scholarly journals Assessing and Improving the Use of Online Information About Child Development, Education, Health, and Well-Being in Low-Education, Low-Income Parents: Protocol for a Mixed-Methods Multiphase Study (Preprint)

2018 ◽  
Author(s):  
Pierre Pluye ◽  
Christine Loignon ◽  
François Lagarde ◽  
Geneviève Doray ◽  
Reem El Sherif ◽  
...  
Keyword(s):  
Health Outcomes ◽  
Health Information ◽  
Phase 1 ◽  
Well Being ◽  
Low Ses ◽  
Online Information ◽  
Development Education ◽  
High Quality ◽  
Parents And Children ◽  
Health And Well Being

BACKGROUND This study is born from a partnership between Web editors of Naître et grandir (N&G) and AboutKidsHealth (AKH) and researchers who developed and validated the Information Assessment Method (IAM). N&G and AKH are popular Canadian websites with high-quality comprehensive information about child development, education, health, and well-being. IAM allows parents to assess online information and provide feedback to Web editors. High-quality online consumer health information improves knowledge, self-efficacy, and health. However, low-socioeconomic status (SES) parents underuse N&G and IAM, despite these parents being more likely to report decreased worries and increased confidence as outcomes from N&G information. OBJECTIVE The study is aimed to improve low-SES parents’ use of online child information and interaction with Web editors and explore subsequent health outcomes for parents and children. METHODS Multiphase mixed-methods design. Our general approach is centered on organizational participatory research. In phase 1, we will conduct a qualitative interpretive study to identify barriers and facilitators to using N&G information and to interacting with N&G editors via IAM; interview more than 10 low-SES parents about their experience with N&G and IAM and more than 10 nonusers of N&G and IAM; and use thematic analysis to identify main barriers and facilitators. In phase 2, we will integrate parents’ views (phase 1 findings) in N&G and IAM and implement a new version: IAM+N&G+. In phase 3, we will conduct a quantitative prospective longitudinal study (pre-/postimplementation monitoring of knowledge use and outcomes). We will compare the use of original (IAM and N&G) and new (IAM+ and N&G+) versions using Google Analytics variables, IAM variables, a material and social deprivation index, and demographics. We anticipate increased use post implementation (linear mixed modeling). In phase 4, we will conduct a qualitative descriptive study on outcomes of information use. We will interview more than 30 low-SES parents who receive and rate the N&G+ newsletter using IAM+ and analyze data in the form of life histories to describe how parents and children experience perceived outcomes. RESULTS The project was funded in 2017 by the Canadian Institutes of Health Research and received an ethics approval by the McGill University’s institutional review board. Data collection for phase 1 was completed in 2018. Phases 2 to 4 will be conducted until 2020. Findings from this study will also be used to develop a free toolkit, useful to all Web editors, with recommendations for improving health information for low-SES persons and interactions with them using IAM. CONCLUSIONS The results of this study will provide a deep understanding of how low-SES parents use online child information and interact with Web editors. Following the implementation of IAM+N&G+, results will also elucidate subsequent health outcomes for low-SES parents and children after interaction with Web editors has been optimized. INTERNATIONAL REGISTERED REPOR PRR1-10.2196/9996

scholarly journals Updated systematic review and meta-analysis of studies examining the relationship between reported racism and health and well-being for children and youth: a protocol

BMJ Open ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. e043722
Author(s):  
Naomi Priest ◽  
Kate Doery ◽  
Mandy Truong ◽  
Shuaijun Guo ◽  
Ryan Perry ◽  
...  
Keyword(s):  
Systematic Review ◽  
Health Outcomes ◽  
Research Policy ◽  
Meta Analysis ◽  
Well Being ◽  
Children And Youth ◽  
Effect Sizes ◽  
Future Research ◽  
Critical Determinant ◽  
Health And Well Being

IntroductionRacism is a critical determinant of health and health inequities for children and youth. This protocol aims to update the first systematic review conducted by Priest et al (2013), including a meta-analysis of findings. Based on previous empirical data, it is anticipated that child and youth health will be negatively impacted by racism. Findings from this review will provide updated evidence of effect sizes across outcomes and identify moderators and mediators of relationships between racism and health.Methods and analysisThis systematic review and meta-analysis will include studies that examine associations between experiences of racism and racial discrimination with health outcomes of children and youth aged 0–24 years. Exposure measures include self-reported or proxy reported systemic, interpersonal and intrapersonal racism. Outcome measures include general health and well-being, physical health, mental health, biological markers, healthcare utilisation and health behaviours. A comprehensive search of studies from the earliest time available to October 2020 will be conducted. A random effects meta-analysis will examine the average effect of racism on a range of health outcomes. Study-level moderation will test the difference in effect sizes with regard to various sample and exposure characteristics. This review has been registered with the International Prospective Register of Systematic Reviews.Ethics and disseminationThis review will provide evidence for future research within the field and help to support policy and practice development. Results will be widely disseminated to both academic and non-academic audiences through peer-review publications, community summaries and presentations to research, policy, practice and community audiences.PROSPERO registration numberCRD42020184055.

