Relevant bibliographies by topics / Health advocacy

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Health advocacy'

Author: Grafiati
Published: 4 June 2021
Last updated: 4 February 2022

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Journal articles on the topic "Health advocacy"

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Hubinette, Maria, Sarah Dobson, Ian Scott, and Jonathan Sherbino. "Health advocacy." Medical Teacher 39, no. 2 (November 21, 2016): 128–35. http://dx.doi.org/10.1080/0142159x.2017.1245853.

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Berman, Micah L., Elizabeth Tobin-Tyler, and Wendy E. Parmet. "The Role of Advocacy in Public Health Law." Journal of Law, Medicine & Ethics 47, S2 (2019): 15–18. http://dx.doi.org/10.1177/1073110519857308.

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This article discusses how advocacy can be taught to both law and public health students, as well as the role that public health law faculty can play in advocating for public health. Despite the central role that advocacy plans in translating public health research into law, policy advocacy skills are rarely explicitly taught in either law schools or schools of public health, leaving those engaged in public health practice unclear about whether and how to advocate for effective policies. The article explains how courses in public health law and health justice provide ideal opportunities to teach advocacy skills, and it discusses the work of the George Consortium, which seeks to engage public health law faculty in advocacy efforts.
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Ridley, Julie, Karen Newbigging, and Cathy Street. "Mental health advocacy outcomes from service user perspectives." Mental Health Review Journal 23, no. 4 (December 10, 2018): 280–92. http://dx.doi.org/10.1108/mhrj-10-2017-0049.

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Purpose The purpose of this paper is to address a knowledge gap on advocacy outcomes from mental health service users’ perspective, and the implications for evaluating advocacy impact. The studies discussed highlight challenges for measuring the outcomes of advocacy, but underline the importance of doing so, and of involving service users alongside other stakeholders in co-designing evaluation systems. Design/methodology/approach The paper uses findings from three qualitative studies of independent advocacy involving focus groups and interviews with: 30 African and African Caribbean men who were mental health service users; 90 “qualifying patients” in a study of Independent Mental Health Advocate services; and nine young women in children and adolescent mental health services (CAMHS). Findings A comparative analysis and synthesis of findings from three studies identifies four common dimensions: how mental health advocacy is conceptualised and understood; how service users define advocacy outcomes; wider impacts; and, user involvement in evaluating advocacy outcomes. Advocacy outcomes were conceptualised as increasing involvement, changing care and treatment and supporting personal development. There was evidence of advocacy acting to empower mental health service users, and of broader impacts on service regimes and policies. However, there was limited evidence of transformational impact. Evaluating advocacy outcomes is increasingly seen as important. Originality/value Few researchers have focused primarily on the perspectives of people using independent mental health advocacy, or on the experience of “advocacy as empowerment”, and none have done so across diverse groups. This analysis adds insight into the impact of independent advocacy. Data from empirical studies attest to the important role independent advocacy plays in modern mental health systems.
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Bassett, Mary T. "Public Health Advocacy." American Journal of Public Health 93, no. 8 (August 2003): 1204. http://dx.doi.org/10.2105/ajph.93.8.1204.

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Santoro, Maya S., Dhwani J. Kothari, Charles Van Liew, and Terry A. Cronan. "Health Care Advocacy." Californian Journal of Health Promotion 12, no. 3 (December 1, 2014): 46–55. http://dx.doi.org/10.32398/cjhp.v12i3.1580.

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Background and Purpose: The U.S. population is living longer; therefore, a relatively large proportion of the population is likely to experience chronic illnesses within their lifetime. An experimental study was conducted to examine factors influencing the likelihood of hiring a Health Care Advocate (HCA). Methods: Survey data were collected from a randomly selected community sample of participants (N = 470) over the age of 18 who were provided with a description of an HCA and a written vignette describing a medical scenario. Participants read one of eight vignettes in which they were asked to imagine they were in a car accident and required medical care. Age, injury (chronic vs. acute), and presence of comorbid chronic condition were manipulated. Results: A significant interaction indicated that when there was no pre-existing chronic health condition, sustaining a chronic injury increased the likelihood of hiring an HCA. In addition, younger adults with comorbid conditions were perceived as having greater need for an HCA than younger adults without comorbid conditions. Older adults were perceived as benefiting from HCAs regardless of comorbid conditions. Conclusion: This study demonstrates the need for patient-centered support for older adults following an injury, and for younger adults when a pre-existing chronic condition exists. Efforts should be made to target services to these populations of interest.
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Acheson, Donald, and Graham Hart. "Public health advocacy." Lancet 345, no. 8956 (April 1995): 1050. http://dx.doi.org/10.1016/s0140-6736(95)90789-0.

