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A Multilevel Approach to Stakeholder Engagement in the Formulation of a Clinical Data Research Network.
Boyer, Alaina P; Fair, Alecia M; Joosten, Yvonne A; Dolor, Rowena J; Williams, Neely A; Sherden, Lisa; Stallings, Sarah; Smoot, Duane T; Wilkins, Consuelo H.
Afiliación
  • Boyer AP; Meharry-Vanderbilt Alliance.
  • Fair AM; Vanderbilt University School of Medicine, Nashville, TN.
  • Joosten YA; Vanderbilt University School of Medicine, Nashville, TN.
  • Dolor RJ; Duke University Medical Center, Durham, NC.
  • Williams NA; Community Partners Network.
  • Sherden L; Meharry-Vanderbilt Alliance.
  • Stallings S; Meharry-Vanderbilt Alliance.
  • Smoot DT; Meharry Medical College, Nashville, TN.
  • Wilkins CH; Meharry-Vanderbilt Alliance.
Med Care ; 56 Suppl 10 Suppl 1: S22-S26, 2018 10.
Article en En | MEDLINE | ID: mdl-30074947
OBJECTIVES: To ensure meaningful engagement of stakeholders (patients, clinicians, and communities) in developing the Mid-South Clinical Data Research Network (MS-CDRN), we implemented a comprehensive, multilevel approach: (1) identify barriers to involving stakeholders in governance, network design, and implementation; (2) engage stakeholders in priority setting and research topic generation; (3) develop strategies to fully integrate stakeholders in CDRN governance and oversight; and (4) solicit guidance on patient-centered tools and strategies for recruiting research participants. METHODS: We engaged stakeholders: (1) as integral research team members; (2) on oversight and advisory committees; (3) as consultants (using Community Engagement Studios); and (4) through interviews and surveys. We recruited stakeholders from community health centers, churches, barbershops, health fairs, a volunteer registry, and a patient portal. We prioritized recruitment from populations often underrepresented in research. RESULTS: During the first 18 months, we engaged 5670 stakeholders in developing the MS-CDRN. These were research team members and on governance committees (N=10), consultants (N=58), survey respondents (N=5543), and interviewees (N=59). Stakeholders identified important barriers and facilitators to engagement, developed stakeholder-informed policies, provided feedback on priority topics and research questions, and developed an intake process for data requests and interventional studies that included reviewing for appropriate patient-centeredness, patient engagement, and dissemination. DISCUSSION: Multilevel stakeholder engagement is a novel systematic approach to developing a meaningful patient-centered and patient-engaged research program. This approach allows ongoing input from highly engaged stakeholders while leveraging focused input from larger, more diverse groups to enhance the patient-centeredness of research and increase relevance to broader audiences.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Participación del Paciente / Atención Dirigida al Paciente / Investigación sobre la Eficacia Comparativa / Evaluación del Resultado de la Atención al Paciente / Participación de los Interesados Tipo de estudio: Guideline / Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Med Care Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Participación del Paciente / Atención Dirigida al Paciente / Investigación sobre la Eficacia Comparativa / Evaluación del Resultado de la Atención al Paciente / Participación de los Interesados Tipo de estudio: Guideline / Prognostic_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Med Care Año: 2018 Tipo del documento: Article