Research Advocacy Research Articles

Does justice affect brand advocacy? Online brand advocacy behaviors as a response to hotel customers’ justice perceptions

This study focuses on customers' information-sharing behavior in the context of online brand advocacy behavior regarding hotel brands. We aim to explain hotel customers' online brand advocacy behavior through three-sided justice evaluations (i.e., justice for employees, justice for the self, and global belief in a just world), and their hotel satisfaction. Hypotheses are tested by using survey data acquired from 688 individuals on Amazon's Mechanical Turk (MTurk) through partial least squares structural equation modeling (PLS-SEM). The findings show that customers' perceptions of justice for the self positively affect their hotel satisfaction, perceptions of justice for employees and the global belief in a just world positively affect online brand advocacy behavior, and hotel satisfaction also positively affects online brand advocacy behavior. We expand current research efforts on online brand advocacy research and provide theoretical and managerial implications for the development of marketing and management research and practice.

The Scientific Editor: An Advocate for Transparent Research

If you were to ask a room of editors how they landed a career in scholarly publishing, you might hear a common theme: “I fell into it.” Whether by serendipity or design, a career in this field offers opportunities to do meaningful work, acquire new knowledge, and nurture a fondness of the written word. But at the same time, it’s a vast and constantly evolving ecosystem. What new or emerging opportunities exist? Scientific editing, for one! Specifics will vary depending on the journal, but in general the Scientific (also called Science or Technical) Editor’s role is to work with the handling editors to facilitate the publication of high-quality, highly citable manuscripts that are clear, consistent, and transparent. In this article, Jenna Jakubisin and Kristin Inman discuss scientific editing at their respective publications, highlighting its tremendous value to both authors and journals. Instituting a Science Editor Position: How Does Scientific Editing Benefit Journals? Radiology1 is the flagship journal of the Radiological Society of North America (RSNA), published regularly in-house since 1923. In a typical year, we receive about 3000 submissions. The scientific editor position was created in 2017, an effort spearheaded by the journal’s editor and approved by RSNA’s board of directors. The initial goals were simple but ambitious: Goal 1: Support the journal’s deputy editors. Technical edits had previously been performed by deputy editors (our busy subject matter experts). The use of a Scientific Editor allows them to focus on scientific content rather than language editing. Goal 2: Help improve […]

The Interplay of Challenge-Hindrance-Appraisal and Self-Efficacy: Technostress and Remote Working Performance

Measures to contain the COVID-19 pandemic have caused many employees to work from home; a novel situation in which individuals used information systems (IS) more intensively to stay in touch with coworkers. This novel IS use situation affected individuals differently and resulted in both positive and negative outcomes. Recent calls for research advocate for clarification regarding the conceptualisation of appraisal, which explains different individual responses to objectively equal environments. In particular, challenge-hindrance-research does not differentiate between primary and secondary appraisal. Therefore, it remains unclear how individual capability beliefs, such as self-efficacy, affect challenge and hindrance IS use appraisal. We conduct an empirical study with 1,553 German employees to investigate these relationships and the positive and negative outcomes during the COVID-19 pandemic. We find that challenge and hindrance IS use appraisal, and remote working self-efficacy are interconnected, yet different constructs. We find that self-efficacy is related to challenge IS use appraisal, rather than hindrance IS use appraisal. Further, challenge IS use appraisal is a driver for performance in a remote working environment. We conclude that there are stressful aspects of IS use that are not influenced by an individual’s belief in their abilities. Our study emphasises the importance of remote working self-efficacy and IS use appraisal to mitigate techno-distress and increase performance during remote work.

Employees’ online brand advocacy behaviors as a response to justice and emotion

PurposeThis study aims to focus on the information sharing behavior of employees in the context of online brand advocacy based on the cognition–affection–behavior framework.Design/methodology/approachOnline surveys were distributed to 840 employees, and the gathered data was analyzed by using structural equation modeling.FindingsThe effects of perceived organizational justice, employee emotions, organizational trust on online brand advocacy and the moderating role of organizational identification were empirically supported in this study. Noteworthy exceptions to these findings included the lack of evidence of the effect of informational justice on emotions, the effect of procedural justice on negative emotion and the effect of negative emotion on online brand advocacy.Originality/valueThis study expands brand activism research by investigating online brand advocacy and the employee context. Moreover, this work also extends online brand advocacy research through the employee points of view.

