Pub Date : 2025-12-01Epub Date: 2025-03-14DOI: 10.17269/s41997-025-01011-x
Thomas Barker, Heather Allen, Karen Fulton, Nienke Klaver, Lori Motluk, Tanya Osborne, Edward Staples
Setting: A public health society working group wanted to use social marketing approaches to engage with a community and stimulate social support for a health treatment. The group struggled to collect effectiveness (summative) data during the project. To make up for this lack, the group explored ways to measure effectiveness of engagement (the primary outcome) based on written records (meeting minutes) kept during the project.
Intervention: The working group kept minutes of meetings that contained records of the level of participation of members by names. The text of 18 meetings (14,000 words) was edited so that the names of participants were replaced with roles that corresponded to working group members' roles: grassroots health advocates, community health agency representatives, and experts or knowledge leaders. The corpus was imported into a text analysis platform that measured word frequency. Results were tallied for the three categories of group member roles. To validate the method as a meaningful summative evaluation, the text analysis approach was critiqued using a developmental evaluation framework.
Outcomes: The text analysis evaluation indicated that the word frequency of "partner," (community health partner), "community" (grassroots health advocates), and "expert" (or knowledge leaders) tags began to converge as the campaign progressed. Initially, experts and community health partners spoke less in meetings, and community members spoke more. Over time, all members began contributing more equally during the meetings. The checklist evaluation indicated alignment of the technique with established evaluation protocols used in the field of public health.
Implications: The text and checklist analyses support the notion that engagement among working group members may be, and thus may be seen as, a precondition of engagement with the community. When used with evidence from event evaluations, the innovation may be used as an argument for effectiveness as an outcome in community-based public health campaigns that do not use conventional project (summative) evaluations.
{"title":"Working group engagement as a precondition of successful community engagement in an expert-led social marketing public health intervention: Learning from the footprints.","authors":"Thomas Barker, Heather Allen, Karen Fulton, Nienke Klaver, Lori Motluk, Tanya Osborne, Edward Staples","doi":"10.17269/s41997-025-01011-x","DOIUrl":"10.17269/s41997-025-01011-x","url":null,"abstract":"<p><strong>Setting: </strong>A public health society working group wanted to use social marketing approaches to engage with a community and stimulate social support for a health treatment. The group struggled to collect effectiveness (summative) data during the project. To make up for this lack, the group explored ways to measure effectiveness of engagement (the primary outcome) based on written records (meeting minutes) kept during the project.</p><p><strong>Intervention: </strong>The working group kept minutes of meetings that contained records of the level of participation of members by names. The text of 18 meetings (14,000 words) was edited so that the names of participants were replaced with roles that corresponded to working group members' roles: grassroots health advocates, community health agency representatives, and experts or knowledge leaders. The corpus was imported into a text analysis platform that measured word frequency. Results were tallied for the three categories of group member roles. To validate the method as a meaningful summative evaluation, the text analysis approach was critiqued using a developmental evaluation framework.</p><p><strong>Outcomes: </strong>The text analysis evaluation indicated that the word frequency of \"partner,\" (community health partner), \"community\" (grassroots health advocates), and \"expert\" (or knowledge leaders) tags began to converge as the campaign progressed. Initially, experts and community health partners spoke less in meetings, and community members spoke more. Over time, all members began contributing more equally during the meetings. The checklist evaluation indicated alignment of the technique with established evaluation protocols used in the field of public health.</p><p><strong>Implications: </strong>The text and checklist analyses support the notion that engagement among working group members may be, and thus may be seen as, a precondition of engagement with the community. When used with evidence from event evaluations, the innovation may be used as an argument for effectiveness as an outcome in community-based public health campaigns that do not use conventional project (summative) evaluations.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":"887-895"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12755133/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143630758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-04-16DOI: 10.17269/s41997-025-01020-w
Meaghen Quinlan-Davidson, Kristin Cleverley, Skye Barbic, Darren Courtney, Gina Dimitropoulos, Lisa D Hawke, Nadia Nandlall, Clement Ma, Matthew Prebeg, J L Henderson
Objectives: To generate concrete, youth-derived recommendations to support Canada's post-pandemic recovery from COVID-19 to support youth mental health and substance use (MHSU), economic, and educational recovery.
Methods: Using a virtual, modified Delphi, participants rated recommendation items over three rounds, with the option to create their own recommendation items. A priori consensus was defined as ≥ 70% of the entire group, or subgroups of youth (e.g., age, race/ethnicity, gender and sexual identities), rating items at a 6 or 7 (on a 7-point Likert scale). Items were dropped in subsequent rounds if they did not achieve consensus. Qualitative responses were analyzed using content analysis for Round 1.
Results: A total of 40 youths participated in Round 1, with good retention (97.5%) in subsequent rounds. Youths achieved consensus on eight recommendations to support post-pandemic recovery. Youths endorsed post-pandemic strategies that prioritize the implementation of effective, accessible, and low-cost MHSU services in schools, workplaces, and communities; the integration of MHSU education into school lessons; increased awareness about MHSU services in schools and workplaces; and the prioritization of health and well-being in schools and workplaces.
Conclusion: Findings indicate the need for stronger partnerships between schools, community-based MHSU services, and hospitals, and job opportunities that pay a living wage.
