Pub Date : 2026-01-17DOI: 10.1177/15248399251411324
Farah Kader, Stephanie Kruchten, Kimberly Collica-Cox, Charis Davidson, Dial Hewlett, Marc Campo
Throughout the COVID-19 pandemic, correctional officers not only experienced high rates of COVID-19 infection but concomitantly demonstrated low vaccine uptake and high government mistrust, placing correctional staff and the incarcerated at risk for viral transmission. To support behavioral change, a multi-pronged dialogic health education intervention was developed for correctional officers in a New York county jail. One-hour facilitated discussions took place during mandatory training days. The research team collected pre- and post-surveys to assess whether the sessions impacted intention to change COVID-19 preventive behaviors, perceived effectiveness of behaviors recommended by public health professionals, and overall health literacy. Participants were also invited to participate in an interview 3-7 months after the session regarding behavior change and perceived effectiveness of the dialogic approach. Surveys were analyzed for pre-post changes, and interview notes were analyzed using thematic content analysis. The data indicate that officers were more likely to demonstrate increased health literacy and an intention to improve or maintain their non-pharmacological health behaviors following participation in a dialogue-based health information session. Outcomes suggest that when delivering sensitive health information to populations often mistrustful of governmental initiatives, information sessions that employ discussion strategies, facilitated by credible messengers, are likely to be the most effective in improving health-related knowledge and attitudes; further study is needed to understand these strategies' effect on behavioral change.
{"title":"Does Dialogue-Based Learning Motivate COVID-19 Preventive Behavior Among Correctional Officers?","authors":"Farah Kader, Stephanie Kruchten, Kimberly Collica-Cox, Charis Davidson, Dial Hewlett, Marc Campo","doi":"10.1177/15248399251411324","DOIUrl":"https://doi.org/10.1177/15248399251411324","url":null,"abstract":"<p><p>Throughout the COVID-19 pandemic, correctional officers not only experienced high rates of COVID-19 infection but concomitantly demonstrated low vaccine uptake and high government mistrust, placing correctional staff and the incarcerated at risk for viral transmission. To support behavioral change, a multi-pronged dialogic health education intervention was developed for correctional officers in a New York county jail. One-hour facilitated discussions took place during mandatory training days. The research team collected pre- and post-surveys to assess whether the sessions impacted intention to change COVID-19 preventive behaviors, perceived effectiveness of behaviors recommended by public health professionals, and overall health literacy. Participants were also invited to participate in an interview 3-7 months after the session regarding behavior change and perceived effectiveness of the dialogic approach. Surveys were analyzed for pre-post changes, and interview notes were analyzed using thematic content analysis. The data indicate that officers were more likely to demonstrate increased health literacy and an intention to improve or maintain their non-pharmacological health behaviors following participation in a dialogue-based health information session. Outcomes suggest that when delivering sensitive health information to populations often mistrustful of governmental initiatives, information sessions that employ discussion strategies, facilitated by credible messengers, are likely to be the most effective in improving health-related knowledge and attitudes; further study is needed to understand these strategies' effect on behavioral change.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"15248399251411324"},"PeriodicalIF":1.2,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145991450","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1177/15248399251411252
Mark Frank, Stephen Papagiotas, Taran Pierce, Sherrie Bruce, Stephanie Dopson
The Chief of Staff (CoS) position, in both the public and private sectors, assists the executive team in strategizing, communicating, and making decisions for the organization. The Centers for Disease Control and Prevention uses the model of a CoS within its incident management system (IMS) for public health emergency responses. During those responses, the CoS is responsible for the oversight and coordination of the operational and management functions, and that position is a primary member of the response leadership team. An effective CoS leverages their knowledge of systems and processes, resources, and subject matter expertise from across the organization to solve operational challenges. The position also facilitates connections with other federal response agencies, nongovernmental organizations, and international and domestic partners. Health departments seeking to improve how their organization addresses routine and unexpected challenges during emergency responses could consider adding a CoS role to their IMS.
