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1.
Public Health Nurs ; 35(4): 353-359, 2018 07.
Article in English | MEDLINE | ID: mdl-29566271

ABSTRACT

OBJECTIVES: A community-academic team implemented a study involving collection of quantitative data using a computer-based audience response system (ARS) whereby community partners led data collection efforts. The team participated in a reflection exercise after the data collection to evaluate and identify best practices and lessons learned about the community partner-led process. DESIGN & SAMPLE: The methods involved a qualitative research consultant who facilitated the reflection exercise that consisted of two focus groups-one academic and one community research team members. The consultant then conducted content analysis. Nine members participated in the focus groups. RESULTS: The reflection identified the following themes: the positive aspects of the ARS; challenges to overcome; and recommendations for the future. CONCLUSION: The lessons learned here can help community-academic research partnerships identify the best circumstances in which to use ARS for data collection and practical steps to aid in its success.


Subject(s)
Community-Based Participatory Research/methods , Data Collection/methods , Focus Groups/methods , Community-Institutional Relations , Electronic Data Processing/methods , Exercise , Humans , Qualitative Research
2.
J Public Health (Oxf) ; 38(3): 502-510, 2016 09.
Article in English | MEDLINE | ID: mdl-26359314

ABSTRACT

BACKGROUND: Health assessments are used to prioritize community-level health concerns, but the role of individuals' health concerns and experiences is unknown. We sought to understand to what extent community health assessments reflect health concerns of the community-at-large versus a representation of the participants sampled. METHODS: We conducted a health assessment survey in 30 rural African American churches (n = 412). Multivariable logistic regression produced odds ratios examining associations between personal health concern (this health concern is important to me), personal health experience (I have been diagnosed with this health issue) and community health priorities (this health concern is important to the community) for 20 health issues. RESULTS: Respondents reported significant associations for 19/20 health conditions between personal health concern and the ranking of that concern as a community priority (all P < 0.05). Inconsistent associations were seen between personal health experience of a specific health condition and the ranking of that condition as a community priority. CONCLUSIONS: Personal health concerns reported by individuals in a study sample may impact prioritization of community health initiatives. Further research should examine how personal health concerns are formed.


Subject(s)
Health Knowledge, Attitudes, Practice , Public Health , Black or African American/psychology , Black or African American/statistics & numerical data , Community-Based Participatory Research , Female , Health Priorities/statistics & numerical data , Health Status , Health Surveys , Humans , Logistic Models , Male , Middle Aged , Rural Population/statistics & numerical data , Virginia
3.
Prev Chronic Dis ; 12: E115, 2015 Jul 23.
Article in English | MEDLINE | ID: mdl-26203813

ABSTRACT

BACKGROUND: Underrepresentation of racial minorities in research contributes to health inequities. Important factors contributing to low levels of research participation include limited access to health care and research opportunities, lack of perceived relevance, power differences, participant burden, and absence of trust. We describe an enhanced model of community engagement in which we developed a community-linked research infrastructure to involve minorities in research both as participants and as partners engaged in issue selection, study design, and implementation. COMMUNITY CONTEXT: We implemented this effort in Jefferson County, Arkansas, which has a predominantly black population, bears a disproportionate burden of chronic disease, and has death rates above state and national averages. METHODS: Building on existing community-academic partnerships, we engaged new partners and adapted a successful community health worker model to connect community residents to services and relevant research. We formed a community advisory board, a research collaborative, a health registry, and a resource directory. OUTCOME: Newly formed community-academic partnerships resulted in many joint grant submissions and new projects. Community health workers contacted 2,665 black and 913 white community residents from December 2011 through April 2013. Eighty-five percent of blacks and 88% of whites were willing to be re-contacted about research of potential interest. Implementation challenges were addressed by balancing the needs of science with community needs and priorities. INTERPRETATION: Our experience indicates investments in community-linked research infrastructure can be fruitful and should be considered by academic health centers when assessing institutional research infrastructure needs.


