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2.
J Clin Transl Sci ; 7(1): e2, 2023.
Article in English | MEDLINE | ID: mdl-36755548

ABSTRACT

Introduction: The effectiveness of community-based participatory research (CBPR) partnerships to address health inequities is well documented. CBPR integrates knowledge and perspectives of diverse communities throughout the research process, following principles that emphasize trust, power sharing, co-learning, and mutual benefits. However, institutions and funders seldom provide the time and resources needed for the critical stage of equitable partnership formation and development. Methods: Since 2011, the Detroit Urban Research Center, collaborating with other entities, has promoted the development of new community-academic research partnerships through two grant programs that combine seed funding with capacity building support from community and academic instructors/mentors experienced in CBPR. Process and outcomes were evaluated using mixed methods. Results: From 2011 to 2021, 50 partnerships received grants ranging from $2,500 to $30,000, totaling $605,000. Outcomes included equitable partnership infrastructure and processes, innovative pilot research, translation of findings to interventions and policy change, dissemination to multiple audiences, new proposals and projects, and sustained community-academic research partnerships. All partnerships continued beyond the program; over half secured additional funding. Conclusions: Keys to success included participation as community-academic teams, dedicated time for partnership/relationship development, workshops to develop equity-based skills, relationships, and projects, expert community-academic instructor guidance, and connection to additional resources. Findings demonstrate that small amounts of seed funding for newly forming community-academic partnerships, paired with capacity building support, can provide essential time and resources needed to develop diverse, inclusive, equity-focused CBPR partnerships. Building such support into funding initiatives and through academic institutions can enhance impact and sustainability of translational research toward advancing health equity.

3.
Pedagogy Health Promot ; 6(3): 168-182, 2020 Sep 01.
Article in English | MEDLINE | ID: mdl-34350338

ABSTRACT

Community-based participatory research (CBPR) is widely recognized as an effective approach to understand and address health inequities. Opportunities for public health practitioners and researchers to engage jointly with community partners in intensive colearning processes can build capacity for CBPR. Using active learning approaches that engage diverse partners can enhance partnership development, competence, and equity. Examination of such pedagogical approaches can strengthen understanding of their contributions to the effectiveness of CBPR capacity-building programs. This article describes a weeklong intensive course carried out by the Detroit Urban Research Center as the foundation for a yearlong training program to build the capacity of community-academic partnership teams to engage in CBPR in their own communities. The in-person CBPR course was developed and implemented by expert academic and community instructors and used an experiential action learning model that integrated CBPR principles and processes. We describe the course content and application of our collaborative, experiential action learning model to course design; present results from participant evaluation of course effectiveness, CBPR competence, and equitable partnership development; and examine the contributions of the pedagogical approach to outcomes central to successful CBPR. The participatory, formative course evaluation used multiple methods that included closed- and open-ended questionnaires to assess instructional effectiveness, participant competence on 12 core components of CBPR, and course impact on partner relationships. Evaluation findings suggest that an experiential action learning approach with attention to colearning, collaboration among diverse instructors and participants, and an environment that fosters and models equitable and trusting relationships can be effective in building CBPR capacity.

4.
Health Promot Pract ; 21(4): 552-563, 2020 07.
Article in English | MEDLINE | ID: mdl-30596283

ABSTRACT

Community-based participatory research (CBPR) is an equitable partnership approach that links academic researchers, community organizations, and public health practitioners to work together to understand and address health inequities. Although numerous educational materials on CBPR exist, few training programs develop the skills and knowledge needed to establish effective, equitable partnerships. Furthermore, there are few professional development opportunities for academic researchers, practitioners, and community members to obtain these competencies in an experiential co-learning process. In response, the Detroit Community-Academic Urban Research Center developed the CBPR Partnership Academy, an innovative, yearlong capacity-building program facilitated by experienced community and academic partners, involving an intensive short course, partnership development, grant proposal preparation and funding, mentoring, online learning forums, and networking. Three diverse cohorts (36 teams) from 18 states and 2 tribal nations have participated. We describe the rationale and components of the training program and present results from the first two cohorts. Evaluation results suggest enhanced competence and efficacy in conducting CBPR. Outcomes include partnerships established, grant proposals submitted and funded, workshops and research conducted, and findings disseminated. A community-academic partner-based, integrated, applied program can be effective for professional development and establishing innovative linkages between academics and practitioners aimed at achieving health equity.