{"title":"The Role of a Chief of Staff in an Incident Management System During Public Health Responses.","authors":"Mark Frank, Stephen Papagiotas, Taran Pierce, Sherrie Bruce, Stephanie Dopson","doi":"10.1177/15248399251411252","DOIUrl":"10.1177/15248399251411252","url":null,"abstract":"<p><p>The Chief of Staff (CoS) position, in both the public and private sectors, assists the executive team in strategizing, communicating, and making decisions for the organization. The Centers for Disease Control and Prevention uses the model of a CoS within its incident management system (IMS) for public health emergency responses. During those responses, the CoS is responsible for the oversight and coordination of the operational and management functions, and that position is a primary member of the response leadership team. An effective CoS leverages their knowledge of systems and processes, resources, and subject matter expertise from across the organization to solve operational challenges. The position also facilitates connections with other federal response agencies, nongovernmental organizations, and international and domestic partners. Health departments seeking to improve how their organization addresses routine and unexpected challenges during emergency responses could consider adding a CoS role to their IMS.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"15248399251411252"},"PeriodicalIF":1.2,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145960310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-13DOI: 10.1177/15248399251411326
Nichola Driver, Lucy Burgess, Becca Bona, Katie George
Medicare Annual Wellness Visits (AWVs) are yearly appointments with a PCP aimed at preventing disease or disability, based on current health and risk factors. Despite the benefits of AWVs, utilization remains low, particularly in rural states like Arkansas. This study aims to better understand the low utilization by exploring the awareness and perception of AWVs among older Arkansans. The research team conducted 9 focus groups with 96 Medicare-enrolled Arkansans. The researchers utilized an inductive thematic coding process with multiple coders for analyzing the focus group transcripts. Results suggest that Arkansans were largely unaware of AWVs. Participants saw the visits as repetitive and burdensome, did not understand their benefits, and did not understand how they differed from routine physicals. Encouragement from providers helped motivate utilization. Some specific aspects of AWVs were highlighted as useful and beneficial, such as the cognitive assessments. Still, some participants had fear, anxiety, or distrust related to the cognitive assessments. We recommend the utilization of these findings in designing messaging and awareness campaigns around AWVs and encouragement of provider promotion.
{"title":"Awareness and Perceptions of Medicare Annual Wellness Visits Among Older Adults in Arkansas.","authors":"Nichola Driver, Lucy Burgess, Becca Bona, Katie George","doi":"10.1177/15248399251411326","DOIUrl":"https://doi.org/10.1177/15248399251411326","url":null,"abstract":"<p><p>Medicare Annual Wellness Visits (AWVs) are yearly appointments with a PCP aimed at preventing disease or disability, based on current health and risk factors. Despite the benefits of AWVs, utilization remains low, particularly in rural states like Arkansas. This study aims to better understand the low utilization by exploring the awareness and perception of AWVs among older Arkansans. The research team conducted 9 focus groups with 96 Medicare-enrolled Arkansans. The researchers utilized an inductive thematic coding process with multiple coders for analyzing the focus group transcripts. Results suggest that Arkansans were largely unaware of AWVs. Participants saw the visits as repetitive and burdensome, did not understand their benefits, and did not understand how they differed from routine physicals. Encouragement from providers helped motivate utilization. Some specific aspects of AWVs were highlighted as useful and beneficial, such as the cognitive assessments. Still, some participants had fear, anxiety, or distrust related to the cognitive assessments. We recommend the utilization of these findings in designing messaging and awareness campaigns around AWVs and encouragement of provider promotion.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"15248399251411326"},"PeriodicalIF":1.2,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145960368","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-12DOI: 10.1177/15248399251411323
Chaitra Surapaneni, Linnie LaMaster, Tammy Miller
Many young people in the United States lack the exposure, confidence, and skills necessary to use public transportation independently. Our nonprofit in Austin, Texas addresses this gap by integrating daily public transit use into its summer camp experience. Each day, children (campers) and teens (volunteers) receive training and are led by camp leaders through the city using public transportation to reach educational destinations. This hands-on approach aligns with experiential learning theory, which emphasizes learning through action and reflection. It also reflects the PRECEDE-PROCEED model, prioritizing a real community need-low youth transit engagement-by reducing barriers and embedding evaluation into program design. The program builds practical navigation skills, city awareness, independence, and social confidence. Both age groups benefit: children develop early transit literacy, while teens gain leadership skills, practical knowledge, and increased civic engagement. Teaching youth to use public transportation increases the likelihood of confident, regular adult transit use, shaping future riders and strengthening public transit systems.
