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Public sector health analytics capacity before and after Covid-19: A case study of manager perspectives in New Brunswick, Canada Covid-19 前后公共部门的卫生分析能力:加拿大新不伦瑞克省管理人员视角案例研究
Pub Date : 2024-07-22 DOI: 10.23889/ijpds.v9i1.2370
James Ayles, Maria Lima, Neeru Gupta
BackgroundDemand for health data and analytics to support research, policy, and practice continues to rise, accelerated by the Covid-19 pandemic. Despite the importance of the government analytics workforce in driving academic-based data sharing and linkage platforms, little is known about how public sector managers assess capacity in health analytics. This case study describes findings from consultations among middle managers of analytics services in a Canadian provincial health ministry.MethodsData collection involved a mixed-questions survey to gauge the functional perspective of managers on organisational and human resource analytics capacity within the New Brunswick Department of Health. The repeated cross-sectional survey was implemented in two rounds, with a baseline collected before the Covid-19 global outbreak (in 2016) and a follow-up after the pandemic emergency response (in 2022).ResultsThe post-pandemic period was associated with perceptions of a growing role for public service personnel in handling analytics. Recruitment and retention of skilled analytics professionals emerged as the top priority for capacity building, including needs-based planning, competitive compensation packages to address skills shortages, professional development and promotion opportunities, and tracking key performance indicators for employee satisfaction.ConclusionsGovernment health analytics professionals play a critical role in advancing administrative data use and re-use. Enhanced knowledge sharing is needed on best practices in supply--demand monitoring for analytics professionals and planning for human resources surge capacity in the public service, lest significant innovation potential for health system improvement be left untapped.
背景由于 Covid-19 大流行,对支持研究、政策和实践的健康数据和分析的需求持续上升。尽管政府分析人员在推动基于学术的数据共享和链接平台方面非常重要,但人们对公共部门管理人员如何评估健康分析能力却知之甚少。本案例研究描述了加拿大某省卫生部分析服务中层管理人员的咨询结果。方法数据收集包括一项混合问题调查,以衡量管理人员对新不伦瑞克省卫生部组织和人力资源分析能力的职能观点。重复横断面调查分两轮进行,在 Covid-19 全球疫情爆发前(2016 年)收集基线数据,在大流行应急响应后(2022 年)进行跟踪调查。招聘和留住熟练的分析专业人员成为能力建设的重中之重,包括基于需求的规划、解决技能短缺问题的有竞争力的薪酬方案、职业发展和晋升机会,以及跟踪员工满意度的关键绩效指标。需要加强分析专业人员供需监测和公共服务人力资源激增能力规划方面最佳实践的知识共享,以免卫生系统改进的巨大创新潜力得不到开发。
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引用次数: 0
Data resource profile: Scottish Linked Pregnancy and Baby Dataset (SLiPBD) 数据资源简介:苏格兰关联妊娠和婴儿数据集 (SLiPBD)
Pub Date : 2024-07-18 DOI: 10.23889/ijpds.v9i2.2390
Laura Lindsay, Kate Mark, Emily Moore, J. Carruthers, L. Hopkins, Denise Jennings, R. Wood
IntroductionHere we present the Scottish Linked Pregnancy and Baby Dataset (SLiPBD), a new national data resource held by Public Health Scotland (PHS).MethodsSLiPBD comprises a population-based e-cohort of all fetuses and births (babies) from pregnancies to women in Scotland from 2000 onwards. It is updated monthly by linking and reconciling the following national datasets: antenatal booking records; general and maternity hospital discharge records; termination of pregnancy notifications; and statutory live and stillbirth registrations.ResultsKey information included on all babies in SLiPBD includes estimated date of conception, end of pregnancy date, gestation, multiple pregnancy status, pregnancy outcome, and maternal sociodemographic characteristics. For live births, additional information on the birth, the baby's sociodemographic characteristics, and subsequent infant deaths is included.Following the cohort refresh in January 2024, SLiPBD contained 1,770,226 babies from 1,750,830 pregnancies to 898,161 women. Of the 1,770,226 babies, 1,284,461 (73%) were live births, 5,731 (0.3%) stillbirths, and 316,897 (18%) and 114,840 (6%) came from a pregnancy ending a termination or early spontaneous loss respectively. 22,414 (1%) had an unknown pregnancy outcome, and for 25,883 (1%) the pregnancy was still ongoing. Data completeness for key sociodemographic characteristics except for ethnicity was very high, and variables showed expected patterns. Ethnicity data completeness is poor on historical records but improving over time. Completeness of unique patient identifiers was very high. External validation to source datasets was reassuring.ConclusionSLiPBD can be analysed standalone or linked to other national vital event and health datasets held by PHS. It supports longitudinal and intergenerational analyses, enabling epidemiological and health service surveillance and research on maternal and child health. Researchers interested in accessing pseudonymised extracts of SLiPBD through the Scottish NHS safe haven facility should contact Research Data Scotland. PHS will continue to refine SLiPBD as source datasets improve.Key FeaturesThe Scottish Linked Pregnancy and Baby Dataset (SLiPBD) is a new national data resource created and maintained by Public Health Scotland to facilitate epidemiological and health service analyses focused on maternal and child health.SLiPBD comprises a population-based e-cohort of all fetuses and births (babies) from pregnancies to women in Scotland from 2000 onwards. At least 68,000 babies (of which at least 46,000 are live births) are included annually.SLiPBD is updated on a monthly basis by linking and reconciling records relating to ongoing and completed pregnancies from the following existing national datasets: antenatal booking records; general and maternity hospital discharge records; termination of pregnancy notifications; and statutory live and stillbirth registrations.Key information included on all babies in
