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1.
J Immigr Minor Health ; 23(4): 725-732, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33034793

ABSTRACT

Sickle cell disease (SCD) is a genetic disorder predominantly affecting people of African descent and is associated with significant morbidity and mortality. To improve SCD outcomes, the National Heart Lung and Blood Institute funded eight centers to participate in the SCD Implementation Consortium. Sites were required to each recruit 300 individuals with SCD, over 20 months. We aim to describe recruitment strategies and challenges encountered. Participants aged 15-45 years with confirmed diagnosis of SCD were eligible. Descriptive statistics were used to analyze the effectiveness of each recruitment strategy. A total of 2432 participants were recruited. Majority (95.3%) were African American. Successful strategies were recruitment from clinics (68.1%) and affiliated sites (15.6%). Recruitment at community events, emergency departments and pain centers had the lowest yield. Challenges included saturation of strategies and time constraints. Effective recruitment of participants in multi-site studies requires multiple strategies to achieve adequate sample sizes.


Subject(s)
Anemia, Sickle Cell , Black or African American , Emergency Service, Hospital , Humans , Registries
2.
Soc Sci Med ; 232: 289-297, 2019 07.
Article in English | MEDLINE | ID: mdl-31121439

ABSTRACT

Cervical cancer is a preventable disease. HPV infection has been linked to more than 90% of cervical cancers. A vaccine to prevent the acquisition of HPV has been available since 2006. The purpose of this study was to investigate women's perceptions of cervical cancer prevention, including HPV vaccination. A reproductive justice framework guided data collection and analysis. In 2016, researchers conducted 70 in-depth, semi-structured qualitative interviews with women aged 19-78 years in South Carolina. A purposive sampling approach was employed to maximize requisite variety based on social, economic, and environmental axes of inequality. Participants self-identified as white (53%), African American (33%), and Hispanic (9%). Data analysis included an inductive constant comparative method to identify patterns and themes across the interviews. Misinformation about the prevalence and risk of HPV and cervical cancer led to "othering" of women with HPV-related diagnoses based on the flawed assumption of not being at risk. Participants described a lack of knowledge about the effectiveness and safety of the HPV vaccine. Social norms influenced participants' perceptions of HPV vaccination and cervical cancer, including concerns about sexual activity and intergenerational communication. Participants' social construction of identity, including race/ethnicity, socioeconomic position, ability, age, gender, sexual orientation, and immigration status, impacted their perceptions of cervical cancer screening and the HPV vaccine. In particular, participants believed that the HPV vaccine was "only for girls" and identified gender norms that limited uptake. Participants described barriers to accessing health care and cervical cancer screening, including cost, health insurance, and life changes (e.g., pregnancy, relocating). Many participants experienced an abnormal Papanicolaou test and described follow-up care, including biopsies and treatment for cervical dysplasia. Findings from this study offer insight into women's identity and perceptions of cervical cancer prevention. Results provide practical recommendations to increase women's agency in the development of successful public health interventions.


Subject(s)
Papillomavirus Infections/complications , Reproductive Health Services/standards , Social Justice , Uterine Cervical Neoplasms/prevention & control , Adult , Aged , Early Detection of Cancer/methods , Early Detection of Cancer/psychology , Early Detection of Cancer/standards , Female , Focus Groups/methods , Health Knowledge, Attitudes, Practice , Humans , Mass Screening/methods , Mass Screening/psychology , Mass Screening/standards , Middle Aged , Papillomavirus Infections/psychology , Qualitative Research , Reproductive Health Services/trends , South Carolina , Uterine Cervical Neoplasms/diagnosis
3.
J Cancer Educ ; 34(3): 412-422, 2019 06.
Article in English | MEDLINE | ID: mdl-29330754

