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1.
J Health Commun ; 28(sup1): 86-96, 2023 Apr 07.
Article in English | MEDLINE | ID: mdl-37390020

ABSTRACT

National and state data show low adoption of childhood COVID-19 vaccinations, despite emergency use authorizations and availability. We conducted 24 in-depth, semi-structured interviews with Black and Latino parents in New York City (15 in English, 9 in Spanish), who were undecided or somewhat likely to vaccinate their 5 to 11-year-old children in early 2022. The interviews explored the evolution of parental perceptions on childhood COVID-19 vaccines, and were analyzed using a matrix-driven rapid approach to thematic analysis. We present our findings as themes oriented around trust at three levels of the social ecological model. In summary, we found that structural positionality and historical traumas of participants seeded mistrust in institutions and government. This led to parental reliance on personal observations, conversations, and norms within social groups for vaccine decision-making. Our findings also describe key features of trust-building, supportive conversations that shaped the thinking of undecided parents. This study demonstrates how relational trust becomes a key factor in parental vaccine decision-making, and suggests the potential power of community ambassador models of vaccination promotion for increasing success and rebuilding trust with members of the "movable middle."


Subject(s)
COVID-19 Vaccines , COVID-19 , Child , Humans , Child, Preschool , COVID-19 Vaccines/therapeutic use , COVID-19/prevention & control , Vaccination , Hispanic or Latino , Parents
2.
Home Health Care Serv Q ; 42(3): 230-242, 2023.
Article in English | MEDLINE | ID: mdl-36739614

ABSTRACT

Home health aides face a range of stressors that may result in departing the workforce. One stressor that has emerged in multiple qualitative studies as potentially influencing retention is client death. Using 2019 data from a single agency in New York City employing approximately 1700 aides, we used logistic and linear regression to explore case and aide factors associated with workforce outcomes after client death. We found that longer case length (Beta = 0.01, p < .001) was associated with longer return to work for aides experiencing client death and longer job tenure (Beta = -0.002, p = .002) was associated with shorter return to work (n = 67). We found no difference in retention between aides who experienced client death and those who did not (n 216). This analysis suggests the importance of research on the period of time following client death and of offering support to aides after clients die, particularly after longer cases.


Subject(s)
Home Health Aides , Humans , Return to Work , Employment , Qualitative Research , Workforce
3.
Home Health Care Serv Q ; 41(2): 124-138, 2022.
Article in English | MEDLINE | ID: mdl-35212257

ABSTRACT

Home health aides and home care agencies, who operate in a high work stress environment under normal conditions, were placed under extraordinary demands during the COVID-19 pandemic. In this paper, we examine the unfolding effort at one agency in New York City to offer phone-based support calls to aides. We used a qualitative, single case study design involving semi-structured interviews with call staff and agency leaders (n = 9) and analysis of one year of thematic notes from the calls. We found that the calls resulted in multidirectional communication between agency staff and aides, an increased sense of empathy among staff, and a greater integration of aides into the agency's overall infrastructure. We explore how these calls might contribute to aide retention, worker voice, and mental health. We note the facilitators and barriers to implementing this type of job-based support to help other agencies that may be considering similar models.


Subject(s)
COVID-19 , Home Care Agencies , Home Health Aides , Home Health Aides/psychology , Humans , Pandemics/prevention & control , Workplace
4.
Omega (Westport) ; : 302228221078348, 2022 Mar 04.
Article in English | MEDLINE | ID: mdl-35245148

ABSTRACT

Death and dying are woven throughout the work of home care aides, and yet the care they provide at the end of life (EOL) remains poorly understood. This is due in part to the multiple circumstances under which aides provide EOL care. In this paper, we elucidate the EOL care experiences of aides working in home care agencies in New York City. We conducted in-depth interviews with 29 home care aides, and we analyzed these data using inductive, team-based methods. Our findings show that aides may not be aware of or accept a client's EOL status, and they may avoid EOL care. These conditions shape EOL care, and we detail the committed forms of care aides provide when they are aware and accepting. We recommend improved training, support systems, and policy change to enhance aides' contributions to EOL care, while protecting aides' health and well-being.