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Baffour, Tiffany D., Maurine A. Jones, and Linda K. Contreras. "Family Health Advocacy." Family & Community Health 29, no. 3 (July 2006): 221–28. http://dx.doi.org/10.1097/00003727-200607000-00009.

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Loue, S. "Community health advocacy." Journal of Epidemiology & Community Health 60, no. 6 (June 1, 2006): 458–63. http://dx.doi.org/10.1136/jech.2004.023044.

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Gil, D. "Community health advocacy." Journal of Epidemiology & Community Health 58, no. 1 (January 1, 2004): 79. http://dx.doi.org/10.1136/jech.58.1.79.

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Leveridge, Michael, Darren Beiko, James W. L. Wilson, and Robert Siemens. "Health advocacy training in urology: a Canadian survey on." Canadian Urological Association Journal 1, no. 4 (March 4, 2013): 363. http://dx.doi.org/10.5489/cuaj.438.

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Introduction: Health advocacy is a well-defined core competency recognizedby medical education and regulatory bodies. Advocacy is stressed as a criticalcomponent of a physician’s function within his or her community andalso of performance evaluation during residency training. We sought to assessurology residents’ perceptions and attitudes toward health advocacy in residencytraining and practice.Methods: We administered an anonymous, cross-sectional, self-report questionnaireto all final-year urology residents in Canadian training programs. The surveywas closed-ended and employed a 5-point Likert scale. It was designedto assess familiarity with the concept of health advocacy and with its applicationand importance to training and practice. We used descriptive and correlativestatistics to analyze the responses, such as the availability of formaltraining and resident participation in activities involving health advocacy.Results: There was a 93% response rate among the chief residents. Most residentswere well aware of the role of the health advocate in urology, and a majority(68%) believed it is important in residency training and in the urologist’s rolein practice. This is in stark contrast to acknowledged participation and formaltraining in health advocacy. A minority (7%–25%) agreed that formal trainingor mentorship in health advocacy was available at their institution, and only21%–39% felt that they had used its principles in the clinic or community. Only4%–7% of residents surveyed were aware of or had participated in local urologicalhealth advocacy groups.Conclusion: Despite knowledge about and acceptance of the importance ofthe health advocate role, there is a perceived lack of formal training and a dearthof participation during urological residency training.
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Dissertations / Theses on the topic "Health advocacy"

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Decker, Karen M. "A study of relationships between counselor education, social justice advocacy competence, and likelihood to advocate." Thesis, Capella University, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3602466.

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The relationship between social justice advocacy training, counselor competence in social justice advocacy and likelihood to advocate of counselor educators and counselor trainees who are in the practicum and internship phase of their training in Council for the Accreditation of Counseling and Related Educational Programs (CACREP)-accredited master's-level counselor education programs has not been researched. Developing an empirical understanding of these relationships is needed to inform counselor education practices related to preparation for social justice advocacy. The purpose of this study was to take a preliminary step toward filling the gap in current literature concerning counselor education and its role in preparing counselors to be social justice advocates. A convenience sample of 112 counselor educators and counselor trainees who are in the practicum and internship phase of their training in CACREP-accredited master's-level counselor education programs was utilized. The specific research design was a correlational survey research design utilizing multivariate linear regression analysis and correlational analysis using SPSS that examined the relationship between the variables of social justice advocacy training, ratings of competence in social justice advocacy, and the likelihood to advocate. It also examined the relationship in ratings of competence in social justice advocacy and the likelihood to advocate between counselor educators and counselor trainees. The findings indicate that there is a significant relationship between social justice advocacy training and ratings of social justice advocacy competence. It also appears that advocacy training leads to an increased likelihood to advocate particularly at community and societal levels. The findings further indicate that counselor trainees who report greater advocacy competence are more likely to engage in advocacy activities at the three levels of advocacy as defined by the ACA Advocacy Competencies (ACA, 2003). These findings taken together support the inclusion of social justice advocacy training in counselor education programs.