Subject(s)
Chronic Disease/prevention & control , Community Participation/trends , Community-Based Participatory Research , Healthcare Disparities , Minority Groups/psychology , Arkansas , Chronic Disease/epidemiology , Chronic Disease/mortality , Community Health Workers/education , Community-Institutional Relations , Cooperative Behavior , Health Plan Implementation , Health Services Needs and Demand , Health Status Indicators , Humans , Minority Groups/statistics & numerical data , Organizational Case Studies , Registries , Socioeconomic Factors
4.
Contemp Clin Trials ; 64: 22-29, 2018 01.
Article in English | MEDLINE | ID: mdl-29170075

ABSTRACT

Rural African Americans are disproportionately exposed to numerous stressors such as poverty that place them at risk for experiencing elevated levels of depressive symptoms. Effective treatments for decreasing depressive symptoms exist, but rural African Americans often fail to receive adequate and timely care. Churches have been used to address physical health outcomes in rural African American communities, but few have focused primarily on addressing mental health outcomes. Our partnership, consisting of faith community leaders and academic researchers, adapted an evidence-based behavioral activation intervention for use with rural African American churches. This 8-session intervention was adapted to include faith-based themes, Scripture, and other aspects of the rural African American faith culture (e.g. bible studies) This manuscript describes a Hybrid-II implementation trial that seeks to test the effectiveness of the culturally adapted evidence-based intervention (Renewed and Empowered for the Journey to Overcome in Christ: REJOICE) and gather preliminary data on the strategies necessary to support the successful implementation of this intervention in 24 rural African American churches. This study employs a randomized one-way crossover cluster design to assess effectiveness in reducing depressive symptoms and gather preliminary data regarding implementation outcomes, specifically fidelity, associated with 2 implementation strategies: training only and training+coaching calls. This project has the potential to generate knowledge that will lead to improvements in the provision of mental health interventions within the rural African American community. Further, the use of the Hybrid-II design has the potential to advance our understanding of strategies that will support the implementation of and sustainability of mental health interventions within rural African American faith communities. TRIAL REGISTRATION: NCT02860741. Registered August 5, 2016.


Subject(s)
Behavior Therapy/methods , Black or African American , Depression/therapy , Faith-Based Organizations/organization & administration , Health Promotion/organization & administration , Rural Population , Community Health Services/organization & administration , Cross-Over Studies , Cultural Competency , Depression/ethnology , Female , Humans , Male , Research Design , Southeastern United States
5.
Prog Community Health Partnersh ; 11(1): 81-86, 2017.
Article in English | MEDLINE | ID: mdl-28603154

ABSTRACT

BACKGROUND: Academic partners typically build community capacity for research, but few examples exist whereby community partners build community research capacity. This paper describes the benefits of communities sharing their "best practices" with each other for the purpose of building health research capacity. METHODS: In the context of a grant designed to engage African American communities to address health disparities (Faith Academic Initiatives Transforming Health [FAITH] in the Delta), leaders of two counties exchanged their "best practices" of creating faith-based networks and community health assessment tools to conduct a collective health assessment. LESSONS LEARNED: There were numerous strengths in engaging communities to build each other's capacity to conduct research. Communities identified with each other, perceived genuineness, conveyed legitimacy, and provided insider knowledge. CONCLUSIONS: Engaging communities to build each other's research capacity is a potentially valuable strategy.


Subject(s)
Black or African American , Capacity Building/organization & administration , Community Networks/organization & administration , Community-Based Participatory Research , Community-Institutional Relations , Health Promotion/organization & administration , Arkansas , Health Status Disparities , Humans , Rural Population
6.
Article in English | MEDLINE | ID: mdl-24859098

ABSTRACT

BACKGROUND: The Mental Health-Clergy Partnership Program established partnerships between institutional (Department of Veterans' Affairs [VA] chaplains, mental health providers) and community (local clergy, parishioners) groups to develop programs to assist rural veterans with mental health needs. OBJECTIVES: Describe the development, challenges, and lessons learned from the Mental Health-Clergy Partnership Program in three Arkansas towns between 2009 and 2012. METHODS: Researchers identified three rural Arkansas sites, established local advisory boards, and obtained quantitative ratings of the extent to which partnerships were participatory. RESULTS: Partnerships seemed to become more participatory over time. Each site developed distinctive programs with variation in fidelity to original program goals. Challenges included developing trust and maintaining racial diversity in local program leadership. CONCLUSIONS: Academics can partner with local faith communities to create unique programs that benefit the mental health of returning veterans. Research is needed to determine the effectiveness of community based programs, especially relative to typical "top-down" outreach approaches.


Subject(s)
Clergy , Community Mental Health Services/organization & administration , Community-Based Participatory Research/organization & administration , Veterans Health/statistics & numerical data , Arkansas , Community Mental Health Services/trends , Community-Based Participatory Research/trends , Humans , Public-Private Sector Partnerships , Religion and Psychology , Rural Health Services/organization & administration , Rural Health Services/trends , Veterans Health/trends , Workforce
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