5.
Qual Health Res ; 31(1): 3-15, 2021 01.
Article in English | MEDLINE | ID: mdl-33074048

ABSTRACT

Few studies integrate work and immigration as intersecting social determinants of health. We synthesize data from 12 focus groups (N = 97) originating from two separate community-engaged studies that originally centered on exploring barriers to health and hazards of work among immigrant Latinx women and men to explore the role of work in their overall health and well-being. The three major interrelated themes we drew from this research-hazards of work, value of work, and building agency to overcome risk-provide insights that can help to reframe and begin to operationalize how community-based health promotion practice might better incorporate workplace issues for Latinx low-wage workers. The value of work, and its subtheme, pride in performing well specifically, could be engaged by workers to actively change conditions for themselves and others. We discuss findings in light of previous occupational health research and implications for community-based intervention design and practice.


Subject(s)
Emigrants and Immigrants , Occupational Health , Emigration and Immigration , Female , Humans , Male , Salaries and Fringe Benefits , Workplace
6.
J Women Aging ; 32(4): 440-461, 2020.
Article in English | MEDLINE | ID: mdl-32475256

ABSTRACT

While there is a growing literature on home care workers, less is known about how home care companies market their services. Through a content analysis of the 19 largest U.S. home care and home health providers' websites, we examined how companies describe services, desired outcomes of care, and job responsibilities and qualifications. Companies actively market family-like relationships as central to "good care". However, companies' emphasis on unmeasurable skills such as compassion and warmth may also create exploitative work environments. Supporting "good care" requires improved data collection, industry oversight, and policy change to recognize socio-emotional care and protect a marginalized workforce.


Subject(s)
Emotions , Home Care Agencies/organization & administration , Home Care Services/organization & administration , Home Health Aides/psychology , Professional-Patient Relations , Aged , Commerce , Empathy , Family/psychology , Female , Home Care Agencies/economics , Humans , Male , Mental Health , Middle Aged , Professionalism , Quality of Life , Trust
7.
Qual Health Res ; 29(3): 382-392, 2019 02.
Article in English | MEDLINE | ID: mdl-30264669

ABSTRACT

While many types of health care workers experience patient death, home care workers do so under vastly different social and economic circumstances. When a client dies, home care workers often lose both a close relationship and a job. Though research suggests that health care workers' grief may frequently be disenfranchised, there is no in-depth study of the mechanisms that disenfranchise home care workers' grief specifically. To address this gap, our study used focus groups and peer interviews between home care workers in New York City. We describe four interrelated grief strategies they employ to navigate social and employer-based "grieving rules." Our findings suggest that home care workers' grief is disenfranchised via employer and societal underestimations of their relationships with clients and their losses when clients die, particularly job loss. Building on our findings, we suggest alterations to agency practices and home care systems to improve support for workers.


Subject(s)
Adaptation, Psychological , Death , Disenfranchised Grief , Health Personnel/psychology , Home Care Services , Adult , Female , Humans , Interviews as Topic , Middle Aged , New York City , Qualitative Research , Social Support , Unemployment/psychology
9.
J Urban Health ; 94(2): 312-314, 2017 04.
Article in English | MEDLINE | ID: mdl-28105584

ABSTRACT

Restaurant workers are less likely to have paid sick leave (PSL) benefits than other professions, despite the fact that they handle food and interact with the public. In this study, we collected and analyzed quantitative and qualitative data on PSL awareness among New York City's restaurant workers and the factors that produced these levels of awareness. We found that 62% of surveyed workers were aware of NYC's law, and that successful outreach requires building broad awareness and ensuring trustworthy sources of information with multiple points of contact. Our research also highlights the importance of immigrant populations in PSL outreach.


Subject(s)
Knowledge , Restaurants/legislation & jurisprudence , Sick Leave/legislation & jurisprudence , Adult , Emigrants and Immigrants , Female , Humans , Male , New York City , Policy
11.
Public Health Nutr ; 19(5): 946-54, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26135913

ABSTRACT

OBJECTIVE: To examine the perspectives and practices of cooks responsible for carrying out healthy meal programmes in publicly funded foodservice, in order to better understand what they consider to be 'good' food and where nutrition and nutritional standards fit into this conceptualization. DESIGN: A qualitative, exploratory study involving in-depth interviews that were conducted with cooks and their supervisors about their work practices and perspectives on providing healthy food for clients. SETTING: Participants were recruited from child-care, after-school, senior-centre and shelter settings that had participated in healthy menu training in New York City, USA. SUBJECTS: Eighteen cooks and nine supervisors working in the aforementioned settings. RESULTS: The views and practices of both cooks and supervisors about what constitutes 'good' food extend beyond a purely nutritional view of goodness to include the importance of addressing hunger and clients' food preferences, among other factors. Cooks address these by interacting with clients and altering recipes and menus in a range of ways to maximize the likelihood of food consumption and enjoyment. These approaches are often, but not always, compatible with setting-specific nutritional guidelines that may be set at the national, state, local or organizational level. CONCLUSIONS: Cooks play a key role in translating nutritional guidelines into what is served. In doing so, they engage in skilled labour and forms of care that increase the ability of public-sector foodservice to address food security and other goals, but these aspects of their work are not widely recognized.