{"title":"Building Transit Confidence: A Nonprofit Summer Camp's Approach to Youth Transportation Literacy in Austin.","authors":"Chaitra Surapaneni, Linnie LaMaster, Tammy Miller","doi":"10.1177/15248399251411323","DOIUrl":"https://doi.org/10.1177/15248399251411323","url":null,"abstract":"<p><p>Many young people in the United States lack the exposure, confidence, and skills necessary to use public transportation independently. Our nonprofit in Austin, Texas addresses this gap by integrating daily public transit use into its summer camp experience. Each day, children (campers) and teens (volunteers) receive training and are led by camp leaders through the city using public transportation to reach educational destinations. This hands-on approach aligns with experiential learning theory, which emphasizes learning through action and reflection. It also reflects the PRECEDE-PROCEED model, prioritizing a real community need-low youth transit engagement-by reducing barriers and embedding evaluation into program design. The program builds practical navigation skills, city awareness, independence, and social confidence. Both age groups benefit: children develop early transit literacy, while teens gain leadership skills, practical knowledge, and increased civic engagement. Teaching youth to use public transportation increases the likelihood of confident, regular adult transit use, shaping future riders and strengthening public transit systems.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"15248399251411323"},"PeriodicalIF":1.2,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145953575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-01-23DOI: 10.1177/15248399241311287
C M McGhee, Brayden A Misiolek, Shanna K Kattari, Caitlin A Tupper, Lyle Chalker
The U.S. trans/gender diverse (TGD) community experiences considerable mental health disparities and barriers to health care. To address these challenges, Trans Wellness, Trans Brilliance (TWTB) was developed to advance the resilience, self-compassion, and community connectedness of TGD people in Michigan. Designed by TGD people for TGD people, this community-based research project was a joint partnership between a local trans community care organization and a large Midwestern research institution, supported by state foundation funding. The construction of TWTB was sequential and iterative. The project concept originally emerged from previous research, which identified a need for a program to enhance resilience, capacity, and emotional well-being in the broader Michigan TGD community. This led to the innovative idea of designing an intervention that was both virtually accessible and capable of being implemented by any community advocate, regardless of professional training. Interviews were conducted with community stakeholders statewide to identify the needs, desired skills, and objectives for such a skill-based program. Findings from these interviews were used to design the online intervention. Community members further shaped the intervention through a focus group, which assessed the desirability and anticipated effectiveness of the curriculum. The final product was TWTB: an 8-week, peer-support, virtual wellness intervention.
美国跨性别/性别多样化(TGD)社区经历了相当大的心理健康差异和卫生保健障碍。为了应对这些挑战,Trans Wellness, Trans Brilliance (TWTB)被开发出来,以提高密歇根州TGD患者的复原力、自我同情和社区联系。这个以社区为基础的研究项目是由TGD人为TGD人设计的,是当地跨性别社区护理组织和中西部一家大型研究机构的联合伙伴关系,由国家基金会资助。TWTB的构建是连续的、迭代的。该项目的概念最初来自于之前的研究,该研究确定了需要一个项目来增强更广泛的密歇根TGD社区的恢复力、能力和情感健康。这导致了一种创新的想法,即设计一种干预措施,这种干预措施实际上是可获得的,并且能够被任何社区倡导者实施,而不需要专业培训。与全州的社区利益相关者进行了访谈,以确定这种以技能为基础的计划的需求、所需技能和目标。这些访谈的结果被用于设计在线干预。社区成员通过焦点小组进一步形成了干预措施,该小组评估了课程的可取性和预期有效性。最终的产品是TWTB:一项为期8周、同伴支持的虚拟健康干预。
{"title":"Developing <i>Trans Wellness, Trans Brilliance</i>: A Virtual Peer-Support Wellness Intervention by and for Trans/Gender Diverse Michiganders.","authors":"C M McGhee, Brayden A Misiolek, Shanna K Kattari, Caitlin A Tupper, Lyle Chalker","doi":"10.1177/15248399241311287","DOIUrl":"10.1177/15248399241311287","url":null,"abstract":"<p><p>The U.S. trans/gender diverse (TGD) community experiences considerable mental health disparities and barriers to health care. To address these challenges, <i>Trans Wellness</i>, <i>Trans Brilliance</i> (<i>TWTB</i>) was developed to advance the resilience, self-compassion, and community connectedness of TGD people in Michigan. Designed by TGD people for TGD people, this community-based research project was a joint partnership between a local trans community care organization and a large Midwestern research institution, supported by state foundation funding. The construction of <i>TWTB</i> was sequential and iterative. The project concept originally emerged from previous research, which identified a need for a program to enhance resilience, capacity, and emotional well-being in the broader Michigan TGD community. This led to the innovative idea of designing an intervention that was both virtually accessible and capable of being implemented by any community advocate, regardless of professional training. Interviews were conducted with community stakeholders statewide to identify the needs, desired skills, and objectives for such a skill-based program. Findings from these interviews were used to design the online intervention. Community members further shaped the intervention through a focus group, which assessed the desirability and anticipated effectiveness of the curriculum. The final product was <i>TWTB</i>: an 8-week, peer-support, virtual wellness intervention.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"65-73"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143025332","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2024-05-07DOI: 10.1177/15248399241252801