scholarly journals Association of military life experiences and health indicators among military spouses

2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Nida H. Corry ◽  
Sharmini Radakrishnan ◽  
Christianna S. Williams ◽  
Alicia C. Sparks ◽  
Kelly A. Woodall ◽  
...  
Keyword(s):  
Health Outcomes ◽  
Life Experiences ◽  
Health Indicators ◽  
Well Being ◽  
Healthy People ◽  
Military Spouses ◽  
Healthy Weight ◽  
Military Life ◽  
Healthy People 2020 ◽  
Health And Well Being

Abstract Background The health and well-being of military spouses directly contribute to a robust military force by enabling the spouse to better support the active duty member’s career. In order to understand the overall health and well-being of military spouses, we assessed health indicators among military spouses using the Healthy People 2020 framework and examined associations of these health indicators with military experiences and psychosocial factors. Methods Using data from the Millennium Cohort Family Study, a U.S. Department of Defense-sponsored survey of 9872 spouses of service members with 2–5 years of military service, we examined attainment of Healthy People 2020 goals for spouses and service members, including healthy weight, exercise, sleep, and alcohol and tobacco use. Multivariable logistic regression models assessed associations of spouse health indicators with stressful military life experiences and social support, adjusting for demographics and military descriptors. The spousal survey was administered nationwide in 2011. Results The majority of military spouses met each health goal assessed. However, less than half met the healthy weight and the strength training goals. Reporting greater perceived family support from the military was associated with better behavioral health outcomes, while having no one to turn to for support was associated with poorer outcomes. Using the Healthy People 2020 objectives as a framework for identifying key health behaviors and benchmarks, this study identified factors, including military-specific experiences, that may contribute to physical health behaviors and outcomes among military spouses. With respect to demographic characteristics, the findings are consistent with other literature that women are more likely to refrain from risky substance use and that greater education is associated with better overall health outcomes. Conclusions Findings suggest that enhanced social and military support and tailored programming for military spouses may improve health outcomes and contribute to the well-being of military couples. Such programming could also bolster force readiness and retention.

scholarly journals Family trouble: Heteronormativity, emotion work and queer youth mental health

2019 ◽  
pp. 136345931986057 ◽  
Author(s):  
Elizabeth McDermott ◽  
Jacqui Gabb ◽  
Rachael Eastham ◽  
Ali Hanbury
Keyword(s):  
Mental Health ◽  
Family Relationships ◽  
Phase 1 ◽  
Youth Mental Health ◽  
Well Being ◽  
Emotion Work ◽  
Lgbtq Youth ◽  
Cross Sectional ◽  
Queer Youth ◽  
Health And Well Being

Conflict with the family about sexual orientation and gender diversity is a key risk factor associated with poor mental health in youth populations. Findings presented here derive from a UK study that employed an interdisciplinary critical mental health approach that de-pathologised emotional distress and conceptualised families as social and affective units that are created through everyday practices. Our aim was to explore how family relationships foster, maintain or harm the mental health and well-being of LGBTQ+ youth. Data were generated through exploratory visual, creative and digital qualitative methods in two phases. Phase 1 involved digital/paper emotion maps and interviews with LGBTQ+ youth aged 16 to 25 (n = 12) and family member/mentor interviews (n = 7). Phase 2 employed diary methods and follow-up interviews (n = 9). The data analytic strategy involved three stages: individual case analysis, cross-sectional thematic analysis and meta-interpretation. We found that family relationships impacted queer youth mental health in complex ways that were related to the establishment of their autonomous queer selves, the desire to remain belonging to their family and the need to maintain a secure environment. The emotion work involved in navigating identity, belonging and security was made difficult because of family heteronormativity, youth autonomy and family expectations, and had a stark impact on queer youth mental health and well-being. Improving the mental health of LGBTQ+ youth requires a much deeper understanding of the emotionality of family relationships and the difficulties negotiating these as a young person.

Development of a Translation Standard to support the improvement of health literacy and provide consistent high-quality information

2013 ◽  
Vol 37 (4) ◽  
pp. 547 ◽  
Author(s):  
Jaklina Michael ◽  
Tracy Aylen ◽  
Rajna Ogrin
Keyword(s):  
Health Literacy ◽  
Health Outcomes ◽  
Health Information ◽  
Culturally Relevant ◽  
Healthcare Providers ◽  
Relevant Information ◽  
Consumer Health Information ◽  
Target Audience ◽  
Consumer Health ◽  
High Quality