Subject(s)
Cooking , Diet, Healthy , Food Services , Hunger , Institutional Management Teams , Menu Planning , Public Sector , Adolescent , Adult , Aged , Dietary Proteins/administration & dosage , Drinking Water , Evaluation Studies as Topic , Female , Food Preferences , Fruit , Humans , Male , Middle Aged , New York City , Nutrition Policy , Nutritional Status , Nutritive Value , Vegetables , Whole Grains , Young Adult
12.
J Urban Health ; 92(3): 513-26, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25644170

ABSTRACT

The current attention that is being paid to college sexual assault in policy circles and popular media overlooks a critical issue: the possible role played by the urban social environment in intimate partner violence (IPV) risk for the large number of urban commuter college students throughout the USA and beyond. This article helps to illuminate this dynamic using qualitative research collected at an urban commuter campus in New York City. Specifically, we conducted focus groups and in-depth interviews with 18 female undergraduate students, exploring the nature and consequences of IPV in students' lives, perceived prevalence of IPV, and resources for addressing IPV. Our results indicate that college attendance may both elevate and protect against IPV risk for students moving between urban off- and on-campus social environments. Based on this, we present a preliminary model of IPV risk for undergraduate women attending urban commuter colleges. In particular, we find that enrolling in college can sometimes elevate risk of IPV when a partner seeks to limit and control their student partner's experience of college and/or is threatened by what may be achieved by the partner through attending college. These findings suggest a role for urban commuter colleges in helping to mitigate IPV risk through policy formulation and comprehensive ongoing screening and prevention activities.


Subject(s)
Intimate Partner Violence/psychology , Social Environment , Universities , Urban Population , Adolescent , Adult , Educational Status , Female , Focus Groups , Humans , Interviews as Topic , Middle Aged , Risk Factors , Young Adult
13.
Am J Public Health ; 104(1): 11-4, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24228677

ABSTRACT

Meaningful improvements in health require modifying the social determinants of health. As policies are often underlying causes of the living conditions that shape health, policy change becomes a health goal. This focus on policy has led to increasing interest in expanding the focus of community-based participatory research (CBPR) to change not only communities but also policies. To best realize this potential, the relationship between evidence and power in policy change must be more fully explored. Effective action to promote policies that improve population health requires a deeper understanding of the roles of scientific evidence and political power in bringing about policy change; the appropriate scales for policy change, from community to global; and the participatory processes that best acknowledge the interplay between power and evidence.


Subject(s)
Community-Based Participatory Research , Public Health , Public Policy , Evidence-Based Practice , Humans , Social Change
14.
J Appl Gerontol ; 43(9): 1214-1227, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38414156

ABSTRACT

Home care aides play a critical role in the care of older adults, but they do this under difficult working conditions. The COVID-19 pandemic exacerbated aides' stress and worsened their mental health, raising the question of how agencies can better support aides. We explore how home care industry leaders in New York perceived and addressed home care aides' mental health and well-being prior to and during the pandemic through in-depth interviews conducted in 2019 (n = 8 agencies) and 2022 (n = 14 agencies). We found that these topics became more central in leaders' thinking, reflected in a range of new internally and externally funded agency actions, albeit limited by ongoing financial constraints. Maintaining a skilled and reliable aide workforce is critical to societal health but will remain challenging without continued investment in aide support of the kind described in the Surgeon General's Framework for Workplace Mental Health and Well-Being.