导言我们在此介绍苏格兰关联妊娠和婴儿数据集(SLiPBD),这是苏格兰公共卫生部(PHS)掌握的一种新的全国性数据资源。方法SLiPBD 由一个基于人口的电子队列组成,包含 2000 年以来苏格兰妇女怀孕所产生的所有胎儿和新生儿(婴儿)。该数据库每月更新一次,将以下国家数据集连接起来并进行核对:产前预约记录、综合医院和妇产医院出院记录、终止妊娠通知、法定活产和死产登记。结果SLiPBD中所有婴儿的关键信息包括受孕估计日期、妊娠结束日期、妊娠期、多胎妊娠状态、妊娠结果和产妇社会人口特征。在 2024 年 1 月队列刷新后,SLiPBD 共包含 177.0226 万名婴儿,这些婴儿来自 175.083 万名孕妇和 89.8161 万名妇女。在 1,770,226 名婴儿中,1,284,461 名(73%)为活产,5,731 名(0.3%)为死产,316,897 名(18%)和 114,840 名(6%)分别来自终止妊娠或早期自然流产。22,414人(1%)的妊娠结果未知,25,883人(1%)的妊娠仍在进行中。除种族外,其他主要社会人口特征的数据完整性非常高,且变量呈现出预期的模式。在历史记录中,种族数据的完整性较差,但随着时间的推移有所改善。病人唯一标识符的完整性非常高。结论SLiPBD 既可独立分析,也可与 PHS 持有的其他国家人口动态事件和健康数据集链接。它支持纵向和代际分析,有助于流行病学和医疗服务监测以及母婴健康研究。有兴趣通过苏格兰国家医疗服务系统安全避难所设施访问 SLiPBD 化名摘要的研究人员,请联系苏格兰研究数据。主要特点苏格兰关联妊娠和婴儿数据集(SLiPBD)是苏格兰公共卫生部门创建和维护的一个新的全国性数据资源,旨在促进以母婴健康为重点的流行病学和医疗服务分析。SLiPBD 包括一个基于人口的电子队列,包含 2000 年以来苏格兰妇女怀孕所产生的所有胎儿和新生儿(婴儿)。SLiPBD 每月更新一次,将以下现有国家数据集中与正在进行和已完成的妊娠相关的记录连接起来并进行核对:产前预约记录;综合医院和妇产医院出院记录;终止妊娠通知;法定活产和死产登记。SLiPBD中所有婴儿的关键信息包括估计受孕日期、妊娠结束日期、妊娠期、多胎妊娠状态、妊娠结果和产妇社会人口特征。对于活产婴儿,SLiPBD 还包括有关出生、婴儿社会人口特征和任何后续婴儿死亡的附加信息。SLiPBD 中包含医疗服务机构和法定出生登记记录中使用的母亲和婴儿(如适用)的唯一个人标识符,确保 SLiPBD 提供核心的代际脊柱记录,允许在母亲和婴儿之间建立联系,并与其他国家数据集建立联系。经管理部门批准后,研究人员可通过苏格兰公共卫生部门支持的苏格兰国家医疗服务系统安全避难所设施访问 SLiPBD 的化名摘录(根据需要与其他国家数据集链接)。感兴趣的研究人员应向苏格兰研究数据中心 (https://www.researchdata.scot/accessing-data/) 提交初步查询表。
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引用次数: 0
Global trends in prevalence of maternal overweight and obesity: A systematic review and meta-analysis of routinely collected data retrospective cohorts 孕产妇超重和肥胖症患病率的全球趋势:对常规收集数据的回顾性队列进行系统回顾和荟萃分析
Pub Date : 2024-07-15 DOI: 10.23889/ijpds.v9i2.2401
Lisa Kent, Meabh McGirr, K. Eastwood
Pregnant women with obesity are at greater risk of complications during pregnancy, peripartum and post-partum, compared to women with healthy BMI. Worldwide data demonstrating the changes in trends of maternal overweight and obesity prevalence informs service development to address maternal obesity, while directing resources to areas of greatest need. This systematic review and meta-analysis of population level data sought to evaluate global temporal changes in prevalence of maternal obesity and overweight/obesity, and compare trends between regions.Pooled prevalence of obesity and overweight/obesity was estimated using random effects meta-analysis. Temporal and geographical trends in prevalence of obesity and overweight/obesity were examined using linear regression.From 11,684 publications, 94 met inclusion criteria representing 121 study cohorts (Europe n = 71; North America n = 23; Australia/Oceania n = 10; Asia n = 5; South America n = 12), totalling 49,009,168 pregnancies. No studies from Africa met the inclusion criteria. Eighty studies (85.1%) were evaluated as having a low risk of bias and 14 studies (14.9%) moderate. In the most recent full decade (2010-2019), global prevalence of maternal obesity was estimated as 16.3% (95% confidence interval (CI): 15.1-17.5%), or approximately one in six pregnancies. Combined overweight/obesity in pregnancy had a pooled prevalence of 43.8% (95%CI: 42.2-45.4%), approaching half of all pregnancies. In each continent, an upward trend similar to the global trend was observed. North America demonstrated the highest prevalence (obesity: 18.7% (95%CI: 15.0-23.2%)); overweight/obesity: 47.0% (95%CI: 45.7-48.3%)) and Asia demonstrated the lowest prevalence (obesity: 10.8% (95%CI: 7.0-16.5%)); overweight/obesity: 28.5% (95%CI: 18.3-41.5%)). Both maternal obesity and combined overweight/obesity prevalence increased annually by 0.34% and 0.64% (p < 0.001), respectively. Our linear regression model estimates current global prevalence of maternal obesity as 20.9% (95%CI 18.6-23.1%) and projects that this will increase to 23.3% (95%CI 20.3-26.2%) by 2030.Globally, maternal obesity and overweight/obesity prevalence is high and increasing, but varies greatly between regions, being highest in North America and lower in Asia. Maternity services across the globe should be adequately resourced to cope with the complexity of needs of pregnant women living with obesity. Future public health interventions should focus on reversing the high prevalence of maternal obesity observed across the globe. The availability of population-level data and research varies between regions, with more data required to understand the needs of maternal populations in the continents of Africa and Asia. Globally, there is a need for improved harmonisation and publication of data for monitoring and improvement of maternal inequalities.
