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Whatever their private religious convictions, nearly all contemporary psychologists of religion – when they act in professional roles – agree to operate in accordance with scientific rules. Recognition of the imperfections of individual methodologies has led to an emphasis on testing theories and verifying “facts” in multiple studies. Most of this chapter explores the pros and cons associated with various research methods, including experimentation, observation, and survey research. Although the logic of experimentation is undeniable and psychologists in various subfields frequently deem it the method of choice, many questions that we most want to answer in the psychology of religion cannot be addressed through experiments that are feasible, ethical, and convincing. Thus, the psychology of religion has always relied heavily on quantitative and qualitative survey research studies. Good surveys must strive to avoid biases rooted in question wording, question order, mode of data collection, social desirability, attitude-behavior discrepancies, and the tendency to overreport religious behavior. Fortunately, many existing measures of religious attitudes and behaviors have good psychometric qualities.
Baby boomers were at the forefront of profound social changes in sexual attitudes and many have expressed a desire to remain sexually active throughout their life course. The purpose of this survey study was to assess the perceived preparedness of Ontario’s long-term care (LTC) homes to meet the changing sexuality needs and expectations of LTC residents. We examined sexuality-related attitudes, including in the context of dementia, among 150 LTC administrators. Participants also completed a questionnaire assessing their experiences and perceptions regarding existing and anticipated supports, barriers, and priorities. Most participants demonstrated positive sexual attitudes; however, multiple challenges to meeting residents’ sexuality needs were noted, including assessing capacity to consent, limited privacy, staff training, conflicting attitudes, and a lack of adequate policy and guidelines. Challenges are broad and significant and considerable attention is required to meet the expectations of the next generation of LTC residents, including gender and sexual minority elders.
This chapter is structured in four parts. First, the chapter reviews current approaches to the integration challenge and makes the case for a pragmatist approach. Second, it uses pragmatism to differentiate qualitative and quantitative research purposes and show how these purposes can be integrated to produce a more granular conceptualization of the synergies within simultaneous, sequential, and recursive designs. Third, it considers the question of creativity in mixed methods designs as a consequence of adopting a pragmatist standpoint. The chapter ends with a set of implications for mixed methods research and a call for new and creative methodologies in this area.
The main quantitative research designs are reviewed, to indicate their strengths and limitations. Even the best designed and conducted studies run the risk of being influenced by the ever-present threats of chance, bias, and confounding, terms that are explained and illustrated with examples, and of sampling and measurement error. The informed reader should therefore look beyond the results of a study, using critical appraisal skills to ask whether the study’s design, sample, and measures are robust enough to allow the findings to be taken as likely to be accurate.
This chapter understands the Linguistic Landscape (LL) as a flow of discourse in time. LL units are structured as texts, materials, and discourse, but the LL only unfolds when these units engage the sign instigator and the sign viewer in discourse in the public eye. Using the foodscape as a focal point, the boundaries between the LL and other social practices are examined. A review of LL research methodology examines the role of photographs and the photographer’s point of view, fieldwork approaches that include interviews and reflexive ethnography, and the position of quantitative analysis. The chapter discusses relationships between the material LL and online linguistic landscapes (OLL), examining language displays in the OLL and ways in which users transcend the apparent boundaries between the two. Pointing out the long history of representing the LL in literature, the chapter discusses James Joyce’s Ulysses for its portrayal of the outer forms of the LL and its representation of the inner world of characters who move through the LL. Recommendations are made for further expansion of the field geographically, temporally, materially, and ethnographically.
The chapter ’Going on Pawtrol’ describes how to conduct linguistic research using the cat examples from the original research done for this book. It looks at methodological issues, like research design, research methods, sampling methods, data collection, wordlists, and surveys. The chapter also discusses ethics in relation to the protection of research participants and the research, touching on the laws in place to protect people’s privacy and data and the ethical guidelines established for researchers.