Subject(s)
COVID-19 , Home Health Aides , Leadership , Mental Health , Humans , COVID-19/psychology , COVID-19/epidemiology , Home Health Aides/psychology , Male , SARS-CoV-2 , Female , New York , Home Care Services/organization & administration , Adult , Interviews as Topic , Middle Aged , Pandemics
15.
Gerontologist ; 64(7)2024 07 01.
Article in English | MEDLINE | ID: mdl-38794947

ABSTRACT

BACKGROUND AND OBJECTIVES: As long-term care increasingly moves from facilities to the community, paid caregivers (e.g., home health aides, other home care workers) will play an increasingly important role in the care of people with dementia. This study explores the paid caregiver role in home-based dementia care and how that role changes over time. RESEARCH DESIGN AND METHODS: We conducted individual, longitudinal interviews with the paid caregiver, family caregiver, and geriatrician of 9 people with moderate-to-severe dementia in the community; the 29 total participants were interviewed on average 3 times over 6 months, for a total of 75 interviews. Interviews were recorded, transcribed, and analyzed with structured case summaries and framework analysis. RESULTS: Paid caregivers took on distinct roles in the care of each client with dementia. Despite changes in care needs over the study period, roles remained consistent. Paid caregivers, family caregivers, and geriatricians described the central role of families in driving the paid caregiver role. Paid and family caregivers collaborated in the day-to-day care of people with dementia; paid caregivers described their emotional relationships with those they cared for. DISCUSSION AND IMPLICATIONS: Rather than simply providing functional support, paid caregivers provide nuanced care tailored to the needs and preferences of not only each person with dementia (i.e., person-centered care), but also their family caregivers (i.e., family-centered care). Deliberate cultivation of person-centered and family-centered home care may help maximize the positive impact of paid caregivers on people with dementia and their families.


Subject(s)
Caregivers , Dementia , Humans , Caregivers/psychology , Dementia/nursing , Male , Female , Aged , Aged, 80 and over , Longitudinal Studies , Home Care Services/economics , Geriatricians/psychology , Middle Aged , Long-Term Care/economics , Qualitative Research , Home Health Aides/psychology , Family/psychology
16.
JAMA Netw Open ; 7(6): e2415234, 2024 Jun 03.
Article in English | MEDLINE | ID: mdl-38842806

ABSTRACT

Importance: Home health aides and attendants (HHAs) provide essential care to older adults and those with chronic conditions in the home. However, some HHAs struggle with poor mood and stress, which may have been exacerbated by the COVID-19 pandemic. Objective: To elicit HHAs' perspectives toward mental health and well-being, including how their job influences both and how to better support the workforce in the future. Design, Setting, and Participants: For this qualitative study, focus groups and interviews with HHAs were facilitated in English and Spanish from August 17, 2022, to February 9, 2023, in partnership with the 1199SEIU Training and Employment Fund, a benefit fund of the 1199SEIU United Healthcare Workers East and the largest health care union in the US. Included were HHAs at risk for poor mental health and well-being, which were defined as having at least mild or more symptoms on either the 8-item Personal Health Questionnaire depression scale, the 4-item Cohen Perceived Stress Scale, or the University of California, Los Angeles Loneliness Scale. Exposure: Mental health and well-being of HHAs. Main Outcomes and Measures: Focus groups and interviews were audio recorded, professionally transcribed, and translated. A thematic analysis was performed that was informed by Pender's Health Promotion Model and the National Institute for Occupational Safety and Health's Total Worker Health model. Results: A total of 28 HHAs from 14 different agencies participated (mean [SD] age, 54.3 [10.8] years; 26 female [93%]). Seventeen participants (61%) spoke Spanish at home. Five key themes emerged: (1) HHAs' attitudes toward mental health and well-being were influenced by a variety of personal and cultural factors; (2) HHAs' relationships with their patients impacted their mood in both positive and negative ways; (3) structural and organizational aspects of the job, alongside the COVID-19 pandemic, impacted HHAs' mood and stress levels; (4) HHAs used a variety of strategies to cope with their emotions; and (5) HHAs were eager for interventions that can improve their mood, particularly those that bring them closer to their colleagues. Conclusions and Relevance: These findings suggest that HHAs' mental health and well-being may be influenced by both personal and occupational factors. Interventions and policies to better support their emotional well-being on the job are warranted.


Subject(s)
COVID-19 , Focus Groups , Home Health Aides , Mental Health , Qualitative Research , SARS-CoV-2 , Humans , Female , COVID-19/psychology , COVID-19/epidemiology , Male , Adult , Middle Aged , Home Health Aides/psychology , Pandemics , Stress, Psychological/psychology , United States , Depression/psychology
17.
Am J Public Health ; 103(9): e14-20, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23865653

ABSTRACT

The institutional food sector-including food served in schools, child care settings, hospitals, and senior centers-is a largely untapped resource for public health that may help to arrest increasing rates of obesity and diet-related health problems. To make this case, we estimated the reach of a diverse institutional food sector in 1 large municipality, New York City, in 2012, and explored the potential for improving institutional food by building the skills and nutritional knowledge of foodservice workers through training. Drawing on the research literature and preliminary data collected in New York City, we discuss the dynamics of nutritional decision-making in these settings. Finally, we identify opportunities and challenges associated with training the institutional food workforce to enhance nutrition and health.