Australia has a high number of people from culturally and linguistically diverse (CALD) backgrounds whose primary language is not English. CALD population groups have comparatively lower levels of education and health literacy, and poorer health outcomes compared with the Australian-born population. The delivery of consumer health information to people from CALD backgrounds usually includes the use of translated resources. Unfortunately, the quality of translated resources available on health issues is highly variable and may impact efforts to address the disparities in health outcomes. Currently applied guides to translation focus on accuracy and literalness of the translation; however, for health translations, conveying meaning and incorporating culturally relevant information is essential. Minimum standards for developing translated resources are needed to provide an indication of quality for end users, including healthcare providers, the client and carer. This paper describes the development of a Translation Standard, led by a community nursing organisation in collaboration and consultation with CALD community members and peak community organisations in Melbourne, Australia. The Translation Standard includes 10 components that have been identified as necessary to ensure a minimum standard of translation that is of high quality and caters to the health literacy levels of the target audience. What is known about the topic? There are many people from CALD backgrounds who have worse health outcomes than people who are Australian born. There is a gap in guidance to health professionals on how to develop high-quality translations of consumer health information that consider culture and health literacy. Higher-quality translations are needed to better inform CALD groups about their health. What does this paper add? The description of a new Translation Standard to guide the development of culturally relevant consumer health translations, considering the cultural needs and health literacy level of the target audience. What are the implications for practitioners? The Translation Standard provides assurance to practitioners that any translation that has followed this Standard is of high quality and increases the likelihood that the target audience will find the information relevant and understandable. The Translation Standard can assist consumers to make more informed choices and decisions about their health. Future translations would benefit by using such a guide.

Non-religion, atheism, and mental health

2021 ◽  
pp. 259-276
Author(s):  
Miguel Farias ◽  
Thomas J. Coleman III
Keyword(s):  
Mental Health ◽  
Health Risk ◽  
Health Outcomes ◽  
Recent Work ◽  
Religious Experience ◽  
Well Being ◽  
Methodological Issues ◽  
The World ◽  
Methodological Problems ◽  
Health And Well Being

Based on the well-established link between religiosity and positive mental health outcomes, it has been argued that non-religiosity is a health liability. However, most of this research suffers from methodological problems that limit their generalizability to non-religious populations, such as atheists and agnostics. In this chapter, we draw attention to these methodological issues, and argue in favour of a richer conceptualization of non-religion than has been theorized in previous literature. We further review recent work from various countries around the world, which challenges the notion that non-religiosity presents a health risk, finding instead that the non-religious experience similar levels of health and well-being benefits as the religious. We end by briefly discussing the limitations and recent backlash at this literature, while suggesting that the study of the non-religious may transform how we understand the interaction between beliefs, rituals, and health.

A Review and Response to the Early Mental Health and Neurological Consequences of the COVID-19 Pandemic

2021 ◽  
Author(s):  
Lara Beth Aknin ◽  
Jan Emmanuel De Neve ◽  
Elizabeth Warren Dunn ◽  
Daisy Fancourt ◽  
Elkhonon Goldberg ◽  
...  
Keyword(s):  
Mental Health ◽  
Well Being ◽  
Anxiety And Depression ◽  
Social Connection ◽  
Short Term ◽  
Policy And Practice ◽  
High Quality ◽  
Neurological Sequelae ◽  
The Impact ◽  
Health And Well Being

COVID-19 has infected millions of people and upended the lives of most humans on the planet. Researchers from across the psychological sciences have sought to document and investigate the impact of COVID-19 in myriad ways, causing an explosion of research that is broad in scope, varied in methods, and challenging to consolidate. Because policy and practice aimed at helping people live healthier and happier lives requires insight from robust patterns of evidence, this paper provides a rapid and thorough summary of high-quality studies published in 2020 addressing two overarching questions. First, what are the mental health consequences of living through the COVID-19 pandemic? Second, what are the neurological sequelae of contracting COVID-19? Our review of the evidence indicates that some facets of mental health suffered greatly during the early months of the pandemic (e.g., anxiety and depression increased), while other facets (life satisfaction) and correlates (social connection, loneliness) notably displayed resilience. In addition, early neurological data indicate several consequences of contracting COVID-19, both during infection and after recovery. In response to these insights, we present seven recommendations (1 urgent, 2 short-term, 4 ongoing) to support mental health and well-being during the pandemic and beyond.

Complex Network Dynamics in Population Health

2020 ◽  
pp. 45-58
Author(s):  
James Moody ◽  
Dana K. Pasquale
Keyword(s):  
Social Networks ◽  
Network Analysis ◽  
Health Outcomes ◽  
Population Health ◽  
Complex Network ◽  
Well Being ◽  
Complex Relationship ◽  
Future Directions ◽  
And Behavior ◽  
Health And Well Being

People constantly interact with each other and their environment, and these interactions—with whom and with what they interact—are not random. Interactions at multiple levels (cellular, neurological, social, physical, environmental) shape one’s experiences and affect health and well-being. These interactions can be represented as a set of networks that feedback and influence other networks. Here we limit our scope to the complex relationship between human social networks and behavior, which frequently forms a feedback loop, and the effect of this relationship on population health outcomes. This chapter introduces traditional network analysis as it pertains to population health, explores examples of interactions between macro-level networks, and proposes future directions for network analysis

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