The chapter discusses how quantitative and qualitative methods can be combined, outlines their strengths and limitations, and introduces four qualitative approaches of linguistic analysis: version analysis, progression analysis, variation analysis, and metadiscourse analysis. Together, the four approaches enable researchers to understand language use in digital media environments from multiple angles. Furthermore, the chapter provides an insight into visual content analysis, semiotics, and iconography/iconology. For multimodal analysis, a three-stage method is presented. Finally, the chapter discusses how the multimodal text relates to a certain text genre and to the social context of which it is a part.
There is mixed evidence regarding the direction of a potential association between post-traumatic stress disorder (PTSD) and suicide mortality.
Aims
This is the first population-based study to account for both PTSD diagnosis and PTSD symptom severity simultaneously in the examination of suicide mortality.
Method
Retrospective study that included all US Department of Veterans Affairs (VA) patients with a PTSD diagnosis and at least one symptom severity assessment using the PTSD Checklist (PCL) between 1 October 1999 and 31 December 2018 (n = 754 197). We performed multivariable proportional hazards regression models using exposure groups defined by level of PTSD symptom severity to estimate suicide mortality rates. For patients with multiple PCL scores, we performed additional models using exposure groups defined by level of change in PTSD symptom severity. We assessed suicide mortality using the VA/Department of Defense Mortality Data Repository.
Results
Any level of PTSD symptoms above the minimum threshold for symptomatic remission (i.e. PCL score >18) was associated with double the suicide mortality rate at 1 month after assessment. This relationship decreased over time but patients with moderate to high symptoms continued to have elevated suicide rates. Worsening PTSD symptoms were associated with a 25% higher long-term suicide mortality rate. Among patients with improved PTSD symptoms, those with symptomatic remission had a substantial and sustained reduction in the suicide rate compared with those without symptomatic remission (HR = 0.56; 95% CI 0.37–0.88).
Conclusions
Ameliorating PTSD can reduce risk of suicide mortality, but patients must achieve symptomatic remission to attain this benefit.
Due to the shift to the social model of health care, public health researchers and practitioners are increasingly interested in the insider perspectives and experiences of key players in health, including health consumers and healthcare providers (Olson, Young & Schultz, 2016). Thus, qualitative research has been adopted in public health in many ways and in numerous fields of health research. The main focus of this chapter is on qualitative research. You will learn about the nature of qualitative inquiry and the need for qualitative research in public health. You will also gain a basic understanding of some philosophical assumptions of qualitative research that lead to different understandings about public health in different groups of people. Attempts have been made in the past few decades to provide evidence-based public health care to individuals and communities. Thus, we have witnessed a large number of research projects carried out in the public health arena. Evidence-based practice in public health and the need for qualitative inquiry are also discussed in this chapter.
Political science (PSCI) is housed in the social sciences, which together “examine what it means to be a social being, ranging from the minutiae of human behavior … to large scale social movements, demographics, economics and politics” (European Science Foundation, 2016). Undergraduate research (UR) in PSCI, whether using quantitative, qualitative or mixed methods, helps students develop critical thinking skills and tools, whereby they can apply what they learn in class to the real world, rather than just memorizing facts and figures that are forgotten after they take each semester exam.
The chapter describes the assumptions and goals of large n statistical studies and evaluates the extent to which they generate knowledge about international relations.
This review covers the thematic series of 22 papers selected from among manuscripts published by BJPsych Open concerning coronavirus disease 2019 (COVID-19) and healthcare. We report nine papers that cover concepts and epidemiology relating to the public and patients. We review 11 papers about the impact of COVID-19 on healthcare services and their staff in 15 countries. Two papers consider the psychosocial impact on staff working in mental health services in the UK. Most papers report cross-sectional analyses of data collected from convenience samples by self-reported surveys conducted at single times. They have limitations of generalisability, do not enable conclusions about diagnosis or causality, and many are likely to have attendant bias and noise. BJPsych Open published these papers to meet requirements for early indications of the mental health impact of COVID-19 on the public and on healthcare staff. They claim high prevalence of symptoms of anxiety, depression and post-traumatic stress. We contrast these findings with selected reports of studies with different methodologies published elsewhere. We emphasise the need for longitudinal clinical studies with refined sampling and methodological rigour. We identify several longitudinal research programmes; two in this series. We advocate tuning advice offered about caring for the public and healthcare staff to the realities of their circumstances and their perceptions of need in the context of findings from further longitudinal studies. We draw attention to the importance of the social, relationship and environmental circumstances of the public and healthcare staff in order to understand their distress and their risks of developing mental health disorders.