Subject(s)
Food Services , Nutritional Sciences/education , Decision Making , Diet/methods , Food Services/organization & administration , Government Agencies , Health Promotion/methods , Humans , New York City , Workforce
18.
Sociol Health Illn ; 35(1): 82-96, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22533603

ABSTRACT

The concept of biographical disruption has unique relevance for socioeconomically disadvantaged groups who participate in entry-level job training programmes. In these programmes trainees often suffer from various forms of chronic illness and must arrange these illnesses into a picture of employability. In this article I use ethnographic data and narrative analysis to examine closely two trainees' illness-related experiences, expressions and talk, and find that their ability to present their illnesses in ways that are consistent with programmatic goals is strongly influenced by family support, responsibilities and roles, as well as particular aspects of illness, like the interpretability of symptoms. I also find that the concept of biographical disruption has a curious traction in the world of job training, particularly among job training programme staff who would like to see trainees mobilise a variety of resources to help manage their illness. However, for trainees, many of whom have lived with chronic illness for years, the concept of biographical disruption may be more limited as a tool for understanding the experiences of illness. A more meaningful disruptive force in the lives of trainees appears to be the programme itself and the strategies for dealing with illness that programme staff may extend.


Subject(s)
Chronic Disease , Disabled Persons , Employment , Chronic Disease/psychology , Chronic Disease/rehabilitation , Disabled Persons/education , Disabled Persons/psychology , Disabled Persons/rehabilitation , Employment/psychology , Female , Health Status Disparities , Humans , Job Satisfaction , Male , New England , Rehabilitation, Vocational , Socioeconomic Factors , Surveys and Questionnaires , Young Adult
19.
Article in English | MEDLINE | ID: mdl-36901333

ABSTRACT

Targeted work readiness training is an important approach to help people living with HIV (PLHIV) to overcome their unique barriers to work, while addressing social determinants of health needs. This study assesses the psychosocial impacts of a work readiness training and internship program among HIV peer workers in New York City. From 2014 through 2018, 137 PLHIV completed the training program, and 55 individuals completed both the training and the six-month peer internship. Depression, HIV internalized stigma, self-esteem, HIV medication adherence, patient self-advocacy, and safer sex communication apprehension were used as outcome measures. Paired t-tests were performed to determine if significant score changes occurred at the individual level before and after each training. Our results show that participating in the peer worker training program significantly decreased depression and internalized HIV stigma, and significantly increased self-esteem, medication adherence, and patient self-advocacy. The study underscores that peer worker training programs are important tools to improve not only the work readiness of PLHIV, but also psychosocial and health outcomes. Implications for HIV service providers and stakeholders are discussed.


Subject(s)
HIV Infections , Social Stigma , Humans , Peer Group , Medication Adherence , Self Concept , HIV Infections/psychology
20.
J Appl Gerontol ; 42(4): 747-757, 2023 04.
Article in English | MEDLINE | ID: mdl-36541188

ABSTRACT

Home health aides (HHAs) provide care to many adults with heart failure (HF) in the home. As the demand for HHAs increases, there is a need to promote HHAs' job satisfaction and retention. In this cross-sectional community-partnered study, we examined whether mutuality (e.g., quality of the HHA-patient relationship), is associated with job satisfaction among HHAs caring for adults with HF. Mutuality was assessed with the Mutuality Scale, which measures overall mutuality and its four domains (reciprocity, love and affection, shared pleasurable activities, and shared values). Our final sample of 200 HHAs was primarily female. The mean overall mutuality score was 2.92 out of 4 (SD 0.79). In our final model, overall mutuality and each of the four domains were associated with increased job satisfaction; however, only the shared pleasurable activities domain was significant (aPR: 1.15 [1.03-1.32]). Overall, mutuality may play a role in promoting job satisfaction among HHAs.


Subject(s)
Heart Failure , Home Health Aides , Humans , Female , Job Satisfaction , Cross-Sectional Studies , Heart Failure/therapy
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