Trina C Salm Ward, Terri J Miller
The Georgia Department of Public Health developed the Safe Sleep Shelter Program to expand Georgia Safe to Sleep campaign efforts. The program focused on engaging with housing support agencies, homeless shelters, and domestic violence shelters. The program offered a menu of resources that agencies could choose from, including portable cribs for agency use and distribution to families, safe sleep education for staff, assistance with creating/updating agency safe sleep policies, and Baby Bundle Safe Sleep kits with education and resources for families. The program showed promising results: 44 agencies across the state applied, serving an estimated 20,950 individuals annually. Agencies expressed strong interest in expanding safe sleep education and resources for the families they served. Most agencies reported that the program filled gaps in services, including having enough cribs to meet demand and limited safe sleep education and resources. Agencies reported that parents appreciated the cribs and Baby Bundle Safe Sleep kits as most did not have money to purchase an infant sleep surface. Agencies reported that the resources provided new information to infant parents, facilitated discussion, and reinforced safe sleep messaging. Evaluation challenges included difficulties collecting distribution data and a low response rate for parent surveys. Implications are discussed for others interested in implementing such a program, including to develop processes for communicating updated recommendations, leverage existing relationships to engage additional agencies, evaluate efforts to refine program components, and consider strategies to increase parent survey response rates.
{"title":"Implementing a Safe Sleep Shelter and Baby Bundle Kit Distribution Program.","authors":"Trina C Salm Ward, Terri J Miller","doi":"10.1177/15248399241252801","DOIUrl":"10.1177/15248399241252801","url":null,"abstract":"<p><p>The Georgia Department of Public Health developed the Safe Sleep Shelter Program to expand Georgia Safe to Sleep campaign efforts. The program focused on engaging with housing support agencies, homeless shelters, and domestic violence shelters. The program offered a menu of resources that agencies could choose from, including portable cribs for agency use and distribution to families, safe sleep education for staff, assistance with creating/updating agency safe sleep policies, and Baby Bundle Safe Sleep kits with education and resources for families. The program showed promising results: 44 agencies across the state applied, serving an estimated 20,950 individuals annually. Agencies expressed strong interest in expanding safe sleep education and resources for the families they served. Most agencies reported that the program filled gaps in services, including having enough cribs to meet demand and limited safe sleep education and resources. Agencies reported that parents appreciated the cribs and Baby Bundle Safe Sleep kits as most did not have money to purchase an infant sleep surface. Agencies reported that the resources provided new information to infant parents, facilitated discussion, and reinforced safe sleep messaging. Evaluation challenges included difficulties collecting distribution data and a low response rate for parent surveys. Implications are discussed for others interested in implementing such a program, including to develop processes for communicating updated recommendations, leverage existing relationships to engage additional agencies, evaluate efforts to refine program components, and consider strategies to increase parent survey response rates.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"13-16"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140877660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2024-11-08DOI: 10.1177/15248399241294238
Bhibha M Das, Kelsey C Simpson, Lauren R Sastre
Eastern North Carolina (ENC) residents have higher rates of type 2 diabetes, lower life expectancy, less physical activity (PA), and higher food insecurity than the rest of North Carolina. Black individuals in ENC may face health disparities due to systemic and societal barriers to PA and a nutritious diet; modifiable behaviors that may improve overall health. The purpose of this study was to explore the lived experiences of rural Black women who live in ENC and who meet the criteria for overweight and obesity in the context of PA and healthful diet promotion. Photo-elicitation was used to explore this population's specific experiences with PA and nutrition, including barriers and facilitators, through photos and focus groups. Participants (N = 14; 43.5 ± 8.7 years old; body mass index (BMI) = 34.6 ± 5.9 kg/m2) were Black women in the rural Southeastern United States. Recruitment strategies included community outreach, listservs, social media, and word of mouth. Using photos submitted, our team conducted focus groups and completed content analyses to identify themes to tailor the development of a future health promotion program for Black women. Overarching themes were (a) Reframing the Mindset, (b) Accountability, and (c) Cultural Relativity. Findings demonstrate that Black women living in rural areas desire culturally relevant PA and nutrition programming focusing on healthy lifestyles versus weight loss. Future practice and research should utilize these findings to develop and examine the health impact of a health promotion program designed for Black women by Black women on PA levels, diet quality, and quality of life.