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引用次数: 0
Maternal disability and newborn discharge to social services: a population-based study 产妇残疾与新生儿接受社会服务:一项基于人口的研究
Pub Date : 2024-07-04 DOI: 10.23889/ijpds.v9i2.2396
Claire Grant, Y. Lunsky, A. Guttmann, Simone Vigod, Isobel Sharpe, K. Fung, Hilary Brown
IntroductionRemoving a child from their family is the option of last resort for social services. However, decisions to place children into care are occurring more frequently and earlier in children's lives, with newborn discharge to social services being a particular concern due to the effects of mother-newborn separations on child development. Women with disabilities face negative assumptions about their parenting capacity, but little is known about their rates of newborn discharge to social services.ObjectivesTo examine the risk of discharge to social services among newborns of women with and without disabilities.MethodsWe conducted a population-based cohort study of singleton livebirths in Ontario, Canada, 2008-2019. We used modified Poisson regression to estimate the relative risk (RR) of discharge to social services immediately after the birth hospital stay, comparing newborns of women with physical (n = 114,685), sensory (n = 38,268), intellectual/developmental (n = 2,094), and multiple disabilities (n = 8,075) to newborns of women without a disability (n = 1,221,765). Within each group, we also examined maternal sociodemographic, health, health care, and pregnancy-related characteristics associated with the outcome.ResultsCompared to newborns of women without disabilities (0.2%), newborns of women with physical (0.5%; aRR 1.53, 95% CI 1.39-1.69), sensory (0.4%; aRR 1.34, 95% CI 1.12-1.59), intellectual/developmental (5.6%; aRR 5.34, 95% CI 4.36-6.53), and multiple disabilities (1.7%; aRR 3.09, 95% CI 2.56-3.72) had increased risk of being discharged to social services after the birth hospital stay. Within each group, the strongest predictors of the outcome were young maternal age, low income quintile, social assistance, maternal mental illness and substance use disorders, inadequate prenatal care, and neonatal morbidity.ConclusionsNewborns of women with disabilities are at increased risk of being discharged to social services after the birth hospital stay. These findings can be used to inform the development of tailored supports for new mothers with disabilities and their infants.
导言:让儿童离开家庭是社会服务部门最后的选择。然而,将儿童送入保育机构的决定在儿童生命中出现的频率越来越高,时间也越来越早,其中新生儿送入社会服务机构尤其令人担忧,因为母婴分离会影响儿童的发育。我们对 2008-2019 年加拿大安大略省的单胎活产婴儿进行了一项基于人群的队列研究。我们使用改良泊松回归法估算了出生住院后立即转入社会服务机构的相对风险 (RR),并将肢体残疾(n = 114,685 例)、感官残疾(n = 38,268 例)、智力/发育残疾(n = 2,094 例)和多重残疾(n = 8,075 例)产妇的新生儿与非残疾产妇的新生儿(n = 1,221,765 例)进行了比较。在每个组别中,我们还研究了与结果相关的产妇社会人口学、健康、医疗保健和妊娠相关特征。结果与无残疾妇女的新生儿(0.2%)相比,有肢体残疾(0.5%;aRR 1.53,95% CI 1.39-1.69)、感官残疾(0.4%;aRR 1.34,95% CI 1.12-1.59)、智力/发育残疾(5.6%;aRR 5.34,95% CI 4.36-6.53)和多重残疾(1.7%;aRR 3.09,95% CI 2.56-3.72)的新生儿在出生住院后被送往社会服务机构的风险增加。在每个组别中,预测结果最强的因素是年轻产妇年龄、低收入五分位数、社会援助、产妇精神疾病和药物使用障碍、产前护理不足以及新生儿发病率。这些发现可用于为残疾新妈妈及其婴儿提供量身定制的支持。
{"title":"Maternal disability and newborn discharge to social services: a population-based study","authors":"Claire Grant, Y. Lunsky, A. Guttmann, Simone Vigod, Isobel Sharpe, K. Fung, Hilary Brown","doi":"10.23889/ijpds.v9i2.2396","DOIUrl":"https://doi.org/10.23889/ijpds.v9i2.2396","url":null,"abstract":"IntroductionRemoving a child from their family is the option of last resort for social services. However, decisions to place children into care are occurring more frequently and earlier in children's lives, with newborn discharge to social services being a particular concern due to the effects of mother-newborn separations on child development. Women with disabilities face negative assumptions about their parenting capacity, but little is known about their rates of newborn discharge to social services.\u0000ObjectivesTo examine the risk of discharge to social services among newborns of women with and without disabilities.\u0000MethodsWe conducted a population-based cohort study of singleton livebirths in Ontario, Canada, 2008-2019. We used modified Poisson regression to estimate the relative risk (RR) of discharge to social services immediately after the birth hospital stay, comparing newborns of women with physical (n = 114,685), sensory (n = 38,268), intellectual/developmental (n = 2,094), and multiple disabilities (n = 8,075) to newborns of women without a disability (n = 1,221,765). Within each group, we also examined maternal sociodemographic, health, health care, and pregnancy-related characteristics associated with the outcome.\u0000ResultsCompared to newborns of women without disabilities (0.2%), newborns of women with physical (0.5%; aRR 1.53, 95% CI 1.39-1.69), sensory (0.4%; aRR 1.34, 95% CI 1.12-1.59), intellectual/developmental (5.6%; aRR 5.34, 95% CI 4.36-6.53), and multiple disabilities (1.7%; aRR 3.09, 95% CI 2.56-3.72) had increased risk of being discharged to social services after the birth hospital stay. Within each group, the strongest predictors of the outcome were young maternal age, low income quintile, social assistance, maternal mental illness and substance use disorders, inadequate prenatal care, and neonatal morbidity.\u0000ConclusionsNewborns of women with disabilities are at increased risk of being discharged to social services after the birth hospital stay. These findings can be used to inform the development of tailored supports for new mothers with disabilities and their infants.","PeriodicalId":507952,"journal":{"name":"International Journal of Population Data Science","volume":" 46","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141678954","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Generating synthetic identifiers to support development and evaluation of data linkage methods 生成合成标识符,支持数据关联方法的开发和评估
Pub Date : 2024-07-01 DOI: 10.23889/ijpds.v9i1.2389
Joseph Lam, Andy Boyd, Robin Linacre, Ruth Blackburn, Katie Harron
IntroductionCareful development and evaluation of data linkage methods is limited by researcher access to personal identifiers. One solution is to generate synthetic identifiers, which do not pose equivalent privacy concerns, but can form a 'gold-standard' linkage algorithm training dataset. Such data could help inform choices about appropriate linkage strategies in different settings.ObjectivesWe aimed to develop and demonstrate a framework for generating synthetic identifier datasets to support development and evaluation of data linkage methods. We evaluated whether replicating associations between attributes and identifiers improved the utility of the synthetic data for assessing linkage error.MethodsWe determined the steps required to generate synthetic identifiers that replicate the properties of real-world data collection. We then generated synthetic versions of a large UK cohort study (the Avon Longitudinal Study of Parents and Children; ALSPAC), according to the quality and completeness of identifiers recorded over several waves of the cohort. We evaluated the utility of the synthetic identifier data in terms of assessing linkage quality (false matches and missed matches).ResultsComparing data from two collection points in ALSPAC, we found within-person disagreement in identifiers (differences in recording due to both natural change and non-valid entries) in 18% of surnames and 12% of forenames. Rates of disagreement varied by maternal age and ethnic group. Synthetic data provided accurate estimates of linkage quality metrics compared with the original data (within 0.13-0.55% for missed matches and 0.00-0.04% for false matches). Incorporating associations between identifier errors and maternal age/ethnicity improved synthetic data utility.ConclusionsWe show that replicating dependencies between attribute values (e.g. ethnicity), values of identifiers (e.g. name), identifier disagreements (e.g. missing values, errors or changes over time), and their patterns and distribution structure enables generation of realistic synthetic data that can be used for robust evaluation of linkage methods.