{"title":"Are we out of the woods yet? Youth-developed recommendations on recovery from the COVID-19 pandemic: A national Delphi study.","authors":"Meaghen Quinlan-Davidson, Kristin Cleverley, Skye Barbic, Darren Courtney, Gina Dimitropoulos, Lisa D Hawke, Nadia Nandlall, Clement Ma, Matthew Prebeg, J L Henderson","doi":"10.17269/s41997-025-01020-w","DOIUrl":"10.17269/s41997-025-01020-w","url":null,"abstract":"<p><strong>Objectives: </strong>To generate concrete, youth-derived recommendations to support Canada's post-pandemic recovery from COVID-19 to support youth mental health and substance use (MHSU), economic, and educational recovery.</p><p><strong>Methods: </strong>Using a virtual, modified Delphi, participants rated recommendation items over three rounds, with the option to create their own recommendation items. A priori consensus was defined as ≥ 70% of the entire group, or subgroups of youth (e.g., age, race/ethnicity, gender and sexual identities), rating items at a 6 or 7 (on a 7-point Likert scale). Items were dropped in subsequent rounds if they did not achieve consensus. Qualitative responses were analyzed using content analysis for Round 1.</p><p><strong>Results: </strong>A total of 40 youths participated in Round 1, with good retention (97.5%) in subsequent rounds. Youths achieved consensus on eight recommendations to support post-pandemic recovery. Youths endorsed post-pandemic strategies that prioritize the implementation of effective, accessible, and low-cost MHSU services in schools, workplaces, and communities; the integration of MHSU education into school lessons; increased awareness about MHSU services in schools and workplaces; and the prioritization of health and well-being in schools and workplaces.</p><p><strong>Conclusion: </strong>Findings indicate the need for stronger partnerships between schools, community-based MHSU services, and hospitals, and job opportunities that pay a living wage.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":"985-998"},"PeriodicalIF":2.6,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12753593/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144055504","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25DOI: 10.17269/s41997-025-01132-3
Shinjini Mondal, Breanna K Wodnik, Kian Rego, Garima Talwar Kapoor, Madelyn P Law, Erica Di Ruggiero
Increasing evidence suggests that public health systems governance should focus on organizational leadership competencies in addition to individual competencies to better enable collaborative, equitable, and effective public health systems. As part of a broader study, we conducted 12 interviews to understand the perspectives of public health leaders in Canada regarding the importance of focusing on organizational leadership competencies. Public health leaders viewed organizational leadership as a collective contribution that requires sustained efforts through organizations' learning environment and culture. According to informants, a focus on the organizational level can enable (1) team building and structural dismantling of inequities, (2) tailoring of leadership responses to different provincial and local contexts, and (3) the building of an ecosystem that promotes nurturing and adaptive spaces to facilitate mindset change and prevent siloing. Interviewees also emphasized the dynamic and changing nature of these competencies, particularly in light of the system-level weaknesses highlighted during the COVID-19 pandemic and the global political climate, which necessitate regular review and careful examination to ensure relevance. We conclude by calling for greater focus on organizational leadership competencies for public health governance.
{"title":"Organizational leadership competencies for effective public health systems governance: What are public health leaders in Canada saying?","authors":"Shinjini Mondal, Breanna K Wodnik, Kian Rego, Garima Talwar Kapoor, Madelyn P Law, Erica Di Ruggiero","doi":"10.17269/s41997-025-01132-3","DOIUrl":"10.17269/s41997-025-01132-3","url":null,"abstract":"<p><p>Increasing evidence suggests that public health systems governance should focus on organizational leadership competencies in addition to individual competencies to better enable collaborative, equitable, and effective public health systems. As part of a broader study, we conducted 12 interviews to understand the perspectives of public health leaders in Canada regarding the importance of focusing on organizational leadership competencies. Public health leaders viewed organizational leadership as a collective contribution that requires sustained efforts through organizations' learning environment and culture. According to informants, a focus on the organizational level can enable (1) team building and structural dismantling of inequities, (2) tailoring of leadership responses to different provincial and local contexts, and (3) the building of an ecosystem that promotes nurturing and adaptive spaces to facilitate mindset change and prevent siloing. Interviewees also emphasized the dynamic and changing nature of these competencies, particularly in light of the system-level weaknesses highlighted during the COVID-19 pandemic and the global political climate, which necessitate regular review and careful examination to ensure relevance. We conclude by calling for greater focus on organizational leadership competencies for public health governance.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145607352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-23DOI: 10.17269/s41997-025-01134-1
Wendy Pons, Negar Elmieh, Atanu Sarkar, Angelo Armijos-Carrion, Tom Chapman, Amandeep Hans, Margaret Haworth-Brockman, Stefan Iwasawa, Victoria Ng, Jullia Santos, Jade Savage, Divya Zalawadia
Setting: Climate change in Canada has expanded suitable habitats for both native and invasive mosquitoes, heightening the need for more robust and adaptable surveillance systems. Traditional surveillance methods face significant logistical and geographical challenges, particularly in remote or underserved areas, emphasizing the importance of innovative strategies that complement existing approaches.
Intervention: We developed a community-based mosquito surveillance toolkit, informed by a systematic review and validated by a multidisciplinary expert group. The toolkit includes a structured guide for developing a community science project, including how to design an effective mosquito surveillance program through data collection, volunteer engagement, and evaluation. It also features a quick reference guide and a 90-s animated video to facilitate understanding and engagement.