Subject(s)
Community-Based Participatory Research , Community-Institutional Relations , Health Equity , Capacity Building , Humans , Michigan , Research Personnel
6.
Am J Community Psychol ; 51(1-2): 76-89, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22638902

ABSTRACT

Depression during the prenatal and postpartum periods is associated with poor maternal, perinatal and child outcomes. This study examines the effectiveness of a culturally and linguistically tailored, social support-based, healthy lifestyle intervention led by trained community health workers in reducing depressive symptoms among pregnant and early postpartum Latinas. A sample of 275 pregnant Latinas was randomized to the Healthy MOMs Healthy Lifestyle Intervention (MOMs) or the Healthy Pregnancy Education (control) group. More than one-third of participants were at risk for depression at baseline. MOMs participants were less likely than control group participants to be at risk for depression at follow-up. Between baseline and 6 weeks postpartum, MOMs participants experienced a significant decline in depressive symptoms; control participants experienced a marginally significant decline. For MOMs participants, most of this decline occurred during the pregnancy intervention period, a time when no change occurred for control participants. The change in depressive symptoms during this period was greater among MOMs than control participants ("intervention effect"). From baseline to postpartum, there was a significant intervention effect among non-English-speaking women only. These findings provide evidence that a community-planned, culturally tailored healthy lifestyle intervention led by community health workers can reduce depressive symptoms among pregnant, Spanish-speaking Latinas.


Subject(s)
Depression/prevention & control , Hispanic or Latino/psychology , Life Style/ethnology , Mothers/psychology , Pregnancy Complications/prevention & control , Adolescent , Adult , Community Networks , Community-Based Participatory Research , Depression/ethnology , Depression, Postpartum/prevention & control , Female , Health Promotion , Humans , Michigan , Pregnancy , Pregnancy Complications/ethnology , Pregnancy Complications/psychology , Young Adult
7.
Am J Public Health ; 101(12): 2253-60, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21680932

ABSTRACT

OBJECTIVES: We tested the effectiveness of a culturally tailored, behavioral theory-based community health worker intervention for improving glycemic control. METHODS: We used a randomized, 6-month delayed control group design among 164 African American and Latino adult participants recruited from 2 health systems in Detroit, Michigan. Our study was guided by the principles of community-based participatory research. Hemoglobin A1c (HbA1c) level was the primary outcome measure. Using an empowerment-based approach, community health workers provided participants with diabetes self-management education and regular home visits, and accompanied them to a clinic visit during the 6-month intervention period. RESULTS: Participants in the intervention group had a mean HbA1c value of 8.6% at baseline, which improved to a value of 7.8% at 6 months, for an adjusted change of -0.8 percentage points (P < .01). There was no change in mean HbA1c among the control group (8.5%). Intervention participants also had significantly greater improvements in self-reported diabetes understanding compared with the control group. CONCLUSIONS: This study contributes to the growing evidence for the effectiveness of community health workers and their role in multidisciplinary teams engaged in culturally appropriate health care delivery.


Subject(s)
Black or African American , Community Health Workers , Diabetes Mellitus, Type 2/ethnology , Hispanic or Latino , Patient Education as Topic , Self Care , Adult , Community-Based Participatory Research , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/therapy , Female , Glycated Hemoglobin/analysis , Humans , Male , Michigan , Middle Aged , Poverty , Urban Population
8.
J Urban Health ; 83(6): 1022-40, 2006 Nov.
Article in English | MEDLINE | ID: mdl-17139552

ABSTRACT

In order to address the social, physical and economic determinants of urban health, researchers, public health practitioners, and community members have turned to more comprehensive and participatory approaches to research and interventions. One such approach, community-based participatory research (CBPR) in public health, has received considerable attention over the past decade, and numerous publications have described theoretical underpinnings, values, principles and practice. Issues related to the long-term sustainability of partnerships and activities have received limited attention. The purpose of this article is to examine the experiences and lessons learned from three Urban Research Centers (URCs) in Detroit, New York City, and Seattle, which were initially established in 1995 with core support from the Centers for Disease Control and Prevention (CDC). The experience of these Centers after core funding ceased in 2003 provides a case study to identify the challenges and facilitating factors for sustaining partnerships. We examine three broad dimensions of CBPR partnerships that we consider important for sustainability: (1) sustaining relationships and commitments among the partners involved; (2) sustaining the knowledge, capacity and values generated from the partnership; and (3) sustaining funding, staff, programs, policy changes and the partnership itself. We discuss the challenges faced by the URCs in sustaining these dimensions and the strategies used to overcome these challenges. Based on these experiences, we offer recommendations for: strategies that partnerships may find useful in sustaining their CBPR efforts; ways in which a Center mechanism can be useful for promoting sustainability; and considerations for funders of CBPR to increase sustainability.


Subject(s)
Community Participation/methods , Community-Institutional Relations , Health Services Research/organization & administration , Urban Health Services/organization & administration , Centers for Disease Control and Prevention, U.S./organization & administration , Ethnicity , Health Services Research/economics , Humans , Racial Groups , Research Support as Topic/organization & administration , United States/epidemiology , Urban Health , Urban Health Services/economics
9.
Am J Public Health ; 96(12): 2201-8, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17077395

ABSTRACT

OBJECTIVES: We assessed the influence of maternal anthropometric and metabolic variables, including glucose tolerance, on infant birthweight. METHODS: In our prospective, population-based cohort study of 1041 Latino mother-infant pairs, we used standardized interviews, anthropometry, metabolic assays, and medical record reviews. We assessed relationships among maternal sociodemographic, prenatal care, anthropometric, and metabolic characteristics and birthweight with analysis of variance and bivariate and multivariate linear regression analyses. RESULTS: Forty-two percent of women in this study entered pregnancy overweight or obese; at least 36% exceeded weight-gain recommendations. Twenty-seven percent of the women had at least some degree of glucose abnormality, including 6.8% who had gestational diabetes. Maternal multiparity, height, weight, weight gain, and 1-hour screening glucose levels were significant independent predictors of infant birthweight after adjustment for gestational age. CONCLUSION: Studies of birthweight should account for maternal glucose level. Given the increased risk of adverse maternal and infant outcomes associated with excessive maternal weight, weight gain, and glucose intolerance, and the high prevalence of these conditions and type 2 diabetes among Latinas, public health professionals have unique opportunities for prevention through prenatal and postpartum interventions.