导言:数据关联方法的仔细开发和评估受到研究人员获取个人识别信息的限制。一种解决方案是生成合成标识符,这种标识符不会带来同等的隐私问题,但可以形成 "黄金标准 "的链接算法训练数据集。我们的目标是开发并演示一个生成合成标识符数据集的框架,以支持数据关联方法的开发和评估。我们评估了复制属性和标识符之间的关联是否能提高合成数据在评估关联错误方面的效用。方法我们确定了生成合成标识符所需的步骤,以复制真实世界数据收集的属性。然后,我们根据英国一项大型队列研究(Avon Longitudinal Study of Parents and Children; ALSPAC)的质量和完整性,生成了该队列研究的合成版本。结果通过比较 ALSPAC 两个收集点的数据,我们发现 18% 的姓氏和 12% 的名字在人内识别符上存在差异(由于自然变化和无效条目造成的记录差异)。不一致率因母亲年龄和种族群体而异。与原始数据相比,合成数据提供了准确的联系质量指标估计值(漏配率在 0.13-0.55% 以内,假配率在 0.00-0.04% 以内)。结论我们的研究表明,复制属性值(如种族)、标识符值(如姓名)、标识符差异(如缺失值、错误或随时间的变化)之间的依赖关系及其模式和分布结构,可以生成真实的合成数据,用于对关联方法进行稳健评估。
{"title":"Generating synthetic identifiers to support development and evaluation of data linkage methods","authors":"Joseph Lam, Andy Boyd, Robin Linacre, Ruth Blackburn, Katie Harron","doi":"10.23889/ijpds.v9i1.2389","DOIUrl":"https://doi.org/10.23889/ijpds.v9i1.2389","url":null,"abstract":"IntroductionCareful development and evaluation of data linkage methods is limited by researcher access to personal identifiers. One solution is to generate synthetic identifiers, which do not pose equivalent privacy concerns, but can form a 'gold-standard' linkage algorithm training dataset. Such data could help inform choices about appropriate linkage strategies in different settings.\u0000ObjectivesWe aimed to develop and demonstrate a framework for generating synthetic identifier datasets to support development and evaluation of data linkage methods. We evaluated whether replicating associations between attributes and identifiers improved the utility of the synthetic data for assessing linkage error.\u0000MethodsWe determined the steps required to generate synthetic identifiers that replicate the properties of real-world data collection. We then generated synthetic versions of a large UK cohort study (the Avon Longitudinal Study of Parents and Children; ALSPAC), according to the quality and completeness of identifiers recorded over several waves of the cohort. We evaluated the utility of the synthetic identifier data in terms of assessing linkage quality (false matches and missed matches).\u0000ResultsComparing data from two collection points in ALSPAC, we found within-person disagreement in identifiers (differences in recording due to both natural change and non-valid entries) in 18% of surnames and 12% of forenames. Rates of disagreement varied by maternal age and ethnic group. Synthetic data provided accurate estimates of linkage quality metrics compared with the original data (within 0.13-0.55% for missed matches and 0.00-0.04% for false matches). Incorporating associations between identifier errors and maternal age/ethnicity improved synthetic data utility.\u0000ConclusionsWe show that replicating dependencies between attribute values (e.g. ethnicity), values of identifiers (e.g. name), identifier disagreements (e.g. missing values, errors or changes over time), and their patterns and distribution structure enables generation of realistic synthetic data that can be used for robust evaluation of linkage methods.","PeriodicalId":507952,"journal":{"name":"International Journal of Population Data Science","volume":"372 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141707970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Understanding Vulnerability to the Poverty Premium: An Analysis of Factors Influencing Use of High-Cost Credit Among Low-Income Individuals 了解贫困溢价的脆弱性:影响低收入个人使用高成本信贷的因素分析
Pub Date : 2024-06-10 DOI: 10.23889/ijpds.v9i4.2431
Fiona Rasanga, Tina Harrison, Raffaella Calabrese
Introduction & BackgroundAccess to affordable credit is essential for individuals living on low incomes to participate in society fully. However, due to their limited credit history and volatile incomes, many cannot access mainstream sources of credit, such as credit cards and personal loans.As a result, they often must rely on more expensive sources of credit such as payday loans, doorstep loans or rent-to-own loans. This leads to them paying more for credit, also referred to as the poverty premium.Incurring the poverty premium exacerbates the financial challenges faced by already vulnerable individuals and can lead to a cycle of financial distress. Identifying the behaviours and factors that lead to a need for high-cost credit can help in identifying individuals who are most vulnerable to incurring the poverty premium.Objectives & ApproachTo achieve this, we rely on anonymized Open Banking transaction data from 100,000 individuals provided by a UK-based social lender.Given the latent nature of vulnerability, we identify indicators of vulnerability to poverty premium which include frequency of overdraft use, previous debt problems, low financial resilience, and indebtedness. We use a copula-based approach to create an index of vulnerability to poverty premium.This is based on weighting the individual indicators using their Spearman rank correlation coefficient. We use a fixed effects model to identify the factors that contribute to this vulnerability, where the index of vulnerability is the dependent variable.Relevance to Digital FootprintsWe use a rich and granular dataset on individual financial transactions to address a key social issue. The findings from this study can inform policy and industry efforts to promote greater credit affordability for these vulnerable individuals. This is particularly important due to the renewed concerns regarding the increased use of high-cost credit by individuals living on low incomes due to COVID-19 and the increased cost of living.ResultsOur findings show that variables related to the financial profile of an individual are important driving factors of the vulnerability to poverty premium. These include the number of salary sources, frequency of salary receipt, benefit receipt and savings frequency. Other variables related to spending behaviour such as gambling, volatility in fixed expenses and high transaction counts all have positive relationships with this vulnerability.Conclusions & ImplicationsThis study is a first step towards examining the determinants of vulnerability to poverty premium by analyzing an Open Banking transaction data set. The innovative feature of this work is the creation of an index of vulnerability to poverty premiums based on various indicators of financial distress and high-cost credit use.Our findings on the relationships between the individual's financial profile and the vulnerability to poverty premium suggest that policymakers should consider targeting interventions fo