{"title":"Exploring Rural, Black Women's Lived Experiences With Physical Activity and Nutrition: A Photo-Elicitation Study.","authors":"Bhibha M Das, Kelsey C Simpson, Lauren R Sastre","doi":"10.1177/15248399241294238","DOIUrl":"10.1177/15248399241294238","url":null,"abstract":"<p><p>Eastern North Carolina (ENC) residents have higher rates of type 2 diabetes, lower life expectancy, less physical activity (PA), and higher food insecurity than the rest of North Carolina. Black individuals in ENC may face health disparities due to systemic and societal barriers to PA and a nutritious diet; modifiable behaviors that may improve overall health. The purpose of this study was to explore the lived experiences of rural Black women who live in ENC and who meet the criteria for overweight and obesity in the context of PA and healthful diet promotion. Photo-elicitation was used to explore this population's specific experiences with PA and nutrition, including barriers and facilitators, through photos and focus groups. Participants (N = 14; 43.5 ± 8.7 years old; body mass index (BMI) = 34.6 ± 5.9 kg/m<sup>2</sup>) were Black women in the rural Southeastern United States. Recruitment strategies included community outreach, listservs, social media, and word of mouth. Using photos submitted, our team conducted focus groups and completed content analyses to identify themes to tailor the development of a future health promotion program for Black women. Overarching themes were (a) Reframing the Mindset, (b) Accountability, and (c) Cultural Relativity. Findings demonstrate that Black women living in rural areas desire culturally relevant PA and nutrition programming focusing on healthy lifestyles versus weight loss. Future practice and research should utilize these findings to develop and examine the health impact of a health promotion program designed for Black women by Black women on PA levels, diet quality, and quality of life.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"30-35"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142606902","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-01-31DOI: 10.1177/15248399241311587
Mary Beth Deline, Mary Katreeb, Emily 'mj' Mason, Laura N Rickard, Ertemisa Godinez, Kajsa E Dalrymple
Efforts to effect racial health disparity (RHD) policy change are urgent, necessary, and subject to a key barrier: defensiveness among White privileged audiences. Within the literature to date, such defensiveness is under-investigated, and when examined, is typically conceived of as an individual cognitive outcome-a message effect-rather than a communication interaction. Yet policy change advocacy efforts, ranging from community organizing to change campaigns, necessitate communication interactions between advocates and privileged policy change audiences, such as neighborhood groups or policymakers themselves. This defensiveness conceptualization, focused on individual cognitions, therefore limits our understanding of interactive communication barriers in RHD policy advocacy processes. To address this limitation, our research conceives of defensiveness using the privileged identity exploration (PIE) model, developed by Watt in 2007, which posits that defensiveness strategies are used as part of an interactive communication process when people are asked to reflect on their own privilege. Defensiveness strategies, as described by Watt and colleagues in 2021 and 2023, are normal communicative reactions to protect one's self-identity from threatening information; the PIE models eight such strategies. RHD information invokes racial privilege, therefore eliciting defensiveness. Using a thematic analysis of semi-structured qualitative interviews with White young adults from the Chicago (U.S.) area (N = 27), we identify defensiveness strategies relative to COVID-19 RHDs. Using the PIE as a lens to understand the data, we find some strategies lacking, some similar but differently nuanced, and identify a novel strategy among our participants, suggesting message tailoring opportunities. We describe implications for future research and practice.
