scholarly journals A Life Space Perspective to Approach Individual Demographic Processes

2010 ◽  
Vol 37 (1-2) ◽  
pp. 207 ◽  
Author(s):  
Éva Lelièvre ◽  
Nicolas Robette

The concept of life space refers to the different locations with which individuals interact along their life course. In this article we present several methodological proposals to describe and measure various territories to which individuals relate over time, taking advantage of a rich data source, the Biographies et entourage survey. We produce relevant indicators which can be used in the study of different demographic processes and demonstrate how this perspective elegantly formalizes the linked dynamics of interactive non-independent trajectories in the case of the couples’ activity space.

PLoS ONE ◽  
2018 ◽  
Vol 13 (8) ◽  
pp. e0201223 ◽  
Author(s):  
Michelle Degli Esposti ◽  
Jonathan Taylor ◽  
David K. Humphreys ◽  
Lucy Bowes

Author(s):  
Michelle Degli Esposti ◽  
David K Humphreys ◽  
Lucy Bowes

Background Child maltreatment is a major public health problem affecting one quarter of children in England and Wales. Good epidemiological data are needed to establish how many and which children are most at risk, and to evaluate the impact of policies and interventions. However, a comprehensive data source on child maltreatment is currently lacking. Aim We aimed to create a rich data source on the incidence of Child maltreatment over Time (iCoverT) in England and Wales. Methods We developed systematic methods to search and identify administrative data sources that regularly measured child maltreatment. Data sources were investigated and assessed against pre-specified eligibility criteria and a bespoke quality assessment tool. Relevant data were extracted, digitalised, and harmonised over time. All data and their accompanying documentation were prepared to form an open access data source: the iCoverT (osf.io/cf7mv). Results We identified 13 unique sources of administrative data, six of which met our eligibility criteria: Child protection statistics, Children in care, Criminal statistics, Homicide index, Mortality statistics and NSPCC statistics. Data and documentation were prepared and combined to form the iCoverT, including 272 variables, over 43,500 data points, and spanning over 150 years. A subsequent time series analysis demonstrated the utility of the iCoverT; identifying large overall decreases in child maltreatment from 1858 to 2016 (e.g. 90% decrease in child homicides (2.7 per fewer per 100,000 children)) but worrying recent increases from 2000 to 2016. Conclusion We systematically developed a rich data source on child maltreatment in England and Wales. Our methodology overcomes practical obstacles and offers a new approach for harnessing administrative data for research. Our resulting data source is a valuable public health surveillance tool, which can be used to monitor national levels of child maltreatment and to evaluate the effectiveness of child protection initiatives.


Author(s):  
Laurie Cohen ◽  
Joanne Duberley

Laurie Cohen and Joanne Duberley describe their use of an unconventional data source—a radio programme—to study celebrity careers. This source also includes music, which evokes memories, and elicits emotions not readily captured in conventional interviews. They used the archives of the BBC Radio 4 programme Desert Island Discs to study the careers of well-known research scientists. The programme’s format has been consistent over its 70-year history; ‘castaways’ from all walks of life are interviewed about their careers and are asked to select eight pieces of music, which reveal many other aspects of their lives. This research focused on the relationships between work and life course, the notion of career as performance, and the role of emotion in the narration of career. Desert Island Discs is part of an extensive archive. As time and funding for research are tight, rapid no-cost access to such data is valuable.


2021 ◽  
pp. 095269512199539
Author(s):  
Penny Tinkler ◽  
Resto Cruz ◽  
Laura Fenton

Birth cohort studies can be used not only to generate population-level quantitative data, but also to recompose persons. The crux is how we understand data and persons. Recomposition entails scavenging for various (including unrecognised) data. It foregrounds the perspective and subjectivity of survey participants, but without forgetting the partiality and incompleteness of the accounts that it may generate. Although interested in the singularity of individuals, it attends to the historical and relational embeddedness of personhood. It examines the multiple and complex temporalities that suffuse people’s lives, hence departing from linear notions of the life course. It implies involvement, as well as reflexivity, on the part of researchers. It embraces the heterogeneity and transformations over time of scientific archives and the interpretive possibilities, as well as incompleteness, of birth cohort studies data. Interested in the unfolding of lives over time, it also shines light on meaningful biographical moments.


