayos Clínicos como Asunto / Minorías Étnicas y Raciales Tipo de estudio: Systematic_reviews Límite: Humans Idioma: En Revista: Health Commun Asunto de la revista: PESQUISA EM SERVICOS DE SAUDE / SERVICOS DE SAUDE Año: 2022 Tipo del documento: Article