{"title":"Addressing Barriers to Racial Health Disparity Policy Change Advocacy: Exploring White Defensiveness Strategies.","authors":"Mary Beth Deline, Mary Katreeb, Emily 'mj' Mason, Laura N Rickard, Ertemisa Godinez, Kajsa E Dalrymple","doi":"10.1177/15248399241311587","DOIUrl":"10.1177/15248399241311587","url":null,"abstract":"<p><p>Efforts to effect racial health disparity (RHD) policy change are urgent, necessary, and subject to a key barrier: defensiveness among White privileged audiences. Within the literature to date, such defensiveness is under-investigated, and when examined, is typically conceived of as an individual cognitive outcome-a message effect-rather than a communication interaction. Yet policy change advocacy efforts, ranging from community organizing to change campaigns, necessitate communication interactions between advocates and privileged policy change audiences, such as neighborhood groups or policymakers themselves. This defensiveness conceptualization, focused on individual cognitions, therefore limits our understanding of interactive communication barriers in RHD policy advocacy processes. To address this limitation, our research conceives of defensiveness using the privileged identity exploration (PIE) model, developed by Watt in 2007, which posits that defensiveness strategies are used as part of an interactive communication process when people are asked to reflect on their own privilege. Defensiveness strategies, as described by Watt and colleagues in 2021 and 2023, are normal communicative reactions to protect one's self-identity from threatening information; the PIE models eight such strategies. RHD information invokes racial privilege, therefore eliciting defensiveness. Using a thematic analysis of semi-structured qualitative interviews with White young adults from the Chicago (U.S.) area (N = 27), we identify defensiveness strategies relative to COVID-19 RHDs. Using the PIE as a lens to understand the data, we find some strategies lacking, some similar but differently nuanced, and identify a novel strategy among our participants, suggesting message tailoring opportunities. We describe implications for future research and practice.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"113-122"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12738969/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143068924","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-03-23DOI: 10.1177/15248399251323901
Noah Lenstra, Pam B DeGuzman, Rozalynd McConnaughy, Megan Weis
During the past decade, public libraries have been framed as key health promotion partners for everything from telemedicine to the opioid crisis. This study's goal was to evaluate the impacts of health promotion initiatives involving public libraries as collaborators. Using preferred reporting items for systematic reviews and meta-analyses (PRISMA) guidelines, a search of three databases (PubMed, CINAHL Complete, and Library and information science abstracts (LISA)) for articles written in English referencing "health" and "public libraries" returned 985 unique citations, of which 67 papers were selected for review, based on the criteria of being peer-reviewed articles on health initiatives involving public libraries. All studies were published between 1957 and 2023, with 88% published in the 2000's, and 76% conducted in the United States. Most studies consisted of descriptive accounts of health promotion initiatives, with minimal reporting of outcome measures for the populations targeted. Better understanding the impacts of health promotion initiatives involving public libraries requires more rigorous assessment mechanisms, and the long-term success of these partnerships depends on stronger and sustained linkages between those working in health and those working in libraries, particularly public libraries.
{"title":"How Do Public Library Partnerships Impact Health? A Scoping Review.","authors":"Noah Lenstra, Pam B DeGuzman, Rozalynd McConnaughy, Megan Weis","doi":"10.1177/15248399251323901","DOIUrl":"10.1177/15248399251323901","url":null,"abstract":"<p><p>During the past decade, public libraries have been framed as key health promotion partners for everything from telemedicine to the opioid crisis. This study's goal was to evaluate the impacts of health promotion initiatives involving public libraries as collaborators. Using preferred reporting items for systematic reviews and meta-analyses (PRISMA) guidelines, a search of three databases (PubMed, CINAHL Complete, and Library and information science abstracts (LISA)) for articles written in English referencing \"health\" and \"public libraries\" returned 985 unique citations, of which 67 papers were selected for review, based on the criteria of being peer-reviewed articles on health initiatives involving public libraries. All studies were published between 1957 and 2023, with 88% published in the 2000's, and 76% conducted in the United States. Most studies consisted of descriptive accounts of health promotion initiatives, with minimal reporting of outcome measures for the populations targeted. Better understanding the impacts of health promotion initiatives involving public libraries requires more rigorous assessment mechanisms, and the long-term success of these partnerships depends on stronger and sustained linkages between those working in health and those working in libraries, particularly public libraries.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"173-191"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143693960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2024-12-23DOI: 10.1177/15248399241306409
Ginny E Kincaid, Carolyn Headley, Anna Jaffee, Bria Marlowe, Ally Moehring, Will A Murphy, Laura K Vercammen
Shifts in colorectal cancer (CRC) screening, including guidance from the United States Preventive Services Task Force lowering the recommended screening age from 50 to 45 years in 2021, may leave gaps in clinicians' understanding of related barriers and beliefs held by patients. This study uses the National Institute on Minority Health and Health Disparities Research Framework to analyze factors influencing CRC screening uptake among individuals aged 44-54 years and identifies how gaps in knowledge intersect with screening barriers, particularly as they relate to the health care system and sociocultural environment. In 2022, the Centers for Disease Control and Prevention's Division of Cancer Prevention and Control's Screen for Life campaign conducted 12 online focus groups to gather audience insights and test materials. Researchers conducted the focus groups in English and Spanish with individuals aged 44-54 years who had never had CRC and had never received a CRC screening. Focus groups gauged participants' knowledge, awareness, and behavior pertaining to CRC and CRC screening. Results show that participants often lacked knowledge about risk factors and screening modalities and appreciated emotionally resonant communication approaches that addressed gaps in knowledge using demystifying, destigmatizing language and representative imagery. Findings also indicate a need to help patients overcome barriers related to insurance coverage, treatment options, and discrimination. Results may guide the development of future health promotion efforts and empower health care providers to approach conversations with their patients with additional context regarding patients' needs.