2020 ◽  
Vol 11 (05) ◽  
pp. 769-784
Author(s):  
Ipek Ensari ◽  
Adrienne Pichon ◽  
Sharon Lipsky-Gorman ◽  
Suzanne Bakken ◽  
Noémie Elhadad

Abstract Background Self-tracking through mobile health technology can augment the electronic health record (EHR) as an additional data source by providing direct patient input. This can be particularly useful in the context of enigmatic diseases and further promote patient engagement. Objectives This study aimed to investigate the additional information that can be gained through direct patient input on poorly understood diseases, beyond what is already documented in the EHR. Methods This was an observational study including two samples with a clinically confirmed endometriosis diagnosis. We analyzed data from 6,925 women with endometriosis using a research app for tracking endometriosis to assess prevalence of self-reported pain problems, between- and within-person variability in pain over time, endometriosis-affected tasks of daily function, and self-management strategies. We analyzed data from 4,389 patients identified through a large metropolitan hospital EHR to compare pain problems with the self-tracking app and to identify unique data elements that can be contributed via patient self-tracking. Results Pelvic pain was the most prevalent problem in the self-tracking sample (57.3%), followed by gastrointestinal-related (55.9%) and lower back (49.2%) pain. Unique problems that were captured by self-tracking included pain in ovaries (43.7%) and uterus (37.2%). Pain experience was highly variable both across and within participants over time. Within-person variation accounted for 58% of the total variance in pain scores, and was large in magnitude, based on the ratio of within- to between-person variability (0.92) and the intraclass correlation (0.42). Work was the most affected daily function task (49%), and there was significant within- and between-person variability in self-management effectiveness. Prevalence rates in the EHR were significantly lower, with abdominal pain being the most prevalent (36.5%). Conclusion For enigmatic diseases, patient self-tracking as an additional data source complementary to EHR can enable learning from the patient to more accurately and comprehensively evaluate patient health history and status.


2012 ◽  
pp. 193-207
Author(s):  
Steven G. Medema

Historians of economics have paid minimal attention to the diffusion of economic ideas in the textbook literature. Given the low esteem in which textbooks are held as embodiments of scholarship and the propensity of historians of economics - and intellectual historians generally - to focus on the production of scholarship through more lofty venues such as journal articles and scholarly books, this lack of attention to the textbook literature is in some ways understandable. This article argues that the textbook literature constitutes an incredibly rich data source for the historian of economics. In doing so, it offers illustrations from the treatment of the Coase theorem in the textbooks, with a view both to showing how the textbook literature enhances our understanding of the diffusion of economic ideas and how attempts by authors to grapple with new ideas in the context of the textbook literature can result in divergences between how these ideas are treated in the scholarly and textbook literatures.


Author(s):  
Chen-Mao Liao ◽  
Chih-Ming Lin

The objective of the study was to explore the dynamic effects of socioeconomic status (SES) and lifestyle behaviors on the risks of metabolic syndrome (MS) or cardiovascular disease (CVD) in life course. The data of 12,825 subjects (6616 males and 6209 females) who underwent repeated examinations and answered repeated questionnaires from 2006 to 2014 at the Major Health Screening Center in Taiwan, was collected and analyzed. The trajectory of trends in the subjects’ SES and lifestyle mobility over time was observed, and the effects of factors with potential impacts on health were tested and analyzed using multiple logistic regression and a generalized estimated equation model. A 10% increase in MS prevalence was observed over the nine-year period. The average Framingham CVD score for people with MS was estimated to be about 1.4% (SD = 1.5%). Except for middle-aged women, marriage was found to raise the risk of CVD, whereas increasing education and work promotions independently reduced CVD risk for the majority of subjects. However, the risk of CVD was raised by half for young men who had a job or lost a job in comparison to continuously unemployed young men. Physical activity was only found to be advantageous for disease prevention in those aged less than 40 years; increased exercise levels were useless for reducing CVD risk among older men. Alcohol drinking and betel chewing caused increased CVD risk in the old and young subjects, respectively, whereas vegetarian diets and vitamin C/E intake were helpful in preventing CVD, even if those habits were ceased in later life. For middle-aged women, getting sufficient sleep reduced CVD risk. We concluded that SES and lifestyle behaviors may have different effects on health over time, among various populations. Accordingly, suggestions can be provided to healthcare workers in designing health promotion courses for people at different life stages.