Outcome: The toolkit was introduced at a national community meeting, with 69 participants bringing together public health professionals, educators, scientists, and community leaders from across Canada in February 2025. Participants expressed enthusiasm for using the toolkit to enhance local monitoring efforts, and discussions at the meeting helped identify key opportunities and challenges for adoption.
Implications: Organizations and public health authorities now have a clear, evidence-based guide to designing, implementing, and evaluating community-driven initiatives. This toolkit not only helps ensure that volunteer participation is meaningful and effective, but it also enhances the capacity to respond to emerging challenges in vector control, laying the groundwork for sustainable, community-driven surveillance efforts.
{"title":"Community science for mosquito surveillance in Canada: a toolkit for program design and implementation.","authors":"Wendy Pons, Negar Elmieh, Atanu Sarkar, Angelo Armijos-Carrion, Tom Chapman, Amandeep Hans, Margaret Haworth-Brockman, Stefan Iwasawa, Victoria Ng, Jullia Santos, Jade Savage, Divya Zalawadia","doi":"10.17269/s41997-025-01134-1","DOIUrl":"https://doi.org/10.17269/s41997-025-01134-1","url":null,"abstract":"<p><strong>Setting: </strong>Climate change in Canada has expanded suitable habitats for both native and invasive mosquitoes, heightening the need for more robust and adaptable surveillance systems. Traditional surveillance methods face significant logistical and geographical challenges, particularly in remote or underserved areas, emphasizing the importance of innovative strategies that complement existing approaches.</p><p><strong>Intervention: </strong>We developed a community-based mosquito surveillance toolkit, informed by a systematic review and validated by a multidisciplinary expert group. The toolkit includes a structured guide for developing a community science project, including how to design an effective mosquito surveillance program through data collection, volunteer engagement, and evaluation. It also features a quick reference guide and a 90-s animated video to facilitate understanding and engagement.</p><p><strong>Outcome: </strong>The toolkit was introduced at a national community meeting, with 69 participants bringing together public health professionals, educators, scientists, and community leaders from across Canada in February 2025. Participants expressed enthusiasm for using the toolkit to enhance local monitoring efforts, and discussions at the meeting helped identify key opportunities and challenges for adoption.</p><p><strong>Implications: </strong>Organizations and public health authorities now have a clear, evidence-based guide to designing, implementing, and evaluating community-driven initiatives. This toolkit not only helps ensure that volunteer participation is meaningful and effective, but it also enhances the capacity to respond to emerging challenges in vector control, laying the groundwork for sustainable, community-driven surveillance efforts.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589586","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-23DOI: 10.17269/s41997-025-01123-4
Pegah Rahbar, Jessica J Wong, Dan Wang, Efrosini Papaconstantinou, Sheilah Hogg-Johnson, Pierre Côté
<p><strong>Objectives: </strong>Poor sleep quality's risk factors remain understudied in aging populations. Chronic back problems (CBP), a leading cause of disability, may contribute to poor sleep quality. Firstly, we determined the prevalence of poor sleep quality. Secondly, we investigated the association between chronic back problems and poor sleep quality, controlling for covariates. Lastly, we explored the interaction between sleep apnea and chronic back problems with respect to their association with poor sleep quality.</p><p><strong>Methods: </strong>We analyzed data from Ontarians ≥ 60 years in the 2015-2016 Canadian Community Health Survey. We estimated the prevalence (95% confidence interval (CI)) of poor sleep quality. We investigated the association between CBP and poor sleep quality to compute prevalence ratios (PR) and 95% CI, controlling for covariates. We explored the interaction between CBP and sleep apnea in their association with poor sleep quality using four combined exposure categories.</p><p><strong>Results: </strong>Overall, 52% of participants reported sleeping < 7 h or ≥ 9 h, 18% reported trouble going to/staying asleep, and 13% never/rarely felt refreshed. Controlling for covariates, CBP was associated with sleeping outside of recommended guidelines (PR = 1.19 (1.11-1.27)), trouble going to sleep or staying asleep (PR = 1.54 (1.32-1.79)), and rarely/never having refreshing sleep (PR = 1.45 (1.20-1.79)). No interaction was found between CBP and sleep apnea.</p><p><strong>Conclusion: </strong>We found that CBP is associated with poor sleep quality among Ontarians ≥ 60 years. Future studies should investigate CBP as a potential risk factor for poor sleep quality. Résumé Objectifs: Les facteurs de risque d'un sommeil de mauvaise qualité sont encore sous-étudiés dans les populations vieillissantes. Les problèmes de dos chroniques (PDC), l'une des principales causes d'invalidité, pourraient contribuer à la mauvaise qualité du sommeil. En premier lieu, nous avons déterminé la prévalence de la mauvaise qualité du sommeil. En deuxième lieu, nous avons étudié l'association entre les problèmes de dos chroniques et la mauvaise qualité du sommeil après avoir apporté des ajustements pour tenir compte des effets de covariables. Pour terminer, nous avons exploré l'interaction entre l'apnée du sommeil et les problèmes de dos chroniques du point de vue de leur association avec la mauvaise qualité du sommeil. Méthodes: Nous avons analysé les données d'Ontariennes et d'Ontariens de ≥ 60 ans ayant participé à l'Enquête sur la santé dans les collectivités canadiennes de 2015-2016. Nous avons estimé la prévalence (intervalle de confiance [IC] de 95%) de la mauvaise qualité du sommeil. Nous avons étudié l'association entre les PDC et la mauvaise qualité du sommeil pour calculer des ratios de prévalence (RP) et des IC de 95%, après avoir apporté des ajustements pour tenir compte des effets de covariables. Nous avons exploré l'interaction entre l