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Frame, Laura N. "Georgia Environmental Advocacy Groups Health Education Needs Assessment." Digital Archive @ GSU, 2012. http://digitalarchive.gsu.edu/iph_theses/218.

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Georgia State University’s Institute of Public Health along with the Georgia Department of Public Health’s Chemical Hazards Program conducted a needs assessment survey to learn more about the concerns of environmental advocates and other community leaders in Georgia regarding exposure to toxic chemicals. The purpose of the Georgia Environmental Advocacy Groups Health Education Needs Assessment was to better understand community concerns, to identify hazardous waste sites that might warrant some degree of public health evaluation, to find community leaders and personnel interested in assisting the Chemical Hazards Program in implementing public health interventions, to inform the community about the services offered to the public by the Georgia Department of Public Health and to better understand the best methods for distributing health education material. This is the first time the Chemical Hazards Program has conducted an environmental advocacy group leader needs assessment. The results of this pilot study will help the development of future needs assessments conducted by the CHP. Survey development began in August of 2011 and Georgia State University Institutional Review Board approval was granted January 2012. Participants were selected due to their current leadership role of a Georgia environmental advocacy group/organization. Contact information was found for 137 environmental group leaders. Depending on available contact information, potential participants either received the survey through the mail or electronically via email. Surveys were distributed on January 13, 2012 and had to be returned by February 20, 2012. Twenty-one Georgia environmental advocacy group leaders participated in the survey. A majority of participants cited protect/restore natural habitats as the main purpose of their organization, but the survey did reveal 10 environmental groups that focused on protecting human health. Seven of participants that were dedicated to protecting human health expressed interest in working further with the GDPH to develop or implement public health interventions. The survey was also successful in informing participants about the Chemical Hazards Program. Prior to the needs assessment, more than 80% of participants were not aware of the program. Many pertinent suggestions were also made to aid in the development of the brochure aimed at educating community members about the services offered by the CHP. Although a variety of environmental health concerns were cited by the participants, water quality was most often mentioned. More participants reported they were very concerned about drinking water than any other environment. Ninety percent also reported being either concerned or very concerned about contamination in oceans, lakes and streams. A section of the survey also addressed hazards found within the home, unclean drinking water was selected by far the most often as being of greatest concern compared to all other indoor hazards. Many participants listed specific waste or industrial sites that are of concern among members of their community as a source of contaminants. A few contaminated environments were also listed including specific rivers and lakes. Though many did not list specific sources, the majority of participants cited water contamination as being a chemical contamination issue that has the greatest impact on human health. The survey helped reveal specific community concerns regarding potential chemical contaminants and sites that may lead to the CHP conducting public health assessments/consultations and exposure investigations. The survey also revealed the need for general environmental health education and intervention activities based on concerns of the participants as well as the lack of concern by many. The survey was also successful in identifying individuals that may help the CHP gain future partnerships and identifying creative methods for distributing health education material. The CHP plans to follow-up with many of the participants and the survey will be further developed and used to survey other leaders, community members, and public health workers etc. to further investigate the needs and concerns of communities across Georgia.
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Richards, Anika Tahirah. "Health Equity Education, Awareness, and Advocacy through the Virginia Department of Health Health Equity Campaign." Diss., Virginia Tech, 2011. http://hdl.handle.net/10919/77312.

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This study showed that health equity must be achieved through education, awareness, and advocacy. A structured program must be put in place to provide accountability towards achieving health equity within organizations, communities, cites, and states. In Virginia, the Health Equity Campaign was a program put in place to provide such accountability to the citizens of Virginia. This study attempted to evaluate the Health Equity Campaign implemented by the Virginia Department of Health Office of Minority Health and Public Health Policy Division of Health Equity in order to get all Virginians to become advocates for health equity in their organizations, communities, neighborhoods. Organizational/group leaders were interviewed in addition to surveying various staff members. This study provides a detailed description of the strength of the Health Equity Campaign's ability to promote education and awareness about health equity and why many participants found it difficult to transition from motivation to advocacy.
Ph. D.
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Schetzina, Karen E. "Breastfeeding Advocacy Benefits Everyone (BABE) Coalition." Digital Commons @ East Tennessee State University, 2011. https://dc.etsu.edu/etsu-works/5125.