2021 ◽  
Vol 58 (3) ◽  
Author(s):  
Torbjörn Bildtgård ◽  
Marianne Winqvist ◽  
Peter Öberg

The increasing prevalence of ageing stepfamilies and the potential of stepchildren to act as a source of support for older parents have increased the interest in long-term intergenerational step relationships. Applying a life-course perspective combined with Simmel’s theorizing on social dynamics, this exploratory study aims to investigate the preconditions for cohesion in long-term intergenerational step relationships. The study is based on interviews with 13 older parents, aged 66–79, who have raised both biological children and stepchildren. Retrospective life-course interviews were used to capture the development of step relationships over time. Interviews were analysed following the principles of analytical induction. The results reveal four central third-party relationships that are important for cohesion in intergenerational step relationships over time, involving: (1) the intimate partner; (2) the non-residential parent; (3) the bridge child; and (4) the stepchild-in-law. The findings have led to the conclusion that if we are to understand the unique conditions for cohesion in long-term intergenerational step relationships, we cannot simply compare biological parent–child dyads with step dyads, because the step relationship is essentially a mediated relationship.


Author(s):  
Christian Olalla-Soler ◽  
Javier Franco Aixelá ◽  
Sara Rovira-Esteva

This article identifies the specific characteristics of Cognitive Translation and Interpreting Studies (CTIS) as a branch of Translation and Interpreting Studies (TIS), adopting a bibliometric approach. The main data source for this study was the Bibliography of Interpreting and Translation (BITRA), which – as at September 2019 – included more than 77,000 TIS records, covering the diversity of languages and document types used in TIS research. BTRA is the only TIS database to feature citing information. CTIS-related records were analysed, and those published between 1976 and 2015 were compared with the whole corpus of TIS research output for the same period – again, as registered in BITRA. Specifically, we analysed: (a) the general features and evolution of CTIS publications over time (by thematic co-occurrence, by title content words, by format and by language); (b) authorship, focusing on co-authorship and on the most productive authors; (c) the citation patterns of CTIS documents, including a brief analysis of its most cited authors and publications; and (d) CTIS accessibility through a study of the ratio of documents published in open access. These aspects were analysed both synchronically and diachronically so as to describe CTIS as a whole and to identify any changes over time. Our results yield a first overview of CTIS from a bibliometric perspective and provide a methodological point of departure for future bibliometric studies in this area.


2021 ◽  
Vol 42 (1) ◽  
pp. 66-80
Author(s):  
Emily Wentzell

People may seek to embody cultural ideals of the life course through their use or rejection of medical interventions, including but not limited to anti-aging treatments. Here, I analyze this phenomenon via interviews with men engaging with two different forms of sexual health medicine in urban Mexico: erectile-dysfunction treatment and testing for sexually transmitted infections (STIs). I argue that, in contrast to the biomedical understanding of patients as individuals who change during their lives, my interlocutors understood themselves as components in broader “collective biologies” that change on a longer timeline. These are culturally-defined groups that people understand to be comprised of interrelated members whose behaviors concretely affect the group’s physical and social well-being over time. In both medical arenas discussed here, men used or rejected sexual health interventions in response to local narratives about the nature of the Mexican population as a collective biology, including ideas about how it should change over time away from its roots in the colonial past. They characterized predispositions to machismo and disinterest in preventative health care as embodied inheritances that the Mexican population should reject in order to achieve health-promoting modernity in the future. My analysis describes how these interlocutors sought to live out desirably modern forms of race and gender through their medical decisions in a way that they hoped would contribute to positive, embodied change in the Mexican social body over time. These findings show that, despite the assumptions of individualism generally naturalized in anti-aging treatment and biomedicine, people may make medical decisions in an effort to aid collective change over population-level timescales.


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