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1.
Ethn Health ; 24(5): 560-574, 2019 07.
Article in English | MEDLINE | ID: mdl-28670980

ABSTRACT

OBJECTIVES: Despite the disproportionately high rates of heterosexually transmitted HIV infection among US Blacks and ongoing need for effective inexpensive behavioral interventions, the use of sermons as an HIV prevention tool in Black churches has received little research attention. The Black church plays an important role in Black communities and is a potential ally in development and delivery of sexual risk prevention messages. The objective of this study was to examine Black pastors' thoughts about whether sermons should address issues related to heterosexual relationships - and the barriers and facilitators to discussing these topics in a sermon setting. DESIGN: We conducted in-depth semi-structured, individual interviews among 39 pastors of Black churches in North Carolina and analyzed the interview data using thematic analysis strategies based on grounded theory. RESULTS: Pastors expressed widely ranging opinions, especially about discussion of condom use, but generally agreed that sermons should discuss marriage, abstinence, monogamy, dating, and infidelity - behaviors that impact sexual networks and HIV transmission. The major barriers to incorporation of these subjects into sermons include the extent to which a concept undermines their religious beliefs and uncertainty about how to incorporate it. However, scriptural support for a prevention message and the pastor's perception that the message is relevant to the congregation facilitate incorporation of related topics into sermons. CONCLUSIONS: These findings have implications for the potential utility of sermons as an HIV prevention tool and suggest that it is possible for public health professionals and pastors of Black churches to form partnerships to develop messages that are consonant with pastors' religious convictions as well as public health recommendations.


Subject(s)
Black or African American , Christianity , Clergy , HIV Infections/prevention & control , Sexual Behavior , Adolescent , Adult , Bible , Condoms , Female , HIV Infections/ethnology , Humans , Interviews as Topic , Male , Marriage , Middle Aged , North Carolina , Sexual Abstinence , Young Adult
2.
Am J Health Promot ; 31(6): 465-475, 2017 Nov.
Article in English | MEDLINE | ID: mdl-29065713

ABSTRACT

PURPOSE: Parents and caregivers play an important role in sexual socialization of youth, often serving as the primary source of information about sex. For African American rural youth who experience disparate rates of HIV/sexually transmitted infection, improving caregiver-youth communication about sexual topics may help to reduce risky behaviors. This study assessed the impact of an intervention to improve sexual topic communication. DESIGN: A Preintervention-postintervention, quasi-experimental, controlled, and community-based trial. SETTING: Intervention was in 2 rural North Carolina counties with comparison group in 3 adjacent counties. SUBJECTS: Participants (n = 249) were parents, caregivers, or parental figures for African American youth aged 10 to 14. INTERVENTION: Twelve-session curriculum for participating dyads. MEASURES: Audio computer-assisted self-interview to assess changes at 9 months from baseline in communication about general and sensitive sex topics and overall communication about sex. ANALYSIS: Multivariable models were used to examine the differences between the changes in mean of scores for intervention and comparison groups. RESULTS: Statistically significant differences in changes in mean scores for communication about general sex topics ( P < .0001), communication about sensitive sex topics ( P < .0001), and overall communication about sex ( P < .0001) existed. Differences in change in mean scores remained significant after adjusting baseline scores and other variables in the multivariate models. CONCLUSIONS: In Teach One Reach One intervention, adult participants reported improved communication about sex, an important element to support risk reduction among youth in high-prevalence areas.


Subject(s)
HIV Infections/prevention & control , Parent-Child Relations , Sex Education , Sexually Transmitted Diseases/prevention & control , Adolescent , Adult , Black or African American/psychology , Child , Communication , Controlled Before-After Studies , Cost of Illness , Female , Health Knowledge, Attitudes, Practice , Humans , Male , North Carolina , Program Evaluation , Sex Education/methods
3.
Prog Community Health Partnersh ; 9(3): 413-22, 2015.
Article in English | MEDLINE | ID: mdl-26548793

ABSTRACT

BACKGROUND: Data collection and data management (DCDM) within community-engaged research (CEnR) requires special considerations that differ from those of traditional research. To date, little guidance exists to preemptively help community-academic partnerships anticipate and resolve DCDM issues that may arise. OBJECTIVE: We sought to provide recommendations for DCDM based on two CEnR research projects. METHODS: We used a case study design to describe the DCDM process and lessons learned that were generated through formal and informal discussions between community and academic partners. LESSONS LEARNED: We identified 4 key lessons: 1) CEnR requires a flexible, iterative approach to DCDM, 2) there are trade-offs to having a flexible DCDM approach, 3) responsibilities for DCDM should consider the skill sets and priorities of all partners, and 4) nuances of DC within CEnR has important implications for human subjects and ethics training. CONCLUSIONS: Based on our lessons learned, we provide recommendations for how to approach DCDM within CEnR.