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Mitten, Lauren. "Phthalates: Science, Advocacy, and Biomonitoring." Scholarship @ Claremont, 2015. http://scholarship.claremont.edu/scripps_theses/614.

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Phthalates are a class of ubiquitous environmental contaminants that cause health problems including reproductive disorders, asthma, and obesity. Advocacy against phthalates has been taking place in the US since the mid-1990s, and eight in-depth interviews were conducted with advocates and scientists in order to construct a history of this advocacy. There have been a variety of campaigns and victories; those around medical devices, children’s products, and personal care products are examined in detail. Phthalate exposure data for a representative sample of the US population indicates that exposure to DEP, DEHP, DnBP, and BBzP went down between 1999 and 2010. As these were the phthalates that had the largest volume of advocacy during the period researched, this decrease suggests that advocacy around specific phthalates is effective in reducing exposure and that more advocacy around phthalates, and potentially other harmful chemicals, could result in further decreased exposure and improved health in the US population. Additional research using more finely graded biomonitoring data would help deepen understanding about correlations between advocacy and phthalate exposure. In reviewing the health effects of phthalates, it was found that a disproportionate amount of the research is on male reproductive health effects, which is partially responsible for the fact that a disproportionate amount of phthalate advocacy is on heath effects relating to men, particularly male babies. Both phthalate science and advocacy sometimes treat women instrumentally, objectifying them or regarding them as incubators. To combat this, scientists could do more research on the health effects of phthalates on women and advocates could take more care not to neglect or instrumentalize women in their efforts to reduce phthalate exposure for all people.
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Nicholson-Crotty, Jill Denise. "The stages of nonprofit advocacy." Texas A&M University, 2005. http://hdl.handle.net/1969.1/4956.

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This dissertation argues that advocacy is a two-stage decision in which organizations must first decide whether or not to undertake political activity through advocacy or lobbying and then choose between the set of strategic actions that, based on available financial and human resources, are available to them. These are separate decisions with separate constraints. The decision to advocate is a strategic stance taken by nonprofit organizations in policy environments that necessitate such activity and in which it is politically conducive for them to undertake the cost of such actions. Once an organization has decided that it will undertake advocacy activities, it must determine the specific activities, collaboration, grassroots advocacy, or direct lobbying, that will help it to pursue that course most effectively. These hypotheses are tested in an analysis of the advocacy activities of over 500 nonprofit reproductive health service providers. Data for this study were gathered from the National Center for Charitable Statistics within the Urban Institute and directly from IRS Form 990s filed by the organizations. The findings suggest that there are strong and consistent relationships between policy and politics and the political activity of nonprofit service providers. In states with more restrictive reproductive health policy environments, nonprofit organizations that provide these services are more likely to engage in advocacy activity. The findings also suggest that, even when controlling for the policy environment, 501(c)(3)s are more likely to become politically active in states where they have a larger number of political allies. Additional analyses suggest that there is a negative relationship between government monies and the aggressiveness of advocacy and the use of multiple advocacy strategies. Interestingly, this finding is consistent with the expectations offered in the resource dependence literature and the results suggest only a tenuous relationship between institutional variables and decisions regarding organizational aggressiveness in the choice of advocacy strategies.
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Garcia, Patricia B. "Public Health in Georgia, An Internet Advocacy Tool: A Capstone Project." Digital Archive @ GSU, 2010. http://digitalarchive.gsu.edu/iph_theses/131.