Chapter 4 provides a summary of the datatypes studied in cross-cultural pragmatics and the fundamental methodologies used in the field. First, we systematically discuss different types of data, by arguing that the conventional categories of ‘naturally occurring’ and ‘elicited’ data are equally important for cross-cultural pragmatic research. The relationship between these two categories is particularly important to discuss: while using elicited data has been subject to major criticisms in the field of pragmatics, we promote an inclusive cross-cultural pragmatics approach, which should not exclude any datatype. Following our overview of datatypes, we summarise qualitative and quantitative approaches frequented in the field. The chapter explains in detail why it is pivotal for the cross-cultural pragmatician to attempt to combine qualitative and quantitative research if she wants to compare language use in a rigorous and replicable way.
This chapter focuses on quantitative research that is Indigenous-led and Indigenous-focused. It begins by discussing quantitative research in the context of Indigenous people to reject the commonly held assumption that quantitative research methods are less appropriate than quantitative methods in Indigenous contexts. It considers the importance of using an Indigenous methodology rather than a Western research methodology. The chapter differentiates between various research methodologies before focusing on the Indigenous research methodology in Australia. It highlights the importance of working with Aboriginal and Torres Strait Islander communities, considering Indigenous worldviews during research, and conducting research with political integrity. The chapter uses two case studies of Indigenous quantitative research to guide readers through the process and explain how to display and interpret results, and provides detailed guidance on using chi-squared tests to interpret results.
The Coronavirus disease (COVID-19) health emergency has led national states to adopt severe actions forcing many people to cope with new and unexpected challenges. Those constraints risked to jeopardized the mental health and subjective wellbeing (SWB) of individuals.
Objectives
The present cross-sectional quantitative study explored whether and to what extent psychological and social aspects were determinants of parental SWB as outcome variable during the COVID-19 lockdown.
Methods
The sample was composed of 304 Italian parents (93% female, mean age 41.5, 91% from Lombardy). Data were gathered through Computer Assisted Web Interview (CAWI) four weeks after the beginning of the national lockdown. World Health Organization (WHO) wellbeing scale along with other self-reported measures of social support, feelings of abandonment, feeling of being equipped and adequacy of living spaces were administered. Data were analyzed by hierarchical regression models (Ethics Committee of Milano-Bicocca University approval N.0034537/20)
Results
According to the WHO cutoff score, 37.7% of parents reported low well-being levels. The regression model (F=11.2, p<.001) suggested that the feeling of abandonment and the feeling of being equipped were the most important contributors to SWB. Other statistically significant (but with lower effect sizes) variables were the support received by the partner and the adequacy of living spaces.
Conclusions
The findings bear out the pivotal importance of subjective states (such as feelings of abandonment or perceptions of being poorly equipped) in relation to the levels of parental SWB during the COVID-19 lockdown. Implications for planning psychological interventions aimed at strengthening personal resources to face the emergency are discussed.