目的:老年人睡眠质量差的风险因素仍未得到充分研究。慢性背部问题(CBP)是导致残疾的主要原因,可能会导致睡眠质量差。首先,我们确定了睡眠质量差的普遍程度。其次,我们调查了慢性背部问题和睡眠质量差之间的关系,控制了协变量。最后,我们探讨了睡眠呼吸暂停和慢性背部问题之间的相互作用,以及它们与睡眠质量差的关系。方法:我们分析了2015-2016年加拿大社区健康调查中年龄≥60岁的安大略省居民的数据。我们估计了睡眠质量差的患病率(95%置信区间(CI))。我们调查了CBP与睡眠质量差之间的关系,以计算患病率(PR)和95% CI,控制协变量。我们通过四种组合暴露类别探讨了CBP和睡眠呼吸暂停之间的相互作用与睡眠质量差的关系。结果:总体而言,52%的参与者报告睡眠。结论:我们发现CBP与60岁以上安大略省居民的睡眠质量差有关。未来的研究应该调查CBP作为睡眠质量差的潜在危险因素。目的:研究“危险因素”(Les factors de risque d’un sommeil de mauvaise qualitest)的性质,并分析“危险因素”(Les factors de risque d’un sommeil de mauvaise qualitest)的性质。《年表问题》、《无效原因原理》、《质量问题》等。En premier lieu, nous avons danci.9cha.com, la pracimement de la mauvaise qualit du sommeil。第二个替代,而我们两者之间的问题我们l 'association dos chroniques et de la mauvaise质量sommeil然后得到带来了des ajustements倒tenir帐户des运用de covariables。最后,我们将探索“相互作用中心”和“交换交换中心”,以及“交换交换中心”和“交换交换中心”的问题,以及“交换交换中心”和“交换交换中心”的问题。msamothodes: Nous avons analysisles donnsamoes d' ontarienes et d'Ontariens de≥60和ayant participente . 'Enquête sur la santoresdans les collectivitcanalys canadiennes de 2015-2016。Nous avons estim la pracimvalence (intervalle de con未婚妻[IC] de 95%) de la mauvaise qualit du sommeil。我们已经我们两者之间PDC et l 'association la mauvaise质量sommeil倒计算des比率de患病率(RP) et des IC de 95%,然后得到带来了des ajustements倒tenir帐户des运用de covariables。Nous avons探索了l'interaction entre les PDC和l' apnsame du sommeil du point de vue de leur association和l' mauvaise qualites du sommeil de quatres de quatre cates和s ' expocomes。综上所述,有52%的人参与了该研究。结论:在所有的人群中,有15%的人参与了该研究。在所有的人群中,有15%的人参与了该研究。
{"title":"The association between chronic back problems and poor sleep quality among Ontarian adults aged 60 years and older: A cross-sectional study analyzing the Canadian Community Health Survey 2015-2016.","authors":"Pegah Rahbar, Jessica J Wong, Dan Wang, Efrosini Papaconstantinou, Sheilah Hogg-Johnson, Pierre Côté","doi":"10.17269/s41997-025-01123-4","DOIUrl":"https://doi.org/10.17269/s41997-025-01123-4","url":null,"abstract":"<p><strong>Objectives: </strong>Poor sleep quality's risk factors remain understudied in aging populations. Chronic back problems (CBP), a leading cause of disability, may contribute to poor sleep quality. Firstly, we determined the prevalence of poor sleep quality. Secondly, we investigated the association between chronic back problems and poor sleep quality, controlling for covariates. Lastly, we explored the interaction between sleep apnea and chronic back problems with respect to their association with poor sleep quality.</p><p><strong>Methods: </strong>We analyzed data from Ontarians ≥ 60 years in the 2015-2016 Canadian Community Health Survey. We estimated the prevalence (95% confidence interval (CI)) of poor sleep quality. We investigated the association between CBP and poor sleep quality to compute prevalence ratios (PR) and 95% CI, controlling for covariates. We explored the interaction between CBP and sleep apnea in their association with poor sleep quality using four combined exposure categories.</p><p><strong>Results: </strong>Overall, 52% of participants reported sleeping < 7 h or ≥ 9 h, 18% reported trouble going to/staying asleep, and 13% never/rarely felt refreshed. Controlling for covariates, CBP was associated with sleeping outside of recommended guidelines (PR = 1.19 (1.11-1.27)), trouble going to sleep or staying asleep (PR = 1.54 (1.32-1.79)), and rarely/never having refreshing sleep (PR = 1.45 (1.20-1.79)). No interaction was found between CBP and sleep apnea.</p><p><strong>Conclusion: </strong>We found that CBP is associated with poor sleep quality among Ontarians ≥ 60 years. Future studies should investigate CBP as a potential risk factor for poor sleep quality. Résumé Objectifs: Les facteurs de risque d'un sommeil de mauvaise qualité sont encore sous-étudiés dans les populations vieillissantes. Les problèmes de dos chroniques (PDC), l'une des principales causes d'invalidité, pourraient contribuer à la mauvaise qualité du sommeil. En premier lieu, nous avons déterminé la prévalence de la mauvaise qualité du sommeil. En deuxième lieu, nous avons étudié l'association entre les problèmes de dos chroniques et la mauvaise qualité du sommeil après avoir apporté des ajustements pour tenir compte des effets de covariables. Pour terminer, nous avons exploré l'interaction entre l'apnée du sommeil et les problèmes de dos chroniques du point de vue de leur association avec la mauvaise qualité du sommeil. Méthodes: Nous avons analysé les données d'Ontariennes et d'Ontariens de ≥ 60 ans ayant participé à l'Enquête sur la santé dans les collectivités canadiennes de 2015-2016. Nous avons estimé la prévalence (intervalle de confiance [IC] de 95%) de la mauvaise qualité du sommeil. Nous avons étudié l'association entre les PDC et la mauvaise qualité du sommeil pour calculer des ratios de prévalence (RP) et des IC de 95%, après avoir apporté des ajustements pour tenir compte des effets de covariables. Nous avons exploré l'interaction entre l","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145589670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-12DOI: 10.17269/s41997-025-01107-4
Jennifer E McWhirter, Melissa MacKay, Devon McAlpine, Lauren E Grant, Andrew Papadopoulos
Objective: Public health practice necessitates effective health communication. Now, more than ever, public health practitioners must possess the competencies - the skills, knowledge, and attitudes - to communicate effectively. Using a robust, multi-step, multi-method research process, we sought to develop a set of communication competency statements for public health professionals in Canada, in communication-focused roles.