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Local Public Health programs are at the frontline of Georgia’s struggle to prevent disease, prolong citizens’ lives, and promote health. In recent history it has been observed that both Georgia’s citizens and state government do not completely understand the breadth of the Public Health system and all it beneficiaries. Unfortunately this lack of comprehension about the scope of Public Health programs has lead to a significant decrease in support and funding. This capstone project describes the systematic development of an online educational portal that is a central tool used in the Public Health advocacy campaign in Georgia, “Partner-Up for Public Health”. An electronic database of Public Health statistics for all of Georgia’s counties (n=159) was created using secondary sources. The database presents data on four primary domains: geographic/population descriptive statistics, broad social determinants of health, health indicators, and health outcomes. Within these domains, there are a total of twenty-one indices. This project is important because it collects and presents Public Health information into one centralized location for easy retrieval and is formatted to deliver content in non-technical jargon. A hallmark of the online portal is that it facilitates the mobilization of information and tools necessary for Georgian’s to advocate for local Public Health action, programs, funding, and political attention.
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Wu, Fengshi. "Double-mobilization transnational advocacy networks for China's environment and public health /." College Park, Md. : University of Maryland, 2005. http://hdl.handle.net/1903/2970.

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Thesis (Ph. D.) -- University of Maryland, College Park, 2005.
Thesis research directed by: Government and Politics. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
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Luschen, Kristen V. "Empowering prevention? adolescent female sexuality, advocacy and schooling /." Related electronic resource: Current Research at SU : database of SU dissertations, recent titles available full text, 2005. http://wwwlib.umi.com/cr/syr/main.

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Squires, Erika S. "Education and Advocacy for Individuals with Hearing Loss." University of Toledo / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1470162746.

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Books on the topic "Health advocacy"

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White-Farnham, Jamie, Bryna Siegel Finer, and Cathryn Molloy, eds. Women’s Health Advocacy. First edition. | New York, NY : Routledge, 2019.: Routledge, 2019. http://dx.doi.org/10.4324/9780429201165.

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Loue, Sana. Community health advocacy. New York: Kluwer Academic/Plenum Publishers, 2003.

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Sessums, Laura, Lyle Dennis, Mark Liebow, William Moran, and Eugene Rich, eds. Health Care Advocacy. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6914-9.

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Michelle, Funk, Saraceno Benedetto, Minoletti Alberto, and World Health Organization, eds. Advocacy for mental health. Geneva: World Health Organization, 2003.

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Marks, Joan H., ed. Advocacy in Health Care. Totowa, NJ: Humana Press, 1986. http://dx.doi.org/10.1007/978-1-4612-5004-3.

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Chanyasulkit, Chris. Successful Public Health Advocacy. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-30288-7.

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University of East Anglia. School of Social Work., ed. Advocacy and mental health. Norwich: School of Social Work, University of East Anglia, 2000.

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Advocacy in health care. Osney Mead, Oxford, OX: Blackwell Science, 1998.

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Community health nursing: Advocacy for population health. 5th ed. Upper Saddle River, N.J: Pearson Prentice Hall, 2008.

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Advocacy strategies for health and mental health professionals: From patients to policies. New York: Springer, 2012.

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Book chapters on the topic "Health advocacy"

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Laverack, Glenn. "Advocacy." In A–Z of Health Promotion, 1–3. London: Macmillan Education UK, 2014. http://dx.doi.org/10.1007/978-1-137-35049-7_1.

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Laverack, Glenn. "Advocacy." In A–Z of Public Health, 8–10. London: Macmillan Education UK, 2015. http://dx.doi.org/10.1007/978-1-137-42617-8_4.

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Rysdam, Sheri. "Doula Advocacy." In Women’s Health Advocacy, 90–101. First edition. | New York, NY : Routledge, 2019.: Routledge, 2019. http://dx.doi.org/10.4324/9780429201165-12.

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Heinrich, Max. "Mental health advocacy." In Reflections of a Cynical Clinical Psychologist, 123–28. Abingdon, Oxon ; New York, NY : Routledge, 2020.: Routledge, 2020. http://dx.doi.org/10.4324/9780429320965-21.

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Ravich, Ruth. "Patient Advocacy." In Advocacy in Health Care, 51–60. Totowa, NJ: Humana Press, 1986. http://dx.doi.org/10.1007/978-1-4612-5004-3_6.

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Liebow, Mark, and Tina Liebling. "State-Level Advocacy." In Health Care Advocacy, 93–99. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6914-9_9.