Subject(s)
Community-Based Participatory Research/methods , Community-Institutional Relations , Data Collection/methods , Health Information Management/methods , Health Services Needs and Demand , Health Status Disparities , Humans , North Carolina , Public Health/methods , Rural Population
4.
Diabetes Educ ; 39(6): 776-85, 2013.
Article in English | MEDLINE | ID: mdl-24129595

ABSTRACT

PURPOSE: The purpose of this study was to describe the feasibility of using a community-based participatory research (CBPR) approach to implement the Power to Prevent (P2P) diabetes prevention education curriculum in rural African American (AA) settings. METHODS: Trained community health workers facilitated the 12-session P2P curriculum across 3 community settings. Quantitative (based on the pre- and post-curriculum questionnaires and changes in blood glucose, blood pressure [BP], and weight at baseline and 6 months) and qualitative data (based on semi-structured interviews with facilitators) were collected. Indicators of feasibility included: demand, acceptability, implementation fidelity, and limited efficacy testing. RESULTS: Across 3 counties, 104 AA participants were recruited; 43% completed ≥ 75% of the sessions. There was great demand for the program. Fifteen community health ambassadors (CHAs) were trained, and 4 served as curriculum facilitators. Content and structure of the intervention was acceptable to facilitators but there were challenges to implementing the program as designed. Improvements were seen in diabetes knowledge and the impact of healthy eating and physical activity on diabetes prevention, but there were no significant changes in blood glucose, BP, or weight. CONCLUSION: While it is feasible to use a CBPR approach to recruit participants and implement the P2P curriculum in AA community settings, there are significant challenges that must be overcome.


Subject(s)
Black or African American , Diabetes Mellitus, Type 2/prevention & control , Health Behavior , Health Education , Obesity/prevention & control , Patient Acceptance of Health Care/statistics & numerical data , Self Care , Adult , Aged , Aged, 80 and over , Black People , Blood Glucose/metabolism , Blood Pressure , Body Mass Index , Community Health Services , Community Health Workers , Community-Based Participatory Research , Curriculum , Diabetes Mellitus, Type 2/ethnology , Diabetes Mellitus, Type 2/psychology , Feasibility Studies , Female , Health Behavior/ethnology , Health Education/organization & administration , Humans , Male , Middle Aged , Obesity/ethnology , Patient Acceptance of Health Care/ethnology , Patient Acceptance of Health Care/psychology , Patient Education as Topic , Program Evaluation , Religion and Medicine , Rural Population , Self Care/psychology , Self Care/statistics & numerical data , Weight Loss
5.
Prog Community Health Partnersh ; 7(3): 263-70, 2013.
Article in English | MEDLINE | ID: mdl-24056508

ABSTRACT

BACKGROUND: Community-based participatory research (CBPR) strives for equitable collaboration among community and academic partners throughout the research process. To build the capacity of academia to function as effective research partners with communities, the North Carolina Translational and Clinical Sciences Institute (NC TraCS), home of the University of North Carolina at Chapel Hill (UNC-CH)'s Clinical and Translational Sciences Award (CTSA), developed a community engagement consulting model. This new model harnesses the expertise of community partners with CBPR experience and compensates them equitably to provide technical assistance to community-academic research partnerships. OBJECTIVES: This paper describes approaches to valuing community expertise, the importance of equitable compensation for community partners, the impact on the community partners, opportunities for institutional change, and the constraints faced in model implementation. METHODS: Community Experts (CEs) are independent contractor consultants. CEs were interviewed to evaluate their satisfaction with their engagement and compensation for their work. LESSONS LEARNED: (1) CEs have knowledge, power, and credibility to push for systems change. (2) Changes were needed within the university to facilitate successful consultation to community-academic partnerships. (3) Sustaining the CE role requires staff support, continued compensation, increased opportunities for engagement, and careful consideration of position demands. (4) The role provides benefits beyond financial compensation. (5) Opportunities to gather deepened relationships within the partnership and built collective knowledge that strengthened the project. CONCLUSIONS: Leveraging CE expertise and compensating them for their role benefits both university and community. Creating a place for community expertise within academia is an important step toward equitably including the community in research.


Subject(s)
Community-Based Participatory Research , Community-Institutional Relations , Compensation and Redress , Consultants , Contract Services/economics , Capacity Building , Humans , North Carolina , Role
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