Subject(s)
Birth Weight/physiology , Diabetes, Gestational/ethnology , Glucose Intolerance/ethnology , Maternal Welfare/ethnology , Mexican Americans/statistics & numerical data , Obesity/ethnology , Prenatal Nutritional Physiological Phenomena/ethnology , Risk Assessment , Weight Gain/ethnology , Adult , Anthropometry , Diabetes, Gestational/metabolism , Diabetes, Gestational/physiopathology , Female , Glucose Intolerance/metabolism , Glucose Intolerance/physiopathology , Humans , Infant, Newborn , Maternal Welfare/classification , Mexico/ethnology , Michigan/epidemiology , Obesity/metabolism , Obesity/physiopathology , Pregnancy , Prenatal Care , Prevalence , Prospective Studies , Risk Factors , Socioeconomic Factors , Weight Gain/physiology
10.
J Health Care Poor Underserved ; 17(2 Suppl): 88-105, 2006 May.
Article in English | MEDLINE | ID: mdl-16809877

ABSTRACT

This study examines baseline levels and correlates of diabetes-related emotional distress among inner-city African Americans and Hispanics with type 2 diabetes. The Problem Areas in Diabetes (PAID) scale, which measures diabetes-related emotional distress, was administered to 180 African American and Hispanic adults participating in the REACH Detroit Partnership. We examined bivariate and multivariate associations between emotional distress and biological, psychosocial, and quality of health care variables for African Americans and Hispanics. Scores were significantly higher among Hispanics than African Americans. Demographic factors were stronger predictors of emotional distress for Hispanics than for African Americans. Daily hassles, physician support, and perceived seriousness and understanding of diabetes were significant for African Americans. Understanding the personal, family and community context of living with diabetes and conducting interventions that provide support and coping strategies for self-management have important implications for reducing health disparities among disadvantaged racial and ethnic groups.


Subject(s)
Black or African American/psychology , Depression/ethnology , Diabetes Mellitus, Type 2/ethnology , Diabetes Mellitus, Type 2/psychology , Healthy People Programs/organization & administration , Hispanic or Latino/psychology , Sickness Impact Profile , Urban Health , Adult , Black or African American/education , Behavioral Risk Factor Surveillance System , Depression/etiology , Diabetes Mellitus, Type 2/physiopathology , Female , Hispanic or Latino/education , Humans , Male , Michigan , Middle Aged , Pain/etiology , Pain/psychology , Quality of Health Care , Self Care , Socioeconomic Factors , Stress, Psychological/ethnology , Stress, Psychological/etiology
11.
Ethn Dis ; 14(3 Suppl 1): S27-37, 2004.
Article in English | MEDLINE | ID: mdl-15682769

ABSTRACT

Diabetes is prevalent among African-American and Latino Detroit residents, with profound consequences to individuals, families, and communities. The REACH Detroit Partnership engaged eastside and southwest Detroit families in focus groups organized by community, age, gender, and language, to plan community-based participatory interventions to reduce the prevalence and impact of diabetes and its risk factors. Community residents participated in planning, implementing, and analyzing data from the focus groups and subsequent planning meetings. Major themes included: 1) diabetes is widespread and risk begins in childhood, with severe consequences for African Americans and Latinos; 2) denial and inadequate health care contribute to lack of public awareness about pre-symptomatic diabetes; 3) diabetes risks include heredity, high sugar, fat and alcohol intake, overweight, lack of exercise, and stress; and 4) cultural traditions, lack of motivation, and lack of affordable, accessible stores, restaurants, and recreation facilities and programs, are barriers to adopting preventive lifestyles. Participants identified community assets and made recommendations that resulted in REACH Detroit's multi-level intervention design and programs. They included development of: 1) family-oriented interventions to support lifestyle change at all ages; 2) culturally relevant community and health provider education and materials; 3) social support group activities promoting diabetes self-management, exercise, and healthy eating; and 4) community resource development and advocacy.


Subject(s)
Attitude to Health/ethnology , Black or African American , Community Health Planning/organization & administration , Community Participation , Diabetes Mellitus/ethnology , Diabetes Mellitus/prevention & control , Focus Groups , Healthy People Programs , Hispanic or Latino , Adolescent , Adult , Aged , Child , Diet , Exercise , Female , Health Care Coalitions/organization & administration , Humans , Male , Michigan , Middle Aged , Patient Education as Topic , Risk Factors , Socioeconomic Factors
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