Analysis on Data Governance Policy in the Health Sector of Zambia: Perspective of Big Data

The study explored the data governance policy in Zambia's health sector, focusing on big data. To fully realize the potential of data in our digital age, proper data governance is required. However, questions have been expressed concerning Zambia's health sector's ability to exploit data as a valuable resource due to the state of data governance. This study attempts to address this critical issue and shed light on the functions of big data governance aspects in the health sector. This work is significant because it has the potential to improve healthcare service quality, decision-making, and resource allocation through strong data governance. This study aims to bridge the gap between data governance and the requirements of big data in the Zambian health sector by reviewing existing policies, procedures, and practices. A mixed methods approach is used in the research, involving qualitative interviews with key informants and secondary data analysis. To get a full understanding of data governance difficulties, practices, and their alignment with big data demands, thematic and content analysis methodologies were used. The findings show that data governance is critical to managing data in the health sector, yet gaps in governance procedures impede the efficient implementation of ICT efforts. These concerns are exacerbated by challenges relating to competent human resources and ICT infrastructure. Accountability and transparency are also identified as areas for improvement. While this study offers insight on the existing state of affairs, it recognizes its limits and advocates for further research to investigate specific aspects of policy implementation. Nonetheless, this study contributes significantly to the field of big data and data governance in the Zambian health sector, encouraging stakeholders to work for an ICT driven, data-governed future that promotes openness, accountability, and improved healthcare results. Finally, this article emphasizes the importance of improving data governance procedures in Zambia's health sector, as well as the transformative potential of big data in healthcare as a catalyst for good change in the country's healthcare environment.

Abstract IA002: How patient advocates can make a difference in their research advocacy efforts and contributions and why it's important

Abstract Knowledge about cancer research has driven me to advocate on behalf of myself and others who need to know about their cancer risk, hereditary pre-disposition, prevention and survivorship. Understanding how Patient Advocates can make a difference is extremely important and valuable to research. Citation Format: Wenora Y. Johnson. How patient advocates can make a difference in their research advocacy efforts and contributions and why it's important [abstract]. In: Proceedings of the 15th AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; 2022 Sep 16-19; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2022;31(1 Suppl):Abstract nr IA002.

Effects of motor pacing on frontal-hemodynamic responses during continuous upper-limb and whole-body movements.

Advances in timing research advocate for the existence of two timing mechanisms (automatic vs. controlled) that are related to the level of cognitive control intervening for motor behavior regulation. In the present study, we used the functional near-infrared spectroscopy (fNIRS) cutting-edge technique to examine the hypothesis that prefrontal inhibitory control is needed to perform slow motor activities. Participants were asked to perform a sensorimotor-synchronization task at various paces (i.e., slow, close-to-spontaneous, fast). We contrasted upper-limb circle drawing to a more naturalistic behavior that required whole-body movements (i.e., steady-state walking). Results indicated that whole-body movements led to greater brain oxygenation over the motor regions when compared with upper-limb activities. The effect of motor pace was found in the walking task only, with more bilateral orbitofrontal and left dorsolateral activation at slow versus fast pace. Exploratory analyses revealed a positive correlation between the activation of the orbitofrontal and motor areas for the close-to-spontaneous pace in both tasks. Overall, results support the key role of prefrontal cognitive control in the production of slow whole-body movements. In addition, our findings confirm that upper-limb (laboratory-based) tasks might not be representative of those engaged during everyday-life motor behaviors. The fNIRS technique may be a valuable tool to decipher the neurocognitive mechanisms underlying naturalistic, adaptive motor behaviors.

Exploring institutional logics to dynamic ambidexterity in health information system implementation in the public health sector of Ethiopia

AbstractInformation system (IS) implementation can often lead to inherently contradictory issues, standardization, and evolve‐ability, which requires different, sets of information technology (IT) governance mechanisms. Recent research advocate ambidexterity mechanisms which consider the contradictory logic for long‐term success yet it has paid little attention to resource‐constrained settings which is a source of contradiction for the lack of technical and financial resource. Using an interpretative approach, based on institutional logic and dynamic ambidexterity concepts, this study revealed how centralized, systemic, and IT logics shaped IT governance mechanisms toward centralized and ad hoc‐based decentralized structures. Furthermore, the study depicted how the lack of a common vision for IS implementation impeded defining roles, identifying and collaborating with similar initiatives that led the implementation to uncontrolled evolve‐ability. Despite the absence of a common vision in resource‐constrained settings, the study identified the importance of resource‐chasing collaboration among heterogeneous actors to achieve standardization and evolve‐ability at a certain level though not sufficient. The study proposed an ambidextrous implementation framework by combining dynamic ambidexterity and institutional logic concepts to complement the resource‐chased collaboration with major HIS logics‐based collaboration through devising common vision, strategy, and mechanisms which allows sensing, seizing, and reconfiguring the emergent heterogeneous system implementation initiatives to achieve standardization and evolve‐ability simultaneously.

