Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 159
Filter
Add more filters

Publication year range
1.
Gerontol Geriatr Educ ; 43(3): 315-327, 2022.
Article in English | MEDLINE | ID: mdl-33888037

ABSTRACT

Similar to the nation's majority and racial/ethnic minority populations, Native Hawaiian families provide the bulk of care to loved ones with dementia. Limited research has focused on youth caregivers, who are largely invisible to the eldercare service system. This knowledge gap is especially critical for Native Hawaiians who place a high value on eldercare, often provided in multigenerational homes. To address this gap, we describe the process by which a university-community center developed a culturally responsive storybook on dementia targeted to Native Hawaiian youth. The development process honored community-based participatory research principles grounded in the cultural values and practices of Native Hawaiians, active collaboration of an advisory council, and face-to-face engagement with Native Hawaiian youth. Future directions are shared about culture-based programming and evaluation in dementia care that may be useful in work with other racial/ethnic youth and families.


Subject(s)
Dementia , Geriatrics , Adolescent , Dementia/therapy , Ethnicity , Geriatrics/education , Humans , Minority Groups , Native Hawaiian or Other Pacific Islander
2.
J Gerontol Soc Work ; 65(1): 3-23, 2022 01.
Article in English | MEDLINE | ID: mdl-33974515

ABSTRACT

Native Hawaiian and other Pacific Islander (NHPI) older adults experience various social and health challenges. There is a growing literature linking neighborhood conditions with health, yet few have focused on NHPI older adults. This study examines associations between neighborhood social cohesion and health outcomes (i.e., self-rated health, psychological distress, and memory) in this population. Data from the 2014 Native Hawaiian and Pacific Islander National Health Interview Survey (n=1,045 with respondents aged 50+) were analyzed with logistic regression models. The level of neighborhood social cohesion was determined by responses to items on perceptions of mutual help, dependability, trust, and close relationships within the neighborhood. Higher perceived neighborhood social cohesion was associated with lower odds of having serious psychological distress or memory problems. There was no statistical association of social cohesion with self-rated health. Socially cohesive neighborhoods are important to the health of NHPI. We discuss methods to improve neighborhood social cohesion as a way to promote health equity for NHPI older adults in the United States (U.S.).


Subject(s)
Native Hawaiian or Other Pacific Islander , Social Cohesion , Aged , Hawaii , Health Promotion , Humans , Residence Characteristics , United States
3.
Ethn Health ; 25(7): 982-994, 2020 10.
Article in English | MEDLINE | ID: mdl-29745749

ABSTRACT

Objective: To determine the prevalence and barriers to human papillomavirus (HPV) vaccine uptake among 11-18 year olds in the Hawai'i's four major ethnic groups-Native Hawaiians, Filipinos, Japanese, and Caucasians. Study design: A telephone survey assessed parents' knowledge of HPV and the HPV vaccine, status of their child's HPV vaccine uptake, variables operationalizing the Health Belief Model, and barriers and motivators to uptake. Results: Across the groups, 799 parents completed the survey. About 35% of daughters and 19% of sons had received all three shots. Although ethnic differences in vaccine uptake were seen in bivariate analysis (with significantly lower uptake in Filipino youth), in multivariable logistic regression analysis, only Caucasian parents were significantly less likely to start their sons on the HPV vaccine series compared with Japanese parents (reference group). Having heard about the vaccine, believing in its effectiveness, and older age of the child were also associated with vaccine uptake. Motivators for HPV vaccination were physician's recommendation and wanting to protect one's child. The primary barrier to uptake was lack of knowledge about the vaccine. Conclusions: Findings reinforce the fact that a physician's recommendation and receipt of information about the vaccine are strong motivators for parents to vaccinate their children, regardless of ethnicity.


Subject(s)
Asian/statistics & numerical data , Health Knowledge, Attitudes, Practice , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/therapeutic use , Parents/psychology , White People/statistics & numerical data , Adolescent , Asian/psychology , Child , Cross-Sectional Studies , Female , Hawaii , Humans , Interviews as Topic , Japan/ethnology , Male , Motivation , Papillomavirus Infections/psychology , Patient Acceptance of Health Care , Philippines/ethnology , Physician-Patient Relations , Surveys and Questionnaires , Vaccination/psychology , Vaccination/statistics & numerical data , White People/psychology
4.
Behav Med ; 46(3-4): 258-277, 2020.
Article in English | MEDLINE | ID: mdl-32356679

ABSTRACT

Resilience has conventionally focused on an individual's ability to overcome adversity. Recent research expands on this definition, making resilience a multi-dimensional construct. Native Hawaiians experience health disparities compared to the general population of Hawai'i. Despite the pressing need to address health disparities, minimal research examines resilience factors that serve as buffers for adverse experiences of Native Hawaiians. The purpose of this study was to estimate psychometric properties of scales that measured resilience-based factors through multiple levels using higher-order confirmatory factor analyses (CFA) and ascertain if this construct of resilience mediated or moderated adversity experienced by a sample of Native Hawaiians. Participants included 125 adults who participated in the Hawaiian Homestead Health Survey. Based on higher-order CFA, resilience comprised internal assets measured by hope, satisfaction with life, and environmental mastery, and external resources measured by social support and Native Hawaiian cultural identity. Results of the structural equation models were consistent with literature focusing on resiliency and health. Findings emphasized the importance of enhancing resilience by considering strengths and resources on the individual, interpersonal, and community levels. Findings also demonstrated the need to address adversity factors directly, with a specific need of addressing socio-economic status factors. According to structural equation models, resilience slightly mediated and moderated the effect of adversity related to socio-economic status. These findings have implications for future research exploring resilience as a mediator or moderator of adversity among Native Hawaiians and emphasize a multi-faceted construct of resilience to promote better health outcomes.