简介和背景获得可负担得起的信贷对低收入者充分参与社会生活至关重要。然而,由于他们的信用记录有限且收入不稳定,许多人无法获得信用卡和个人贷款等主流信贷来源。因此,他们往往必须依赖发薪日贷款、上门贷款或租房贷款等更昂贵的信贷来源。贫困溢价加剧了本已脆弱的个人所面临的财务挑战,并可能导致财务困境的恶性循环。识别导致需要高成本信贷的行为和因素有助于识别最容易产生贫困溢价的个人。为了实现这一目标,我们依靠一家英国社会贷款机构提供的 10 万名个人的匿名开放银行交易数据。我们使用基于共轭的方法来创建贫困溢价脆弱性指数,该方法基于使用斯皮尔曼等级相关系数对各个指标进行加权。我们使用固定效应模型来确定导致这种脆弱性的因素,其中脆弱性指数是因变量。与数字足迹的相关性我们使用丰富而精细的个人金融交易数据集来解决一个关键的社会问题。这项研究的结果可以为政策和行业提供参考,从而提高这些弱势群体的信贷负担能力。结果我们的研究结果表明,与个人财务状况相关的变量是导致易陷入贫困溢价的重要驱动因素。这些变量包括工资来源的数量、领取工资的频率、领取福利和储蓄的频率。其他与消费行为有关的变量,如赌博、固定支出的波动性和高交易次数,都与这种脆弱性有正相关关系。 结论与启示 这项研究是通过分析开放银行交易数据集来研究贫困溢价脆弱性决定因素的第一步。这项工作的创新之处在于根据财务困境和高成本信贷使用的各种指标创建了易受贫困溢价影响的指数。我们关于个人财务状况与易受贫困溢价影响之间关系的研究结果表明,政策制定者应考虑针对具有特定特征的个人采取干预措施,以减少对高成本信贷的需求。例如,针对赌博者和消费行为不稳定者的定期储蓄或理财教育计划,可以帮助这些人更好地管理自己的财务。
{"title":"Understanding Vulnerability to the Poverty Premium: An Analysis of Factors Influencing Use of High-Cost Credit Among Low-Income Individuals","authors":"Fiona Rasanga, Tina Harrison, Raffaella Calabrese","doi":"10.23889/ijpds.v9i4.2431","DOIUrl":"https://doi.org/10.23889/ijpds.v9i4.2431","url":null,"abstract":"Introduction & BackgroundAccess to affordable credit is essential for individuals living on low incomes to participate in society fully. However, due to their limited credit history and volatile incomes, many cannot access mainstream sources of credit, such as credit cards and personal loans.\u0000As a result, they often must rely on more expensive sources of credit such as payday loans, doorstep loans or rent-to-own loans. This leads to them paying more for credit, also referred to as the poverty premium.\u0000Incurring the poverty premium exacerbates the financial challenges faced by already vulnerable individuals and can lead to a cycle of financial distress. Identifying the behaviours and factors that lead to a need for high-cost credit can help in identifying individuals who are most vulnerable to incurring the poverty premium.\u0000Objectives & ApproachTo achieve this, we rely on anonymized Open Banking transaction data from 100,000 individuals provided by a UK-based social lender.Given the latent nature of vulnerability, we identify indicators of vulnerability to poverty premium which include frequency of overdraft use, previous debt problems, low financial resilience, and indebtedness. We use a copula-based approach to create an index of vulnerability to poverty premium.\u0000This is based on weighting the individual indicators using their Spearman rank correlation coefficient. We use a fixed effects model to identify the factors that contribute to this vulnerability, where the index of vulnerability is the dependent variable.\u0000Relevance to Digital FootprintsWe use a rich and granular dataset on individual financial transactions to address a key social issue. The findings from this study can inform policy and industry efforts to promote greater credit affordability for these vulnerable individuals. This is particularly important due to the renewed concerns regarding the increased use of high-cost credit by individuals living on low incomes due to COVID-19 and the increased cost of living.\u0000ResultsOur findings show that variables related to the financial profile of an individual are important driving factors of the vulnerability to poverty premium. These include the number of salary sources, frequency of salary receipt, benefit receipt and savings frequency. Other variables related to spending behaviour such as gambling, volatility in fixed expenses and high transaction counts all have positive relationships with this vulnerability.\u0000Conclusions & ImplicationsThis study is a first step towards examining the determinants of vulnerability to poverty premium by analyzing an Open Banking transaction data set. The innovative feature of this work is the creation of an index of vulnerability to poverty premiums based on various indicators of financial distress and high-cost credit use.\u0000Our findings on the relationships between the individual's financial profile and the vulnerability to poverty premium suggest that policymakers should consider targeting interventions fo","PeriodicalId":507952,"journal":{"name":"International Journal of Population Data Science","volume":"104 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141361308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Exploring Digital Biomarkers for Depression Using Mobile Technology 利用移动技术探索抑郁症的数字生物标志物
Pub Date : 2024-06-10 DOI: 10.23889/ijpds.v9i4.2422
Yuezhou Zhang, A. Folarin, R. Dobson
Introduction & BackgroundWith the advent of ubiquitous sensors and mobile technologies, wearables and smartphones offer a cost-effective means for monitoring mental health conditions, particularly depression. These devices enable the continuous collection of behavioral data, providing novel insights into the daily manifestations of depressive symptoms. Objectives & ApproachThe present study summarizes findings from our five recent investigations that explored the relationships between depression severity and digital biomarkers captured by wearables and smartphones. These studies analyzed data from RADAR-MDD, a multinational mobile health program, involving 623 participants and tracked for up to two years. Participants' depression severity was measured biweekly using the PHQ-8 questionnaire conducted via smartphones. Concurrently, participants’ Fitbit and smartphone data were also collected. Given the longitudinal nature and repeated measurements for each participant, multilevel modeling techniques were employed to analyze the data. Relevance to Digital FootprintsOur approach involved extracting features from passive data that reflect various aspects of daily behavior—such as sleep quality, social interaction, physical activity, and walking patterns—akin to digital footprints. ResultsWe found several significant links between depression severity and various behavioral biomarkers: elevated depression levels were associated with diminished sleep quality (assessed through Fitbit metrics), reduced sociability (approximated by Bluetooth), decreased levels of physical activity (quantified by step counts and GPS data), a slower cadence of daily walking (captured by smartphone accelerometers), and disturbances in circadian rhythms (analyzed across various data streams). Conclusions & ImplicationsLeveraging digital biomarkers for assessing and continuously monitoring depression introduces a new paradigm in early detection and development of customized intervention strategies. Findings from these studies not only enhance our comprehension of depression in real-world settings but also underscore the potential of mobile technologies in the prevention and management of mental health issues.