Methods: Following earlier research steps that included scoping reviews, environmental scans, a national survey (n = 378), and key informant interviews (n = 12), which established an initial set of competency statements, a modified Delphi technique was conducted with a panel of public health communication experts which included two online survey rounds (n = 19, n = 18) with one virtual meeting (n = 7) in between to develop consensus on the initial competency statements. An a priori threshold for consensus of 75% agreement was set.
Results: After the second Delphi survey, participants reached consensus on all competency statements with 96% of participants agreeing with each statement on average, an increase from the first Delphi survey. Between the two Delphi surveys, revisions were made to the statements based on quantitative and qualitative participant feedback.
Conclusion: The research has resulted in 18 communication competency statements comprising the Public Health Communication Competency Framework, which are intended to serve as a roadmap for public health professionals whose roles encompass communication, guide curricula development in public health programs, catalyze professional development in communication, and support public health systems to achieve the essential public health functions.
{"title":"The Public Health Communication Competency Framework: Results from a multi-method and consensus-building process.","authors":"Jennifer E McWhirter, Melissa MacKay, Devon McAlpine, Lauren E Grant, Andrew Papadopoulos","doi":"10.17269/s41997-025-01107-4","DOIUrl":"https://doi.org/10.17269/s41997-025-01107-4","url":null,"abstract":"<p><strong>Objective: </strong>Public health practice necessitates effective health communication. Now, more than ever, public health practitioners must possess the competencies - the skills, knowledge, and attitudes - to communicate effectively. Using a robust, multi-step, multi-method research process, we sought to develop a set of communication competency statements for public health professionals in Canada, in communication-focused roles.</p><p><strong>Methods: </strong>Following earlier research steps that included scoping reviews, environmental scans, a national survey (n = 378), and key informant interviews (n = 12), which established an initial set of competency statements, a modified Delphi technique was conducted with a panel of public health communication experts which included two online survey rounds (n = 19, n = 18) with one virtual meeting (n = 7) in between to develop consensus on the initial competency statements. An a priori threshold for consensus of 75% agreement was set.</p><p><strong>Results: </strong>After the second Delphi survey, participants reached consensus on all competency statements with 96% of participants agreeing with each statement on average, an increase from the first Delphi survey. Between the two Delphi surveys, revisions were made to the statements based on quantitative and qualitative participant feedback.</p><p><strong>Conclusion: </strong>The research has resulted in 18 communication competency statements comprising the Public Health Communication Competency Framework, which are intended to serve as a roadmap for public health professionals whose roles encompass communication, guide curricula development in public health programs, catalyze professional development in communication, and support public health systems to achieve the essential public health functions.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145508051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-12DOI: 10.17269/s41997-025-01126-1
Marie-Claude Tremblay, Geneviève Olivier-D'Avignon, Sarah Sportès, Sandro Echaquan, Amanda Ottawa, Eniko Neashish, Taisha Niquay, Yvan-Rock Awashish, Christian Coocoo, Paul-Yves Weizineau
<p><strong>Objectives: </strong>This research is part of a larger participatory project aimed at co-developing an intervention to ensure cultural safety in care, conducted with and by the Atikamekw Nehirowisiwok (First Nation, Quebec Canada). A decolonizing research approach, integrating Atikamekw perspectives and ways of knowing, was adopted. The objectives of this phase of the project were to better understand the health care needs and perspectives of the Atikamekw peoples on cultural safety.</p><p><strong>Methods: </strong>Three talking circles were conducted from June 2022 to July 2022 in each of the three Atikamekw communities (Manawan, Wemotaci, and Opitciwan). Each talking circle comprised six to eight participants (a total of 21 participants) recruited on a voluntary basis. Talking circles lasted an average of 2 h and were conducted in French and Atikamekw. Data from talking circles were transcribed verbatim and analyzed using inductive thematic analysis by two members of the team. Collective interpretation of the results was informed by Atikamekw perspectives on the medicine wheel and the concept of Pimatisiwin.</p><p><strong>Results: </strong>The themes that emerged represent different Atikamekw needs regarding cultural safety in health care. These results highlight language accessibility, a welcoming approach, an anti-racist environment of care, the inclusion of traditional medicine and cultural perspectives, as well as self-determination as fundamental elements of culturally safe health care.