Exploring Nonprofit Advocacy Research Methods and Design: A Systematic Review of the Literature

The study of nonprofit advocacy has evolved significantly over the past two decades, yet gaps still remain in our understanding of the processes and roles of nonprofit organizations in policymaking and policy change. In part, these gaps may be exacerbated by limitations in the methodologies and research designs used to examine advocacy, despite the growing scholarship base. To investigate this possibility, this article reports the findings of a systematic literature review of 264 scholarly articles that examine the antecedents, processes, and/or outcomes of nonprofit advocacy. The sampling method relies heavily on scholarship published in six leading nonprofit and public administration journals. Although theory suggests that nonprofit organizations have a vital role in facilitating policy processes, much of the advocacy research relies upon a limited form of research questions and methods. Findings also reveal a need for greater precision in describing data, design, and methods, and suggest a need for clearer, validated measures of both nonprofit advocacy efforts and the resulting outcomes. Finally, we suggest new areas for nonprofit advocacy research, including investigating new venues, different levels of analysis, employing emerging research methods, and examining advocacy over time.

LibParlor Online Learning

Learning how to conduct research in library and information science is not always a requirement in LIS graduate programs. The result of uneven training impacts librarianship and the ways in which certain voices and research are privileged in our scholarship. This work in progress poster will share the results of an IMLS grant funded national needs assessment wherein we learned about the experiences, educational needs, and institutional constraints of MLIS students and academic library workers pursuing research through a survey and focus groups. The poster will share insights on the experiences of academic library workers and their needs for institutional, educational, and financial support for training and advocacy in LIS research. We will share information about what LIS researchers feel they benefited from their graduate coursework in research methods, as well as ideas for improvement for these courses.

Advocating for Research and Using Research for Advocacy

Advocating for Research and Using Research for Advocacy

Palliative Care Early in the Care Continuum among Patients with Serious Respiratory Illness: An Official ATS/AAHPM/HPNA/SWHPN Policy Statement.

Background: Patients with serious respiratory illness and their caregivers suffer considerable burdens, and palliative care is a fundamental right for anyone who needs it. However, the overwhelming majority of patients do not receive timely palliative care before the end of life, despite robust evidence for improved outcomes. Goals: This policy statement by the American Thoracic Society (ATS) and partnering societies advocates for improved integration of high-quality palliative care early in the care continuum for patients with serious respiratory illness and their caregivers and provides clinicians and policymakers with a framework to accomplish this. Methods: An international and interprofessional expert committee, including patients and caregivers, achieved consensus across a diverse working group representing pulmonary-critical care, palliative care, bioethics, health law and policy, geriatrics, nursing, physiotherapy, social work, pharmacy, patient advocacy, psychology, and sociology. Results: The committee developed fundamental values, principles, and policy recommendations for integrating palliative care in serious respiratory illness care across seven domains: 1) delivery models, 2) comprehensive symptom assessment and management, 3) advance care planning and goals of care discussions, 4) caregiver support, 5) health disparities, 6) mass casualty events and emergency preparedness, and 7) research priorities. The recommendations encourage timely integration of palliative care, promote innovative primary and secondary or specialist palliative care delivery models, and advocate for research and policy initiatives to improve the availability and quality of palliative care for patients and their caregivers. Conclusions: This multisociety policy statement establishes a framework for early palliative care in serious respiratory illness and provides guidance for pulmonary-critical care clinicians and policymakers for its proactive integration.