简介与背景随着无处不在的传感器和移动技术的出现,可穿戴设备和智能手机为监测心理健康状况,尤其是抑郁症提供了一种经济有效的方法。这些设备可持续收集行为数据,为了解抑郁症状的日常表现提供新的视角。本研究总结了我们最近五项调查的结果,这些调查探讨了抑郁症严重程度与可穿戴设备和智能手机捕获的数字生物标志物之间的关系。这些研究分析了来自跨国移动健康项目 RADAR-MDD 的数据,共有 623 名参与者参与,追踪时间长达两年。参与者的抑郁严重程度每两周通过智能手机使用 PHQ-8 问卷进行一次测量。同时,还收集了参与者的 Fitbit 和智能手机数据。鉴于每位参与者的纵向性质和重复测量,我们采用了多层次建模技术来分析数据。与数字足迹的相关性我们的方法是从被动数据中提取反映日常行为各个方面的特征,如睡眠质量、社交互动、体力活动和步行模式,这与数字足迹类似。结果我们发现抑郁症严重程度与各种行为生物标志物之间存在若干重要联系:抑郁症水平升高与睡眠质量下降(通过 Fitbit 指标评估)、社交能力降低(通过蓝牙近似)、体力活动水平下降(通过步数和 GPS 数据量化)、日常步行节奏减慢(通过智能手机加速度计捕捉)以及昼夜节律紊乱(通过各种数据流分析)有关。结论与启示利用数字生物标志物评估和持续监测抑郁症为早期检测和制定个性化干预策略引入了一种新的模式。这些研究结果不仅增强了我们对真实世界环境中抑郁症的理解,还凸显了移动技术在预防和管理心理健康问题方面的潜力。
{"title":"Exploring Digital Biomarkers for Depression Using Mobile Technology","authors":"Yuezhou Zhang, A. Folarin, R. Dobson","doi":"10.23889/ijpds.v9i4.2422","DOIUrl":"https://doi.org/10.23889/ijpds.v9i4.2422","url":null,"abstract":"Introduction & BackgroundWith the advent of ubiquitous sensors and mobile technologies, wearables and smartphones offer a cost-effective means for monitoring mental health conditions, particularly depression. These devices enable the continuous collection of behavioral data, providing novel insights into the daily manifestations of depressive symptoms. \u0000Objectives & ApproachThe present study summarizes findings from our five recent investigations that explored the relationships between depression severity and digital biomarkers captured by wearables and smartphones. These studies analyzed data from RADAR-MDD, a multinational mobile health program, involving 623 participants and tracked for up to two years. Participants' depression severity was measured biweekly using the PHQ-8 questionnaire conducted via smartphones. Concurrently, participants’ Fitbit and smartphone data were also collected. Given the longitudinal nature and repeated measurements for each participant, multilevel modeling techniques were employed to analyze the data. \u0000Relevance to Digital FootprintsOur approach involved extracting features from passive data that reflect various aspects of daily behavior—such as sleep quality, social interaction, physical activity, and walking patterns—akin to digital footprints. \u0000ResultsWe found several significant links between depression severity and various behavioral biomarkers: elevated depression levels were associated with diminished sleep quality (assessed through Fitbit metrics), reduced sociability (approximated by Bluetooth), decreased levels of physical activity (quantified by step counts and GPS data), a slower cadence of daily walking (captured by smartphone accelerometers), and disturbances in circadian rhythms (analyzed across various data streams). \u0000Conclusions & ImplicationsLeveraging digital biomarkers for assessing and continuously monitoring depression introduces a new paradigm in early detection and development of customized intervention strategies. Findings from these studies not only enhance our comprehension of depression in real-world settings but also underscore the potential of mobile technologies in the prevention and management of mental health issues.","PeriodicalId":507952,"journal":{"name":"International Journal of Population Data Science","volume":" 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141363886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Utilising User Data from a Food-Sharing App to Evidence the "Heat-or-Eat" Dilemma 利用食品共享应用程序的用户数据来证明 "要么加热,要么吃饭 "的两难选择
Pub Date : 2024-06-10 DOI: 10.23889/ijpds.v9i4.2424
T. Semple, John Harvey, Lucelia Rodrigues, M. Gillott, Grazziela Figueredo, Georgiana Nica-Avram
Introduction & BackgroundPrevious literature has found that financially vulnerable households often make involuntary spending trade-offs between necessities, particularly energy and food. This effect is especially pronounced during winter, when homes require greater energy expenditure to maintain an adequate temperature. Despite frequent colloquial and journalistic references to the "heat-or-eat dilemma”, there remains limited recent empirical evidence of this phenomenon in the UK. This is a considerable knowledge gap, given recent economic hardship and rising energy costs. Objectives & ApproachThis study uses survey data (n=2877), collected during winter 2022 in London, UK, to analyse the sociodemographic and behavioural characteristics of respondents affecting self-reported heat-or-eat trade-offs. The survey was deployed via users of the food-sharing app, OLIO, and quota restraints were enforced to ensure the socioeconomic representativeness of the sample (based on Index of Multiple Deprivation). The survey question of interest (i.e., the dependent variable) was ""in the past year, how frequently did your household reduce or forego expenses for basic household necessities, such as medicine or food, in order to pay an energy bill?"" and responses were recorded using a discrete, ordinal scale: never; 1-2 months; some months but not every month; almost every month. Given the nature of the dependent variable, the Random Parameters Ordered Probit (RPOP) model, a statistical modelling framework used in the case of discrete, ordered outcomes, was