Neely Williams
Datos Biográficos
| ID | 5543824 |
|---|---|
| NOMBRE | Neely Williams |
| NOMBRES | Neely |
| APELLIDO | Williams |
| FIRMA | WILLIAMS N |
| AFILIACIONES | Community Partners |
| ORCID | 0000-0001-8870-224X |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 4 |
| TOTAL DE CITAS | 0 |
| TOTAL COMO AUTOR | 4 |
| TOTAL COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2018 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2026 |
| ÍNDICE H | 0 |
Addressing a gap in community-engaged research
Background: Community-engaged research depends on sharing findings effectively; however, few tools translate implementation capacity and readiness data into actionable feedback. This gap limits community organizations' ability to use results to guide health program implementation, build trust in research, and sustain ongoing participation. This study developed and used a tailored survey response report process for congregations participating in t…
Patient Voices Leading Change
As the 8 patient partners serving on the PCORnet ® Steering Committee, we stand at the forefront of a transformative movement in clinical research. PCORnet ® Network Partners have been pioneers in integrating patient voices into every aspect of the research process, and we applaud the progress in operationalizing the Patient-Centered Outcomes Research Institute’s (PCORI) Framework for Patient Engagement and for leading the way as funders to chang…
Community Experiences and Perceptions of Clinical and Translational Research and Researchers
Engaging communities in research is increasingly recognized as critical to translation of research into improved health outcomes. Our objective was to understand community stakeholders' perspectives on researchers, academic institutions, and how community is valued in research. A 45-item survey assessing experiences and perceptions of research (trust, community value, equity, researcher preparedness, indicators of successful engagement) was distr…
A Multilevel Approach to Stakeholder Engagement in the Formulation of a Clinical Data Research Network
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 stakeholder…
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Community Experiences and Perceptions of Clinical and Translational Research and Researchers
Engaging communities in research is increasingly recognized as critical to translation of research into improved health outcomes. Our objective was to understand community stakeholders' perspectives on researchers, academic institutions, and how community is valued in research. A 45-item survey assessing experiences and perceptions of research (trust, community value, equity, researcher preparedness, indicators of successful engagement) was distr…
A Multilevel Approach to Stakeholder Engagement in the Formulation of a Clinical Data Research Network
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 stakeholder…
Addressing a gap in community-engaged research
Background: Community-engaged research depends on sharing findings effectively; however, few tools translate implementation capacity and readiness data into actionable feedback. This gap limits community organizations' ability to use results to guide health program implementation, build trust in research, and sustain ongoing participation. This study developed and used a tailored survey response report process for congregations participating in t…
Patient Voices Leading Change
As the 8 patient partners serving on the PCORnet ® Steering Committee, we stand at the forefront of a transformative movement in clinical research. PCORnet ® Network Partners have been pioneers in integrating patient voices into every aspect of the research process, and we applaud the progress in operationalizing the Patient-Centered Outcomes Research Institute’s (PCORI) Framework for Patient Engagement and for leading the way as funders to chang…
Community engagement (3 obras) · Health Policy Implementation Science (3 obras) · Health care (2 obras) · Medical education (2 obras) · Medicine (2 obras) · Mental Health and Patient Involvement (2 obras) · Political science (2 obras) · Psychology (2 obras) · Public relations (2 obras) · Business (1 obras)