School of Public Health, University of California, 2121 Berkeley Way #5302, Berkeley, CA, 94720, USA.
Sexual Health and Reproductive Equity Program, School of Social Welfare, University of California, 120 Haviland Hall, Berkeley, CA, 94720-7400, USA.
Matern Child Health J. 2024 Mar;28(3):400-408. doi: 10.1007/s10995-023-03883-2. Epub 2024 Jan 24.
In an effort to address persistent inequities in maternal and infant health, policymakers and advocates have pushed to expand access to doula care. Several states, including California, now cover doula services through Medicaid. As coverage expands, research on the impact of doula care will likely increase. To develop best practices for research, it is critical to engage community doulas, clients, and other key stakeholders.
Our overarching goal was to build capacity for future doula- and client-centered research on community doula care. First, we established a Steering Committee with members from seven relevant stakeholder groups: community doulas, former or potential doula clients, clinicians, payers, advocates, researchers, and public health professionals. Second, we conducted a needs assessment to identify and understand stakeholders' needs and values for research on community doula care. Findings from the needs assessment informed our third step, conducting a research prioritization to develop a shared research agenda related to community doula care with the Steering Committee. We adapted the Research Prioritization by Affected Communities protocol to guide this process, which resulted in a final list of 21 priority research questions. Lastly, we offered a training to increase capacity among community doulas to engage in research on community doula care.
Our findings provide direction for those interested in conducting research on doula care, as well as policymakers and funders.
The findings of our stakeholder-engaged process provide a roadmap that will lead to equity-oriented research centering clients, doulas, and their communities.
为了解决母婴健康方面持续存在的不平等问题,政策制定者和倡导者一直在努力扩大导乐服务的可及性。包括加利福尼亚州在内的几个州现在通过医疗补助计划覆盖导乐服务。随着覆盖面的扩大,关于导乐护理影响的研究可能会增加。为了制定研究的最佳实践,与社区导乐、客户和其他利益相关者合作至关重要。
我们的总体目标是为未来以社区导乐和客户为中心的社区导乐护理研究建立能力。首先,我们成立了一个指导委员会,成员来自七个相关利益相关者群体:社区导乐、前或潜在的导乐客户、临床医生、付款人、倡导者、研究人员和公共卫生专业人员。其次,我们进行了需求评估,以确定和了解利益相关者对社区导乐护理研究的需求和价值观。需求评估的结果为我们的第三步提供了信息,即与指导委员会一起进行研究优先级排序,制定与社区导乐护理相关的共同研究议程。我们采用受影响社区的研究优先排序协议来指导这一过程,最终确定了 21 个优先研究问题的最终清单。最后,我们提供了培训,以提高社区导乐参与社区导乐护理研究的能力。
我们的研究结果为那些对导乐护理研究感兴趣的人以及政策制定者和资助者提供了指导。
我们的利益相关者参与过程的结果提供了一个路线图,将导致以客户、导乐和他们的社区为中心的公平导向研究。