considered suitable. The RPOP approach allows the effect of various independent variables to be explored, which in this case, are sociodemographic and behavioural characteristics of respondents. Relevance to Digital FootprintsThe relevance to the digital footprints theme is embedded in the study’s aim: to draw insights into social issues through the analysis of sociodemographic and behavioural data retrieved from the users of a mobile app. ResultsInitial results show that a considerable proportion (~37%) of the sample made heat-or-eat trade-offs at least one month of the year. Interestingly, this is several times higher than the official rate of fuel poverty in London (11.9%), suggesting that the government’s fuel poverty metric fails to capture many homes that display signs of energy unaffordability. The RPOP model estimation results show that a broad range of sociodemographic variables (including features of household composition and disability), as well as several behavioural features derived from the respondents’ use of the OLIO app, including the frequency of app usage and food requests, significantly affected the likelihood of heat-or-eat trade-offs. Conclusions & ImplicationsOur results can be used to guide remedial food and fuel poverty policies. It may be particularly useful to focus on the sociodemographic variables that lead to heat-or-eat trade-offs, given that the English fuel poverty metric
导言与背景以往的文献发现,经济上处于弱势的家庭往往会在必需品(尤其是能源和食品)之间做出非自愿的支出权衡。这种影响在冬季尤为明显,因为冬季家庭需要消耗更多的能源来维持适当的温度。尽管口语和新闻报道中经常提到 "要么取暖,要么吃饭的两难境地",但最近在英国有关这一现象的经验证据仍然有限。考虑到近期的经济困难和不断上涨的能源成本,这是一个相当大的知识空白。目标与方法 本研究使用 2022 年冬季在英国伦敦收集的调查数据(n=2877),分析受访者的社会人口和行为特征对自我报告的 "热或吃 "权衡的影响。调查是通过食物共享应用 OLIO 的用户进行的,并实施了配额限制,以确保样本的社会经济代表性(基于多重贫困指数)。相关调查问题(即因变量)为""在过去一年中,您的家庭为了支付能源账单而减少或放弃家庭基本必需品(如药品或食品)开支的频率如何?鉴于因变量的性质,随机参数有序 Probit(RPOP)模型被认为是合适的,该模型是一种用于离散、有序结果的统计建模框架。RPOP 方法允许探讨各种自变量的影响,在本案例中,这些自变量是受访者的社会人口和行为特征。与 "数字足迹 "的相关性与 "数字足迹 "主题的相关性体现在本研究的目的上:通过分析从移动应用程序用户那里获取的社会人口和行为数据,深入了解社会问题。结果初步结果显示,相当大比例的样本(约 37%)在一年中至少有一个月做出了 "吃或热 "的权衡。有趣的是,这一比例比伦敦官方公布的燃料贫困率(11.9%)高出数倍,这表明政府的燃料贫困指标未能反映出许多显示出能源负担不起迹象的家庭。RPOP 模型的估算结果表明,一系列社会人口变量(包括家庭组成和残疾特征),以及受访者使用 OLIO 应用程序时的一些行为特征(包括使用应用程序的频率和食物请求),都对取暖或就餐权衡的可能性产生了显著影响。结论与启示我们的研究结果可用于指导粮食和燃料贫困的补救政策。鉴于英国的燃料贫困衡量标准将重点放在家庭的能源效率而不是居住者的特征上,因此关注导致 "热或吃 "权衡的社会人口变量可能特别有用。
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引用次数: 0
Who donates food purchase data for research? Results from two nationwide data collection efforts in Finland 谁捐赠食品购买数据用于研究?芬兰两次全国性数据收集工作的结果
Pub Date : 2024-06-10 DOI: 10.23889/ijpds.v9i4.2428
Anna-Leena Vuorinen, H. Vepsäläinen, Jelena Meinilä, E. Lehto, H. Saarijärvi, M. Erkkola, Mikael Fogelholm, J. Nevalainen
Introduction & BackgroundFood retailers’ transaction data are increasingly used for research. Unlike many other digital footprints, the representativeness of automatically accumulating food purchase data as such is less biased as food is consumed by all individuals. However, the process of obtaining individual/household level data requires consents from the consumers and, thus, may create selection bias. Objectives & ApproachThe aim of this work is to describe the recruitment process and participant characteristics in the Finnish LoCard study to evaluate the selection mechanism. The Finnish LoCard study comprises two cohorts collected in 2018 and 2023 with 47,066 and 42,340 participants, respectively, who have consented to release their food purchase data for research. The study collaborates with S group, the leading retailer in Finland with 47% market share. Members from their loyalty card program were invited to consent to their purchase data being used for research and voluntarily respond to a background questionnaire. Relevance to Digital FootprintsOur analyses may provide further insights into the selectivity of consumers who are willing to share their purchase data for research purposes. ResultsFor both LoCard cohorts, all loyalty card holders (n~2.3M) were considered. In LoCard I, the invitations were sent to 1.1M primary card holders with confirmed email addresses, of whom 47,066 (3.9%) participated and consented to their purchase data being used for research. In this cohort, women, middle-aged individuals, individuals with higher education, and employed individuals were overrepresented whereas the retired individuals, those with lower education and individuals with children were underrepresented. In the LoCard II, loyalty card holders (n ~2.24M) with an email address were invited. Of these, 852,009 (37.7%) opened the invitation link, and a further 42,340 provided the consent, resulting in response rate of 1.9% from the original population and 4.9% from those reacting to the email invitation. Data on the characteristics of LoCard II participants are not available yet but will be presented in the conference presentation. Conclusions & ImplicationsThis work investigates selection mechanisms in the Finnish LoCard study and evaluates the feasibility of reaching underrepresented groups in health studies, such as socioeconomically disadvantaged groups or young men, through a combination of loyalty card program and email invitations.