</p><p><strong>Conclusion: </strong>This research project, carried out with and by the Atikamekw Nation, exemplifies how a decolonizing approach centered on the expertise of Indigenous communities can be used to develop culturally safe interventions that respect their needs, values, and cultural practices. Résumé Objectifs: Cette étude fait partie d'un projet participatif plus large visant à co-développer une intervention pour assurer la sécurité culturelle dans les soins, menée pour, par et avec les Atikamekw Nehirowisiwok (Première Nation, Québec, Canada). Une approche de recherche décolonisatrice, intégrant les perspectives et les modes de connaissance atikamekw, a été adoptée. Les objectifs de cette phase du projet étaient de mieux comprendre les besoins en matière de soins de santé et les points de vue des personnes Atikamekw sur la sécurité culturelle. Méthodes: Trois cercles de parole ont été organisés dans trois communautés atikamekw avec 6 à 8 participants (n = 21). Les cercles de parole ont duré en moyenne deux heures et se sont déroulés en français et en atikamekw. Les données des cercles de parole ont été transcrites et analysées par deux membres de l'équipe selon une approche thématique inductive. L'interprétation collective des résultats a été éclairée par les perspectives atikamekw de la roue de la médecine et le concept de Pimatisiwin. Résultats: Les résultats mettent en évidence l'importance de l'accessibilité linguistique, une ap
{"title":"Atikamekw needs and perspectives for culturally safe health care.","authors":"Marie-Claude Tremblay, Geneviève Olivier-D'Avignon, Sarah Sportès, Sandro Echaquan, Amanda Ottawa, Eniko Neashish, Taisha Niquay, Yvan-Rock Awashish, Christian Coocoo, Paul-Yves Weizineau","doi":"10.17269/s41997-025-01126-1","DOIUrl":"https://doi.org/10.17269/s41997-025-01126-1","url":null,"abstract":"<p><strong>Objectives: </strong>This research is part of a larger participatory project aimed at co-developing an intervention to ensure cultural safety in care, conducted with and by the Atikamekw Nehirowisiwok (First Nation, Quebec Canada). A decolonizing research approach, integrating Atikamekw perspectives and ways of knowing, was adopted. The objectives of this phase of the project were to better understand the health care needs and perspectives of the Atikamekw peoples on cultural safety.</p><p><strong>Methods: </strong>Three talking circles were conducted from June 2022 to July 2022 in each of the three Atikamekw communities (Manawan, Wemotaci, and Opitciwan). Each talking circle comprised six to eight participants (a total of 21 participants) recruited on a voluntary basis. Talking circles lasted an average of 2 h and were conducted in French and Atikamekw. Data from talking circles were transcribed verbatim and analyzed using inductive thematic analysis by two members of the team. Collective interpretation of the results was informed by Atikamekw perspectives on the medicine wheel and the concept of Pimatisiwin.</p><p><strong>Results: </strong>The themes that emerged represent different Atikamekw needs regarding cultural safety in health care. These results highlight language accessibility, a welcoming approach, an anti-racist environment of care, the inclusion of traditional medicine and cultural perspectives, as well as self-determination as fundamental elements of culturally safe health care.</p><p><strong>Conclusion: </strong>This research project, carried out with and by the Atikamekw Nation, exemplifies how a decolonizing approach centered on the expertise of Indigenous communities can be used to develop culturally safe interventions that respect their needs, values, and cultural practices. Résumé Objectifs: Cette étude fait partie d'un projet participatif plus large visant à co-développer une intervention pour assurer la sécurité culturelle dans les soins, menée pour, par et avec les Atikamekw Nehirowisiwok (Première Nation, Québec, Canada). Une approche de recherche décolonisatrice, intégrant les perspectives et les modes de connaissance atikamekw, a été adoptée. Les objectifs de cette phase du projet étaient de mieux comprendre les besoins en matière de soins de santé et les points de vue des personnes Atikamekw sur la sécurité culturelle. Méthodes: Trois cercles de parole ont été organisés dans trois communautés atikamekw avec 6 à 8 participants (n = 21). Les cercles de parole ont duré en moyenne deux heures et se sont déroulés en français et en atikamekw. Les données des cercles de parole ont été transcrites et analysées par deux membres de l'équipe selon une approche thématique inductive. L'interprétation collective des résultats a été éclairée par les perspectives atikamekw de la roue de la médecine et le concept de Pimatisiwin. Résultats: Les résultats mettent en évidence l'importance de l'accessibilité linguistique, une ap","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145497389","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-10DOI: 10.17269/s41997-025-01128-z
Yuan Yu, Jiacheng Chen, Matthew J Knight, Sheila F O'Brien, David L Buckeridge, Carmen L Charlton, W Alton Russell
Objective: SARS-CoV-2 serological surveillance used blood donors, research cohorts, and residual patient samples. Differences in socio-demographic characteristics across these sources may bias seroprevalence estimates, necessitating statistical adjustment.
Methods: We re-analyzed data from six serosurveillance sources, comparing the estimated percent of the population positive for SARS-CoV-2 anti-nucleocapsid antibodies for six regions during periods when the sources' sample collection overlapped. We assessed the concordance between sources with and without using multilevel regression and poststratification (MRP) to adjust for differences in representation by age, sex, and race.