ABSTRACT

In the United States (U.S.), Hispanics experience breast cancer disparities. Breast cancer is the leading cause of cancer-related death among Hispanic women, and Hispanic women receive mammography screening at lower rates than some other ethnic groups. This low rate of screening mammography is associated with increased risk for possible late-stage diagnosis and lower survival rates. Educational interventions could play a role in increasing screening mammography rates among Hispanic women. This systematic review synthesized the current literature on educational interventions to increase mammography screening among Hispanic women. The review included studies published between May 2003 and September 2017 with experimental and quasi-experimental interventions to increase mammography screening among Hispanics in the U.S. Five studies out of an initial 269 studies met inclusion criteria for the review. All studies employed an interpersonal intervention strategy with community health workers, or promotoras, to deliver the mammography screening intervention. For each study, odds ratios (OR) were calculated to estimate intervention effectiveness based on similar follow-up time periods. The study ORs resulted in a narrow range between 1.02 and 2.18, indicating a low to moderate intervention effect for these types of interpersonal cancer education interventions. The summary OR for the random effects model was 1.67 (CI 1.24-2.26). Hispanics exhibit lower levels of adherence to screening mammography than non-Hispanic whites. Interpersonal cancer education interventions such as the use of promotoras may help to mediate the impact of barriers to receiving a mammogram such as low health literacy, deficits in knowledge about the benefits of screening, and low awareness of the availability of screening services.


Subject(s)
Breast Neoplasms/prevention & control , Community Health Workers/education , Early Detection of Cancer/statistics & numerical data , Health Education , Hispanic or Latino/education , Mammography/statistics & numerical data , Patient Acceptance of Health Care/ethnology , Breast Neoplasms/ethnology , Breast Neoplasms/psychology , Early Detection of Cancer/psychology , Female , Humans , Mammography/psychology , United States
4.
J Agromedicine ; 24(1): 15-25, 2019 01.
Article in English | MEDLINE | ID: mdl-30317928

ABSTRACT

Heat-related illness (HRI) among migrant and seasonal farmworkers is an occupational risk addressed through varying mitigation strategies by individual workers and supervisors. The purpose of this pilot study was to describe farmworkers' experience with HRI prevention strategies and assess HRI information seeking preferences, especially the feasibility of using mobile phone apps to access this information. Five focus groups were administered to Hispanic farmworkers in South Carolina. Questions included the following topics: health information seeking preferences; farmworkers' perceptions of occupational risks; coping strategies; past experiences with HRIs; water, rest, and shade practices; access to health care; and any employer-provided training received. There was consensus across the groups that the workers at highest risk for HRIs were either inexperienced or new workers in the fields. Farmworkers ascribed responsibility for one's well-being while working in the heat more as an individual factor than as an employer's responsibility. Farmworkers received training on the OSHA Heat Safety Tool app and provided positive feedback about the educational content and temperature information warnings. These findings suggest the potential for supervisors to take a more active role in heat safety education using mobile technology.


Subject(s)
Farmers , Heat Stress Disorders/prevention & control , Hispanic or Latino , Mobile Applications , Focus Groups , Health Services Accessibility , Humans , Occupational Exposure/prevention & control , Occupational Health , Pilot Projects , South Carolina , Transients and Migrants
5.
BMC Health Serv Res ; 18(1): 310, 2018 05 02.
Article in English | MEDLINE | ID: mdl-29716586

ABSTRACT

BACKGROUND: South Carolina is considered a "new destination" state for Latino immigrants. Language barriers, transportation difficulties, low socioeconomic status, inflexible work schedules, different cultural norms, and anxiety and fear related to the current anti-immigrant political climate all negatively impact Latino immigrants' frequency of contact with the health care system, and consequently they suffer poor health outcomes. The study objective was to explore uninsured Latina immigrant women's access to health care and alternative treatment strategies in coastal South Carolina. METHODS: The study design was a qualitative interview design. Thirty women participated in semi-structured interviews in community sites. Thematic analysis identified salient categories of topics across interview participants. RESULTS: The themes were organized into four primary categories including: 1) Barriers and Facilitators to Healthcare, 2) Health Behaviors and Coping Mechanisms, 3) Disease Management Strategies, and 4) Cultural Factors. Participants demonstrated determination for accessing care but reported that their primary health care access barriers included the high cost of services, lack of health insurance, family and work responsibilities, and language barriers. Coping mechanisms included activating their social networks, visiting family and friends and assisting one another with navigating life challenges. CONCLUSION: Participants overcame obstacles to obtain healthcare for themselves and their family members despite the multiple barriers presented. Social networks were leveraged to protect against some of the negative effects of financial barriers to health care access.