简介与背景食品零售商的交易数据越来越多地被用于研究。与许多其他数字足迹不同,自动积累的食品购买数据的代表性较低,因为食品是由所有人消费的。不过,获取个人/家庭层面数据的过程需要征得消费者的同意,因此可能会产生选择偏差。目标与方法 本研究旨在描述芬兰 "购物卡 "研究的招募过程和参与者特征,以评估选择机制。芬兰 "乐卡 "研究包括 2018 年和 2023 年收集的两个队列,分别有 47066 名和 42340 名参与者同意将其食品购买数据用于研究。该研究与芬兰领先的零售商 S 集团合作,后者拥有 47% 的市场份额。S集团邀请其会员卡计划的会员同意将其购买数据用于研究,并自愿回答背景调查问卷。与数字足迹的相关性我们的分析可以进一步揭示愿意为研究目的分享其购买数据的消费者的选择性。结果在两批 LoCard 中,所有会员卡持有者(230 万)都被考虑在内。在 LoCard I 中,邀请函发送给了 110 万名拥有确认电子邮件地址的主卡持有者,其中 47,066 人(3.9%)参与并同意将其购买数据用于研究。在这一群体中,女性、中年人、受过高等教育的人和在职人员所占比例较高,而退休人员、受教育程度较低的人和有子女的人所占比例较低。LoCard II 邀请了拥有电子邮件地址的会员卡持有者(n ~224万)。其中 852 009 人(37.7%)打开了邀请链接,另有 42 340 人提供了同意书,因此原始人群的回复率为 1.9%,对电子邮件邀请做出反应的人群的回复率为 4.9%。有关 LoCard II 参与者特征的数据尚未公布,但将在会议发言中介绍。结论与启示这项研究调查了芬兰 "乐卡 "研究中的选择机制,并评估了通过会员卡计划和电子邮件邀请相结合的方式接触健康研究中代表性不足的群体(如社会经济弱势群体或年轻男性)的可行性。
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引用次数: 0
The role of inequalities in managing symptoms of menstruation: harnessing shopping data to innovate female reproductive health research 月经症状管理中的不平等现象:利用购物数据创新女性生殖健康研究
Pub Date : 2024-06-10 DOI: 10.23889/ijpds.v9i4.2416
Poppy Taylor, A. Skatova, Laura D Howe, Abigail Fraser, Hannah Knight
Introduction & BackgroundMenstruation affects half the population, yet its patterns and management are greatly under-researched. A regular and functioning menstrual cycle is considered an important vital sign and menstrual-related issues can be strong indicators of both reproductive and wider health issues. This project explores a novel health data source - shopping data history - to study how individuals manage menstrual symptoms such as pain, intensity of flow, mental health, and other issues, and explore potential social inequalities in these management strategies. Objectives & ApproachWe present a conceptual framework of studying management of menstruation symptoms using shopping data. The core objectives of this research are to enhance our understanding of menstrual management strategies and potential inequalities in these whilst evaluating the utility and acceptability of shopping data for future female reproductive health research. Our research will focus on harnessing loyalty card data from UK supermarkets and pharmaceutical retailers to provide insights into the management of menstrual symptoms at a national level. We will study retail data to identify products and patterns of purchasing which may be relevant to menstrual management and conduct surveys for linkage with shopping data. The public will be consulted to investigate attitudes towards shopping data for health research and inform interpretations of patterns in the data. Relevance to Digital FootprintsThis project contributes to advancing of understanding of using digital data for health research on an important societal challenge. We investigate the practical applications for menstrual health and other female reproductive health issues, with scope to enact meaningful change. Conclusions & ImplicationsBy analysing shopping behaviour, combined with survey data and area-level socioeconomic data, we aim to identify regions of the UK and individual characteristics which influence the risk of experiencing menstrual symptoms and ability to manage these within a high-income context. Our research will contribute to understanding of menstrual management strategies for women and people who menstruate, and associated inequalities.
导言与背景月经影响着半数人口,但对其模式和管理的研究却远远不够。规律而正常的月经周期被认为是重要的生命体征,与月经相关的问题是生殖健康和更广泛健康问题的有力指标。本项目利用新颖的健康数据源--购物数据历史记录--研究个人如何管理痛经、经量强度、心理健康等月经症状,并探索这些管理策略中潜在的社会不平等。目标与方法我们提出了一个利用购物数据研究月经症状管理的概念框架。本研究的核心目标是加强我们对月经管理策略和其中潜在不平等现象的了解,同时评估购物数据在未来女性生殖健康研究中的实用性和可接受性。我们的研究重点是利用英国超市和药品零售商的会员卡数据,深入了解全国范围内的月经症状管理情况。我们将研究零售数据,以确定可能与月经管理相关的产品和购买模式,并进行调查,以便与购物数据建立联系。我们将咨询公众,调查他们对用于健康研究的购物数据的态度,并为解释数据中的模式提供信息。与 "数字足迹 "的相关性该项目有助于加深对将数字数据用于健康研究这一重要社会挑战的理解。我们对月经健康和其他女性生殖健康问题的实际应用进行了调查,以期实现有意义的变革。结论与影响通过分析购物行为,结合调查数据和地区级社会经济数据,我们旨在确定英国的哪些地区和个人特征会影响月经症状的发生风险,以及在高收入背景下控制这些症状的能力。我们的研究将有助于了解妇女和月经患者的月经管理策略以及相关的不平等现象。
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引用次数: 0
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International Journal of Population Data Science
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