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Patel, Kavita K., Harry P. Selker, and Harry P. Selker. "Building Partnerships and Coalition Advocacy." In Health Care Advocacy, 79–91. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6914-9_8.

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Rich, Eugene C. "Clinicians and Health Care Advocacy: The Reasons Why." In Health Care Advocacy, 1–12. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6914-9_1.

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Carr, Michael B., Barbara Waters Roop, and John D. Goodson. "Local Advocacy for the Health Care Professional." In Health Care Advocacy, 101–12. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6914-9_10.

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Rich, Eugene C., Laura L. Sessums, Lyle B. Dennis, William P. Moran, and Mark Liebow. "Clinicians and Health Care Advocacy: What Comes Next?" In Health Care Advocacy, 113–24. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6914-9_11.

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Conference papers on the topic "Health advocacy"

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Nathaniel, Diane. "Abstract C117: [Advocate Abstract] Saving lives through advocacy." In Abstracts: Eleventh AACR Conference on The Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; November 2-5, 2018; New Orleans, LA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7755.disp18-c117.

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Kasman, Kasman, Darmawansyah Darmawansyah, Alimin Maidin, and Amran Razak. "Advocacy of Increasing Health Budget in The Parepare City." In Proceedings of the 3rd International Conference on Environmental Risks and Public Health, ICER-PH 2018, 26-27, October 2018, Makassar, Indonesia. EAI, 2019. http://dx.doi.org/10.4108/eai.26-10-2018.2288698.

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Dornan, Wayne. "Abstract A87: [Advocate Abstract:] Bridging the Gap Between Science and Patient Advocacy." In Abstracts: Ninth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; September 25-28, 2016; Fort Lauderdale, FL. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7755.disp16-a87.

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Nix, Melanie A. "Abstract A60: My advocacy ecosystem." In Abstracts: Seventh AACR Conference on The Science of Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; November 9-12, 2014; San Antonio, TX. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7755.disp14-a60.

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Goodwin, Jean. "What is “Responsible Advocacy” in Science? Good Advice." In 2016: Confronting the challenges of public participation in environmental, planning and health decision-making. Iowa State University, Digital Press, 2012. http://dx.doi.org/10.31274/sciencecommunication-180809-65.

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Currie, Jacqueline Waldine. "Abstract C96: Community education; community advocacy." In Abstracts: Eighth AACR Conference on The Science of Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; November 13-16, 2015; Atlanta, Georgia. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7755.disp15-c96.

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Burry, Yvonne H. "Abstract B46: Advocacy for breast cancer and for community health initiatives." In Abstracts: Seventh AACR Conference on The Science of Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; November 9-12, 2014; San Antonio, TX. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7755.disp14-b46.

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Saniatuzzulfa, Rahmah, Rini Setyowati, and Rohmaningtyas Hidayah Setyaningrum. "Health Cadre Advocacy for Early Detection of Psychological Disorder in the Elderly." In The 5th Intenational Conference on Public Health 2019. Masters Program in Public Health, Universitas Sebelas Maret, 2019. http://dx.doi.org/10.26911/theicph.2019.02.05.

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Pahl, NJ. "1596 Advocacy training to achieve positive national policy change in occupational health." In 32nd Triennial Congress of the International Commission on Occupational Health (ICOH), Dublin, Ireland, 29th April to 4th May 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/oemed-2018-icohabstracts.187.

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Cortes, RN. "P6.02 A regional advocacy agenda on transgender health and sexual health among transgender people in the isean region." In STI and HIV World Congress Abstracts, July 9–12 2017, Rio de Janeiro, Brazil. BMJ Publishing Group Ltd, 2017. http://dx.doi.org/10.1136/sextrans-2017-053264.654.

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Reports on the topic "Health advocacy"

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Howes, Lisa. Climate & environment assessment: Business case for advocacy for primary health care reform (PHC reform), DFID Nigeria. Evidence on Demand, August 2013. http://dx.doi.org/10.12774/eod_hd075.aug2013.howes.