结直肠癌(CRC)筛查的转变,包括美国预防服务工作组(United States Preventive Services Task Force)在2021年将推荐筛查年龄从50岁降低到45岁的指南,可能会在临床医生对相关障碍和患者持有的信念的理解上留下空白。本研究使用国家少数民族健康和健康差异研究框架研究所来分析影响44-54岁人群CRC筛查的因素,并确定知识差距如何与筛查障碍相交,特别是当它们与卫生保健系统和社会文化环境相关时。2022年,美国疾病控制与预防中心癌症预防与控制部门的“生命筛查”活动开展了12个在线焦点小组,以收集受众的见解和测试材料。研究人员用英语和西班牙语对44-54岁从未患过结直肠癌且从未接受过结直肠癌筛查的个体进行了焦点小组研究。焦点小组评估参与者关于CRC和CRC筛查的知识、意识和行为。结果表明,参与者往往缺乏对风险因素和筛查方式的了解,并欣赏情感共鸣的沟通方式,这些沟通方式使用去神秘化、去污名化的语言和代表性图像来解决知识差距。研究结果还表明,需要帮助患者克服与保险范围、治疗选择和歧视有关的障碍。结果可以指导未来健康促进工作的发展,并授权卫生保健提供者在与患者进行对话时考虑患者需求的额外背景。
{"title":"Colorectal Cancer Messaging and Gaps in Knowledge Among Screening-Eligible Individuals.","authors":"Ginny E Kincaid, Carolyn Headley, Anna Jaffee, Bria Marlowe, Ally Moehring, Will A Murphy, Laura K Vercammen","doi":"10.1177/15248399241306409","DOIUrl":"10.1177/15248399241306409","url":null,"abstract":"<p><p>Shifts in colorectal cancer (CRC) screening, including guidance from the United States Preventive Services Task Force lowering the recommended screening age from 50 to 45 years in 2021, may leave gaps in clinicians' understanding of related barriers and beliefs held by patients. This study uses the National Institute on Minority Health and Health Disparities Research Framework to analyze factors influencing CRC screening uptake among individuals aged 44-54 years and identifies how gaps in knowledge intersect with screening barriers, particularly as they relate to the health care system and sociocultural environment. In 2022, the Centers for Disease Control and Prevention's Division of Cancer Prevention and Control's Screen for Life campaign conducted 12 online focus groups to gather audience insights and test materials. Researchers conducted the focus groups in English and Spanish with individuals aged 44-54 years who had never had CRC and had never received a CRC screening. Focus groups gauged participants' knowledge, awareness, and behavior pertaining to CRC and CRC screening. Results show that participants often lacked knowledge about risk factors and screening modalities and appreciated emotionally resonant communication approaches that addressed gaps in knowledge using demystifying, destigmatizing language and representative imagery. Findings also indicate a need to help patients overcome barriers related to insurance coverage, treatment options, and discrimination. Results may guide the development of future health promotion efforts and empower health care providers to approach conversations with their patients with additional context regarding patients' needs.</p>","PeriodicalId":47956,"journal":{"name":"Health Promotion Practice","volume":" ","pages":"94-102"},"PeriodicalIF":1.2,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12183314/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142883318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}