Results: Across regions and timepoints, unadjusted seroprevalence differed between sources by up to 20%. MRP did not consistently improve comparability of seroprevalence across sources. In 2022, seroprevalence was consistently highest among blood donors, and MRP increased regional seroprevalence across all sources (except in Manitoba during January-April 2022 in ABC Study). In a secondary regression analysis, immunoassay kit and sample type (dried blood spot or venous blood draw) strongly influenced the odds that a sample was classified as seropositive.
Conclusion: Adjusting for representativeness using common socio-demographic variables did not systematically improve concordance in seropositivity estimates between serosurveillance sources. While discrepancies between sources might be influenced by studies' representativeness of characteristics we did not assess, methods for measuring seropositivity appear to explain much of the differences between sources. Serosurveillance findings are influenced by many aspects of study design beyond representativeness, such as sample type (venous blood draw or dried blood spots), choice of immunoassay, and laboratory procedures such as dilution or immunoassay calibration.
{"title":"Comparability of Canadian SARS-CoV-2 seroprevalence estimates with statistical adjustment for socio-demographic representation.","authors":"Yuan Yu, Jiacheng Chen, Matthew J Knight, Sheila F O'Brien, David L Buckeridge, Carmen L Charlton, W Alton Russell","doi":"10.17269/s41997-025-01128-z","DOIUrl":"https://doi.org/10.17269/s41997-025-01128-z","url":null,"abstract":"<p><strong>Objective: </strong>SARS-CoV-2 serological surveillance used blood donors, research cohorts, and residual patient samples. Differences in socio-demographic characteristics across these sources may bias seroprevalence estimates, necessitating statistical adjustment.</p><p><strong>Methods: </strong>We re-analyzed data from six serosurveillance sources, comparing the estimated percent of the population positive for SARS-CoV-2 anti-nucleocapsid antibodies for six regions during periods when the sources' sample collection overlapped. We assessed the concordance between sources with and without using multilevel regression and poststratification (MRP) to adjust for differences in representation by age, sex, and race.</p><p><strong>Results: </strong>Across regions and timepoints, unadjusted seroprevalence differed between sources by up to 20%. MRP did not consistently improve comparability of seroprevalence across sources. In 2022, seroprevalence was consistently highest among blood donors, and MRP increased regional seroprevalence across all sources (except in Manitoba during January-April 2022 in ABC Study). In a secondary regression analysis, immunoassay kit and sample type (dried blood spot or venous blood draw) strongly influenced the odds that a sample was classified as seropositive.</p><p><strong>Conclusion: </strong>Adjusting for representativeness using common socio-demographic variables did not systematically improve concordance in seropositivity estimates between serosurveillance sources. While discrepancies between sources might be influenced by studies' representativeness of characteristics we did not assess, methods for measuring seropositivity appear to explain much of the differences between sources. Serosurveillance findings are influenced by many aspects of study design beyond representativeness, such as sample type (venous blood draw or dried blood spots), choice of immunoassay, and laboratory procedures such as dilution or immunoassay calibration.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145490901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-06DOI: 10.17269/s41997-025-01091-9
Sonja Wicklum, Tia Black, Loretta Tuttauk, Lynden Lindsay Crowshoe, Yunqi Jacob Ji, Kerry McBrien, Jessica Zhang, Carly Checholik, Ashley Amson, Patricia Doyle-Baker, Alicia Oliver, Levi Frehlich
Objectives: This environmental scan has two aims. The first is to identify wholistic, physical activity (PA)-based wellness interventions for Indigenous women in Canada through the completion of a scoping review of published and grey literature and key informant interviews. The second is to identify promising practices and potential barriers to intervention development and delivery.
Methods: Components of the environmental scan included (1) the creation of a logic model in collaboration with a community-based Advisory Group, (2) a scoping review of wholistic PA-based wellness interventions between January 1990 and March 2022, (3) key informant interviews of individuals involved in PA-based wellness programming, and (4) thematic analysis of promising practices, enablers, and barriers found in both the articles and interviews.
Synthesis: The scoping review identified 16 interventions. Through key informant interviews, 6 additional interventions were identified. Programs were largely community-based and culturally appropriate. Financial factors were the most common barrier. Walking as a form of PA was commonly employed and key informant interviews highlighted the importance of exploring on-the-land activities, group activities, and the incorporation of all elements of wholistic health (mental, physical, spiritual, and emotional). Only one study employed Indigenous research methods.
Conclusion: There is limited published literature and a dearth of PA-based, wholistic health programs for Indigenous women in Canada. More programming and research are required to address the unique health needs of Indigenous women and mitigate the legacy impacts of colonization on health.