Subject(s)
Emigrants and Immigrants/statistics & numerical data , Health Care Costs , Health Services Accessibility/statistics & numerical data , Hispanic or Latino/statistics & numerical data , Medically Uninsured , Adaptation, Psychological , Adult , Communication Barriers , Female , Health Services Accessibility/economics , Humans , Middle Aged , South Carolina , Young Adult
6.
J Racial Ethn Health Disparities ; 5(3): 588-597, 2018 06.
Article in English | MEDLINE | ID: mdl-28702925

ABSTRACT

OBJECTIVES: This study aims to examine prevalence and correlates of cervical cancer screening utilization and adherence among a growing population of Hispanic immigrant women in coastal South Carolina. METHODS: We conducted a cross-sectional survey of 196 women to assess recency of screening and hypothesized study predictors (health status, beliefs, self-efficacy, having a regular provider, barriers to screening, and trust in providers). Multiple ordinal logistic regressions identified final covariates which would predict recency of screening. RESULTS: Approximately 84% of women were up-to-date with their Pap tests and 47% had received a Pap test in the previous year. In the adjusted analyses, having a regular provider and having a chronic medical condition were significantly associated with recency of Pap test. CONCLUSIONS: Differences in cervical cancer screening for participants were partially explained by psychosocial factors, health status, and individual and structural barriers to healthcare.


Subject(s)
Early Detection of Cancer/statistics & numerical data , Emigrants and Immigrants/statistics & numerical data , Hispanic or Latino/statistics & numerical data , Uterine Cervical Neoplasms/diagnosis , Adult , Chronic Disease/epidemiology , Cross-Sectional Studies , Female , Health Behavior , Health Status , Humans , Logistic Models , Middle Aged , Papanicolaou Test , Self Efficacy , South Carolina , Trust , Vaginal Smears , Young Adult
7.
Hisp Health Care Int ; 15(3): 113-120, 2017 09.
Article in English | MEDLINE | ID: mdl-29164938

ABSTRACT

INTRODUCTION: The study hypothesized that sociocultural factors would be associated with breast cancer screening within the past 2 years among Latina immigrant women. METHOD: This study employed a survey design and included 82 Latina immigrant female participants 40 to 64 years of age for the analysis. Two multivariable binary logistic regression models were estimated, one for the sociocultural deterrents and the other for the symptomatic deterrents from the Cultural Cancer Screening Scale. RESULTS: The results indicated two constructs of the Cultural Cancer Screening Scale, sociocultural deterrents (odds ratio = 2.00; 95% confidence interval = 1.04-3.86) and symptomatic deterrents (odds ratio = 1.65; 95% confidence interval = 1.08-2.54), were associated with screening in the past 2 years, when adjusting for sociodemographic and health-related characteristics. CONCLUSION: These findings provide evidence for the importance of sociocultural factors in Latina immigrant women's timely mammography screening.


Subject(s)
Breast Neoplasms , Cultural Characteristics , Emigrants and Immigrants , Hispanic or Latino , Mammography , Mass Screening , Patient Acceptance of Health Care/ethnology , Adult , Breast Neoplasms/diagnosis , Breast Neoplasms/ethnology , Humans , Logistic Models , Middle Aged , Odds Ratio , Surveys and Questionnaires
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