Publications by authors named "Shanell Williams"

Background: The California Preterm Birth Initiative is a community-engaged research effort focused on addressing racial disparities in birth outcomes.

Objectives: To highlight three community-academic partnership strategies and identify partners' lessons learned and recommendations.

Methods: We conducted interviews (n = 38), four focus groups (n = 23), a document review (n = 174), and meeting/event observations (n = 36).

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Introduction: Mistreatment by health care providers disproportionately affects Black, Indigenous, and other people of color in the United States. The goal of this study is to adapt the global Person-Centered Maternity Care (PCMC) scale for use in the United States, with particular attention to the experiences of Black women and birthing people.

Methods: We used a community-engaged approach including expert reviews and cognitive interviews to assess content validity, relevance, comprehension, and comprehensiveness of the PCMC items.

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Article Synopsis
  • - There are significant disparities in maternal mortality and birth outcomes among Black, Indigenous, and other people of color, highlighting the need for improved understanding of prenatal care experiences in these communities.
  • - The study aimed to create and validate a tool that measures person-centered prenatal care specifically tailored to the experiences of people of color in the U.S., employing community-based methods to ensure relevance and accuracy.
  • - After gathering data from 293 respondents, the researchers developed a 34-item scale and a stricter 26-item version to assess prenatal care quality, focusing on key areas like "dignity and respect" and "communication."
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This project examines risk and protective factors for preterm birth (PTB) among Black women in Oakland, California. Women with singleton births in 2011-2017 (n = 6199) were included. Risk and protective factors for PTB and independent risk groups were identified using logistic regression and recursive partitioning.

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Background: Traditional hierarchical approaches to research give privilege to small groups with decision-making power, without direct input from those with lived experience of illness who bear the burden of disease. A Research Justice framework values the expertise of patients and communities as well as their power in creating knowledge and in decisions about what research is conducted. Preterm birth has persisted at epidemic levels in the United States for decades and disproportionately affects women of color, especially Black women.

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Background: Chronic stress is a known risk factor for preterm birth, yet little is known about how healthcare experiences add to or mitigate perceived stress. In this study, we described the pregnancy-related healthcare experiences of 54 women of color from Fresno, Oakland, and San Francisco, California, with social and/or medical risk factors for preterm birth.

Methods: This study was a secondary analysis of focus group data generated as part of a larger project focused on patient and community involvement in preterm birth research.

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Involvement of patients and the public is now recognized to be essential for the good conduct of research. Patient and public involvement in research priority setting and funding decisions is only beginning to be recognized as important, and methods for doing so are nascent. This protocol describes the Research Prioritization by Affected Communities (RPAC) protocol and findings from its use with women at high socio-demographic risk for preterm birth.

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