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2

Masulit, Saniata, Marilou Costello, and Sahar Hegazi. Influencing reproductive health policy and programs in the Philippines: Implementing an advocacy model for utilization of operations research. Population Council, 2001. http://dx.doi.org/10.31899/rh4.1199.

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Morris, Julia, Julia Bobiak, Fatima Asad, and Fozia Nur. Report: Accessibility of Health Data in Rural Canada. Spatial Determinants Lab at Carleton University, Department of Health Sciences, February 2021. http://dx.doi.org/10.22215/sdhlab/2020.4.

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To inform the development of an interactive web-based rural health atlas, the Rural Atlas team within the Spatial Determinants Lab at Carleton University, Department of Health Sciences carried out two sets of informal interviews (User Needs Assessment and Tool Development). These interviews were conducted in order to obtain insight from key stakeholders that have been involved in rural health settings, rural health policy or advocacy, or the development of health mapping tools. Interviews took place via video-conferencing software with participants in the spring of 2020.The following report provides a brief summary of the findings of both sets of interviews.
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Talukder, Md, Ubaidur Rob, Laila Rahman, A. K. M. Zafar Khan, Riad Mahmud, Azizul Alim, Ismat Hena, Farhana Akter, and Anup Dey. Incentivizing providers to improve maternal, newborn and child health services in Bangladesh: Pay-for-performance model refinement and advocacy (P4P MRA) final report. Population Council, 2012. http://dx.doi.org/10.31899/rh2.1022.

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5

Shannon, Caitlin S., and Beverly Winikoff. Misoprostol: An emerging technology for women's health—Report of a seminar. Population Council, 2004. http://dx.doi.org/10.31899/rh17.1002.

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On May 7–8, 2001, the Population Council and the Center for Reproductive Health Research & Policy of the University of California, San Francisco, convened a technical seminar in New York City on the use of misoprostol for women’s health indications. The seminar was designed to provide a forum for researchers, providers, women’s health advocates, and educators to exchange information with the goal of advancing the potential of misoprostol to improve women’s health. Participants discussed the state of the art in research, examined current clinical use of misoprostol, and created strategies for the future. The first day focused on scientific and clinical aspects of misoprostol use. The second day’s discussion centered on the future of misoprostol for women’s health, including identifying priorities for research and the role of provider groups and women’s health and advocacy organizations in helping to ensure misoprostol’s continued, appropriate use. At the end of each session, the group had an opportunity to share ideas and discuss unanswered questions. This report covers the key issues raised by each speaker and highlights general areas of discussion among participants.
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S. Abdellatif, Omar, Ali Behbehani, and Mauricio Landin. Luxembourg COVID-19 Governmental Response. UN Compliance Research Group, August 2021. http://dx.doi.org/10.52008/lux0501.

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The UN Compliance Research Group is a global organization which specializes in monitoring the work of the United Nations (UN). Through our professional team of academics, scholars, researchers and students we aim to serve as the world's leading independent source of information on members' compliance to UN resolutions and guidelines. Our scope of activity is broad, including assessing the compliance of member states to UN resolutions and plan of actions, adherence to judgments of the International Court of Justice (ICJ), World Health Organization (WHO) guidelines and commitments made at UN pledging conferences. We’re proud to present the international community and global governments with our native research findings on states’ annual compliance with the commitments of the UN and its affiliated agencies. Our goal as world citizens is to foster a global change towards a sustainable future; one which starts with ensuring that the words of delegates are transformed into action and that UN initiatives don’t remain ink on paper. Hence, we offer policy analysis and provide advice on fostering accountability and transparency in UN governance as well as tracing the connection between the UN policy-makers and Non-governmental organizations (NGOs). Yet, we aim to adopt a neutral path and do not engage in advocacy for issues or actions taken by the UN or member states. Acting as such, for the sake of transparency. The UN Compliance Research Group dedicates all its effort to inform the public and scholars about the issues and agenda of the UN and its affiliated agencies.
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Kenya: Mobilize health care providers to advocate against FGM/C. Population Council, 2007. http://dx.doi.org/10.31899/rh14.1071.

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8

Using evidence to advocate for the professional growth of community health workers in Bangladesh. Population Council, 2021. http://dx.doi.org/10.31899/rh14.1087.

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