{"title":"Physical activity-based, wholistic, wellness interventions for Indigenous women in Canada: An environmental scan to identify programs and promising practices.","authors":"Sonja Wicklum, Tia Black, Loretta Tuttauk, Lynden Lindsay Crowshoe, Yunqi Jacob Ji, Kerry McBrien, Jessica Zhang, Carly Checholik, Ashley Amson, Patricia Doyle-Baker, Alicia Oliver, Levi Frehlich","doi":"10.17269/s41997-025-01091-9","DOIUrl":"https://doi.org/10.17269/s41997-025-01091-9","url":null,"abstract":"<p><strong>Objectives: </strong>This environmental scan has two aims. The first is to identify wholistic, physical activity (PA)-based wellness interventions for Indigenous women in Canada through the completion of a scoping review of published and grey literature and key informant interviews. The second is to identify promising practices and potential barriers to intervention development and delivery.</p><p><strong>Methods: </strong>Components of the environmental scan included (1) the creation of a logic model in collaboration with a community-based Advisory Group, (2) a scoping review of wholistic PA-based wellness interventions between January 1990 and March 2022, (3) key informant interviews of individuals involved in PA-based wellness programming, and (4) thematic analysis of promising practices, enablers, and barriers found in both the articles and interviews.</p><p><strong>Synthesis: </strong>The scoping review identified 16 interventions. Through key informant interviews, 6 additional interventions were identified. Programs were largely community-based and culturally appropriate. Financial factors were the most common barrier. Walking as a form of PA was commonly employed and key informant interviews highlighted the importance of exploring on-the-land activities, group activities, and the incorporation of all elements of wholistic health (mental, physical, spiritual, and emotional). Only one study employed Indigenous research methods.</p><p><strong>Conclusion: </strong>There is limited published literature and a dearth of PA-based, wholistic health programs for Indigenous women in Canada. More programming and research are required to address the unique health needs of Indigenous women and mitigate the legacy impacts of colonization on health.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145460596","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: This qualitative study examines how trust has changed during and after the pandemic among our study participants. It reveals how they made meaning of trust in federal and provincial governments, scientific research, and digital platforms, and how this meaning-making process changed and was challenged by a global public health crisis.
Methods: We applied a descriptive phenomenological approach to semi-structured interviews that were conducted between July and November of 2024. In total, 41 interviews were conducted. Interview transcripts were analyzed using the descriptive phenomenological approach to understand participants' lived experiences of the pandemic, followed by how these lived experiences contributed to how they made meaning of public trust, both during and after the height of the pandemic. This analysis resulted in themes by giving attention to expressive language and past experiences, and ultimately revealing the "essence" or distinct nature of these participants' experiences of the pandemic.
Results: Research participants expressed polarized views on government trust, with provincial administrations often perceived as prioritizing economic or political interests over public health, while federal government were associated more with incompetence than with self-serving motives. Our participants experienced relatively stable trust in scientists, though they were concerned about transparency and profit-driven motives - particularly concerning the short time it took for vaccines to be developed. Social media was largely perceived as an unreliable source of information, yet it remained influential in shaping participants' perceptions, especially regarding vaccine hesitancy.
Conclusions: We found that participants' public trust during the pandemic in Canada was highly dynamic and subjective, and was greatly informed by histories, lived experiences, and preconceptions about various institutions, such as the government, public health officials, and scientists. Changes in trust experienced by participants were anchored in experts' ability to communicate reliable information. Participants further emphasized the need for transparent and consistent messaging, particularly from the Government of Canada, to rebuild lost trust and prepare for future public health crises.
{"title":"\"Just be honest with us\": A qualitative analysis of Canadians' public trust during the COVID-19 pandemic.","authors":"Nazeem Muhajarine, Cory Neudorf, Fionnuala Braun, Khatira Mehdiyeva, Katrina Baudelaire, Abang Omot, Bobbi Bedard, Kevin Entwistle, Thilina Bandara, Sohana Sadique, Ninan Abraham, Kimberly Huyser, Kim L Lavoie, Ève Dubé, Claire Betker","doi":"10.17269/s41997-025-01121-6","DOIUrl":"https://doi.org/10.17269/s41997-025-01121-6","url":null,"abstract":"<p><strong>Objectives: </strong>This qualitative study examines how trust has changed during and after the pandemic among our study participants. It reveals how they made meaning of trust in federal and provincial governments, scientific research, and digital platforms, and how this meaning-making process changed and was challenged by a global public health crisis.</p><p><strong>Methods: </strong>We applied a descriptive phenomenological approach to semi-structured interviews that were conducted between July and November of 2024. In total, 41 interviews were conducted. Interview transcripts were analyzed using the descriptive phenomenological approach to understand participants' lived experiences of the pandemic, followed by how these lived experiences contributed to how they made meaning of public trust, both during and after the height of the pandemic. This analysis resulted in themes by giving attention to expressive language and past experiences, and ultimately revealing the \"essence\" or distinct nature of these participants' experiences of the pandemic.</p><p><strong>Results: </strong>Research participants expressed polarized views on government trust, with provincial administrations often perceived as prioritizing economic or political interests over public health, while federal government were associated more with incompetence than with self-serving motives. Our participants experienced relatively stable trust in scientists, though they were concerned about transparency and profit-driven motives - particularly concerning the short time it took for vaccines to be developed. Social media was largely perceived as an unreliable source of information, yet it remained influential in shaping participants' perceptions, especially regarding vaccine hesitancy.</p><p><strong>Conclusions: </strong>We found that participants' public trust during the pandemic in Canada was highly dynamic and subjective, and was greatly informed by histories, lived experiences, and preconceptions about various institutions, such as the government, public health officials, and scientists. Changes in trust experienced by participants were anchored in experts' ability to communicate reliable information. Participants further emphasized the need for transparent and consistent messaging, particularly from the Government of Canada, to rebuild lost trust and prepare for future public health crises.</p>","PeriodicalId":51407,"journal":{"name":"Canadian Journal of Public Health-Revue Canadienne De Sante Publique","volume":" ","pages":""},"PeriodicalIF":2.6,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145446284","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}