Women cancers in India: Incidence, trends and their clinical extent from the National Cancer Registry Programme

BackgroundTo provide a comprehensive assessment of women cancer in India utilizing the systematically collected data on all cancers by the National Cancer Registry Programme (NCRP). MethodsThe study examined 10,2287 cancer cases among women cancers providing cancer burden for major anatomical sites. Aggregated data of 28 PBCRs and 58 HBCRs under NCRP for 2012–16 was analysed for incidence rates, trends, cumulative risk of developing cancer, stage at detection and treatments offered. ResultsStudy results have found region –wide variation of women cancers by indicating highest proportions in western followed by southern region of India. North-Eastern region had lowest proportion. It was observed that breast is highest ranking cancer in most registry areas of urban agglomerations of country while cancer cervix was leading site in registries of rural areas like Barshi (15.3) and Osmanabad &Beed (13.1). States of Mizoram (23.2) and Tripura (9.5) along with Pasighat, Cachar and Nagaland. Median age of occurrence for women for these anatomical sites ranged from 45 to 60 years of age. For cancer breast, cervix and ovary –most cases were detected with regional spread. These findings were different for cancer corpus uteri where registries have reported higher proportions (49.3 %) of localized stage at detection. Loco regional cancers had higher proportions of multimodality treatments. ConclusionStudy provides a foundation for assessing the status of women cancers in the country. Variations between geographies would guide appropriate support for action to strengthen efforts to improve cancer prevention and control in underserved areas of the country. This would facilitate advocacy for better investments and research on women cancers.

Supporting the Primary Care Research Infrastructure Through Advocacy: A Reflection from the NAPCRG Research Advocacy Committee.

Whether it’s running among the saguaro cacti in Tucson, hiking up Mont Royal in Montreal, or listening to Bill Hogg play the drums, it’s the moments with friends that we remember the most fondly. These are the serendipitous encounters where connections are strengthened and research plans are

Are media covering while women are campaigning? A study of Mexican municipal elections

ABSTRACT Studies on media coverage have found that female nominees receive unequal treatment regarding their visibility and portrayal of their agendas. To assess how media cover women, municipal elections in Mexico are analysed. By focusing on municipal elections, this research advocate for the study of local phenomena and their discourses. The study questions whether women have received equal media exposure compared to men. The research analyses how women are portrayed and explores how print news media present stories about women and the narratives included in their stories. Findings suggest that female and male candidates are equally visible, but men are singled out more often as likely winners. News reports focus mostly on ‘male’ issues, but coverage does not focus disproportionally on female candidates’ personality traits.

Analyzing Police Communication Strategies for Preventing Teenage Drug Abuse in Simpang Kanan Subdistrict, Rokan Hilir Regency

This research delves into the efficacy of police communication strategies in combating drug abuse among teenagers in Simpang Kanan Subdistrict, situated within the Rokan Hilir Regency of Indonesia. Utilizing a mixed-methods approach, the study navigates the intricate interplay of cultural dynamics, community engagement, and the effectiveness of varied communication channels employed by law enforcement agencies. Quantitative analysis unveils statistical trends in drug abuse prevalence among teenagers, shedding light on the impact of specific communication strategies. Concurrently, qualitative exploration delves into perceptions, experiences, and stakeholder feedback, offering depth to the understanding of the multifaceted issue. Findings underscore the strengths of community engagement initiatives and diverse communication channels, showcasing heightened awareness and positive behavioral shifts among teenagers. Yet, limitations such as data constraints, sampling intricacies, and resource limitations temper the comprehensiveness of the analysis. The implications drawn from this research advocate for tailored, culturally sensitive approaches, community-driven interventions, and continuous evaluation mechanisms in future policy changes. These insights transcend regional boundaries, offering a framework adaptable to analogous contexts worldwide. This research serves as a beacon, illuminating pathways toward combating teenage drug abuse.

Epilepsy research in Africa: A scoping review by the ILAE Pediatric Commission Research Advocacy Task Force.