The demographic landscape of European countries is rapidly changing because of population ageing; in this context, societies are called to offer older people opportunities to age actively. Although ‘active ageing’ has been broadly explored, there is still room to further our knowledge on the individual conditions that may favour or hinder activity in later life. This study aims to contribute to the literature in this field by focusing on the role of social capital. Specifically, it explores, through logistic regression models, how social capital and changes in social capital are associated with engagement in, the initiation of and continued participation in various domains of activity: volunteering and charity work, active participation in political or community-related organisations, informal care-giving and paid work. The data analysed stem from the Survey of Health, Ageing and Retirement in Europe (SHARE). We focused on people aged 55+ participating in Waves 4–6. The key findings are: (a) having a larger social network is positively associated with participation in and the initiation of activities; (b) receiving social support (rarely) may stimulate reciprocity and thus care-giving; and (c) an increase in social network size is positively associated with initiation and maintenance of activities during later life.
Since the Anglican Church in England and Wales began to build schools long before the state developed machinery to do so, around a quarter of all primary schools remain connected with the Anglican Church. The church school inspection system maintains that Anglican schools have a distinctive ethos. The Student Voice Project argues that school ethos is generated by the implicit collective values, beliefs and behaviours of the students, and was designed to give explicit voice to the students in response to six specific areas of school life identified by the Anglican school inspection criteria as relevant to school ethos. Drawing on data provide by 8,111 year-five and year-six students attending Church in Wales primary schools, the present study reports on the six ethos measures and on significant differences reported by female and male students, and by year-five and year-six students.
China has faced challenges related to the rapid growth of its ageing population, and sleep is one of the public health challenges to this demographic group. This study examines the socio-demographic and behavioural factors associated with status change of sleeping patterns among Chinese older adults, using longitudinal data from the Chinese Longitudinal Healthy Longevity Survey (CLHLS). Socio-demographic factors were selected from the 2012 wave of the CLHLS to examine the sleep status change in the 2014 wave. Multivariable logistic and multinomial regressions were used to study older adults’ changes of sleep quality and daily sleep duration. Older adults, 65 years old or above, were selected as study participants. A higher level of education was negatively associated with poor sleep quality and longer sleep duration (>8 hours). Increasing age was positively associated with both shorter and longer sleep duration. Being female was negatively associated with longer sleep duration. However, exercise status, smoking behaviour and alcohol use all were neither positively nor negatively associated with status change of sleeping patterns. Participants’ education, age and gender might be important factors associated with sleep status change. However, the effects of behavioural factors should be studied further. Policy implications and further research directions are discussed based on empirical results.
Excessive worry can negatively influence one’s developmental trajectories. In the past 70 years, there have been studies aimed towards documenting and analysing concerns or ‘worries’ of teen and preteen individuals. There have been many quantitative and qualitative approaches established, suggesting different themes of contextual adolescent worry. With the hopes of future clinical utility, it is important to parse through these studies and gather what is currently known about what teens and preteens worry about and what is the state of methods used to gather that knowledge. Studies were searched for using Web of Science, PubMed, PsycINFO, Scopus and ScienceDirect databases and selected on systematic criteria. Data regarding the country in which the study took place, participants, methods of collection, worry themes and conclusions and limitations were extracted. Data were synthesised in a narrative fashion. It was concluded that currently available methods of measuring themes of adolescent worry face certain problems. Themes of worry differ substantially between the studies, with the exception of school performance seeing stable high endorsement across cultures and ages. Issues with ordering worry themes and implications for future understanding of adolescent and preadolescent worry are discussed.
For the past 4 years, as part of the National Institutes of Health (NIH) Clinical and Translational Science Award (CTSA) grant award number UL1TR001436, the Clinical Translational Science Institute of Southeast Wisconsin (CTSI) has used process engineering approaches to identify and understand barriers that local researchers and other stakeholders face when engaging in clinical and translational science. We describe these approaches and present preliminary results. We identified barriers from published and unpublished work at other CTSA hubs, supplemented by surveys and semi-structured interviews of CTSI faculty. We then used a multifaceted approach to organize, visualize, and analyze the barriers. We have identified 27 barriers to date. We ranked their priority for CTSI to address based on the barrier’s impact, the feasibility of intervention, and whether addressing the barrier aligned with CTSI’s institutional role. This approach provides a systematic framework to scope and address the “barriers to research problem” at CTSI institutions.