Despite the high prevalence of epilepsy in Africa, evaluation of epilepsy research trends on the continent is lacking. Without establishing effective research, improvement in care for people with epilepsy cannot be effectively strategized or targeted. A scoping review of the peer-reviewed literature on epilepsy from Africa (1989-2019) was conducted. The aim was to understand from this what areas are well researched versus underresearched based on published epilepsy topics. A total of 1227 publications were identified and assessed. A significant increase in publications occurred over the 30 years assessed. African author leadership was evident in most reports. Nine countries had >50 publications identified; the remaining 45 countries had <50 or no publications. Research studies were typically of lower quality (case series and observational studies). Research themes were more focused on clinical epilepsy (descriptive observational studies) and social aspects (qualitative surveys). However, there were a number of unique and strong themes, specifically for neurocysticercosis and nodding syndrome, where strong research collaborations were evident, basic science understandings were explored, and interventional models were established. Despite Africa being the continent with the most countries, it is lacking in the quantity, quality, and for some areas, relevance of research on epilepsy. Targeted approaches are needed to upskill the strength of research undertaken with more basic science, interventional, and randomized controlled studies. Themes of research need to promote those with unique African content but also to align with current international research areas that have impact on care delivery, such as epilepsy surgery and epilepsy genetics. For this to be possible, it is important to strengthen research hubs with collaborations that empower Africa to own its epilepsy research journey.

Abstract 1014: A framework for research scientists to include patient advocates in cancer research

Abstract The inclusion of patient advocates in basic cancer research has emerged as a valuable practice to ensure research is intentional, to support effective communication with broader audiences, and to directly connect researchers with those whom they are striving to help. Despite this value, many researchers do not work with patient advocates. To understand why and build a roadmap for more engagement in the future, we hosted a workshop with patient advocates and research scientists then presented findings and discussed further at an international conference. We acknowledged four main barriers: 1) It is not clear to everyone why patient advocates should be included in research, 2) Researchers are worried about saying the wrong thing, 3) Researchers do not know where to meet patient advocates, and 4) Researchers do not know how to include patient advocates in research. We identified best practices from various organizations and opportunities to overcome these barriers in the short- and long-term. This is the first time a multi-stakeholder group has come together to provide ways to support research scientists with overcoming barriers to regularly working with patient advocates. Ultimately, these relationships will improve cancer research and more quickly accomplish our collective goal of improving lives of those who have been diagnosed with cancer. Citation Format: Hillary Stires, Igor Bado, Thelma Brown, Martha Carlson, Isaac S. Chan, Gloria V. Echeverria, Andrew J. Ewald, Carla Lloyd, Julia Maues, Steffi Oesterreich, Robert N. Riter, Kelly Shanahan, Alana L. Welm, Josh Newby. A framework for research scientists to include patient advocates in cancer research [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 1014.

JOB ANALYSIS FOR PERSONS WITH DISABILITIES IN STATE CIVIL APPARATUS NEEDS PLANNING

As a form of respect and fulfillment of the rights of persons with disabilities in working, the Government issued an affirmation policy by opening the formation of persons with disabilities as the Aparatur Sipil Negara-ASN (State Civil Apparatus). In the implementation of ASN recruitment, there are several problems faced, including the formation of persons with disabilities that are not filled and requirements that have not accommodated the interests of persons with disabilities. One problem is the non-fulfillment of the formation, or the tan caused by the job analysis. This study aims to describe the process of job analysis for persons with disabilities in the recruitment and selection of ASN with a type of narrative descriptive research. Data collection was carried out through interviews with informants from the Ministry of State Apparatus Empowerment and Bureaucratic Reform, the State Civil Service Agency, the Ministry of Social Affairs and Australia Indonesia Disability Research Advocacy Network and document studies by reviewing the literature on job analysis for persons with disabilities and regulations related to job analysis. The results showed that the process of analyzing job analysis of jobs in the context of planning ASN needs as stipulated in the Peraturan Menteri Pemberdayaan Aparatur Negara dan Reformasi Birokrasi Nomor 1 Tahun 2020 concerning Job analysis and Workload Analysis does not specifically regulate for persons with disabilities. The availability of facilities and the lack of a comprehensive understanding of the issue of inclusivity in the fulfillment of the right to work for persons with disabilities are factors in the emergence of job requirements that are not accommodating to all kinds of disabilities. The provision of accessibility and decent accommodation has not been a major concern in the preparation of the ASN job analysis.

100 plus years of stem cell research-20 years of ISSCR.

SummaryThe International Society for Stem Cell Research (ISSCR) celebrates its 20th anniversary in 2022. This review looks back at some of the key developments in stem cell research as well as the evolution of the ISSCR as part of that field. Important discoveries from stem cell research are described, and how the improved understanding of basic stem cell biology translates into new clinical therapies and insights into disease mechanisms is discussed. Finally, the birth and growth of ISSCR into a leading stem cell society and a respected voice for ethics, advocacy, education and policy in stem cell research are described.