Subject(s)
Native Hawaiian or Other Pacific Islander/psychology , Psychometrics/methods , Resilience, Psychological/ethics , Adult , Aged , Female , Hawaii/epidemiology , Health Status Disparities , Health Surveys/methods , Humans , Male , Middle Aged , Models, Theoretical , Reproducibility of Results , Social Support
5.
J Cancer Educ ; 35(1): 210, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31728919

ABSTRACT

The original version of this article unfortunately contained a mistake. The name of "Maile Taualii" is now corrected in the author group of this article.

6.
Fam Community Health ; 42(1): 8-19, 2019.
Article in English | MEDLINE | ID: mdl-30431465

ABSTRACT

Many improvements in health equity are spearheaded by community collaborations working to change policy and social norms. But how can collective efficacy (CE), defined as the willingness and ability of a group to work toward a common good, be increased? Eight articles reporting on interventions aiming to reduce health disparities by improving CE were found for this systematic literature review. All studies showed improvements in CE and most found reduction in disparities, but operationalization of CE varied. Findings support a model of how CE can address health disparities, which can guide standardization of CE interventions and measures.


Subject(s)
Healthcare Disparities/trends , Needs Assessment/trends , Humans , Social Justice
7.
Prev Chronic Dis ; 16: E22, 2019 02 21.
Article in English | MEDLINE | ID: mdl-30789820

ABSTRACT

INTRODUCTION: The prevalence of diabetes varies widely among racial/ethnic groups in Hawai'i. How prevalence varies by age for Asian subgroups and Native Hawaiian/Other Pacific Islanders (NHOPIs) is understudied. We examined diabetes prevalence by age and race/ethnicity and assessed how socioeconomic status and lifestyle behaviors affected prevalence among Japanese, Filipino, Chinese, NHOPI, and white populations in Hawai'i. METHODS: We studied 18,200 subjects aged 18 or older from the Hawai'i Behavioral Risk Factor Surveillance System. We performed Poisson regression analyses to examine the prevalence of diabetes by race/ethnicity, age, sex, marital status, education, income, health care coverage, obesity, smoking and drinking status, physical activity, and fruit and vegetable consumption and examined the interactions of these factors with age and race/ethnicity. RESULTS: We found disparities in diabetes prevalence among respondents aged 35 to 44 and among Asians and NHOPIs, and disparities increased with age. NHOPIs and Filipinos had the highest prevalence of diabetes after controlling for other demographic factors and lifestyle variables. Japanese adults were less likely than NHOPIs and Filipinos to have diabetes; however, whites had the lowest prevalence. Income, physical activity, and obesity were the strongest predictors of diabetes. CONCLUSION: NHOPIs and Filipinos have higher rates of diabetes compared with other races/ethnicities in Hawai'i. More research is needed to reduce diabetes disparities among NHOPI and Filipino populations in Hawai'i. This study also shows the importance of conducting age-specific analyses of racial/ethnic-subgroups for health disparities.


Subject(s)
Asian/statistics & numerical data , Diabetes Mellitus/ethnology , Health Status Disparities , Native Hawaiian or Other Pacific Islander/statistics & numerical data , Adult , Age Distribution , Aged , Aged, 80 and over , Asia/ethnology , Behavioral Risk Factor Surveillance System , Cross-Sectional Studies , Diabetes Mellitus/epidemiology , Female , Hawaii/epidemiology , Hawaii/ethnology , Humans , Male , Middle Aged , Population Surveillance , Prevalence , Risk Factors , Sex Distribution , Young Adult
8.
J Cancer Educ ; 34(3): 446-454, 2019 06.
Article in English | MEDLINE | ID: mdl-29430610

ABSTRACT

The study aims to explore variation in scholarly productivity outcomes by underrepresented status among a diverse sample of researchers in a community-engaged training program. We identified 141 trainees from a web-based survey of researchers in the National Cancer Institute-funded, Community Networks Program Centers (CNPCs) (2011-2016). We conducted a series of multiple logistic regression models to estimate the effect of National Institutes of Health (NIH)-defined underrepresented status on four, self-reported, scholarly productivity outcomes in the previous 5 years: number of publications (first-authored and total) and funded grants (NIH and any agency). Sixty-five percent (n = 92) indicated NIH underrepresented status. In final adjusted models, non-NIH underrepresented (vs. underrepresented) trainees reported an increased odds of having more than the median number of total publications (> 9) (OR = 3.14, 95% CI 1.21-8.65) and any grant funding (OR = 5.10, 95% CI 1.77-14.65). Reporting ≥ 1 mentors (vs. none) was also positively associated (p < 0.05) with these outcomes. The CNPC underrepresented trainees had similar success in first-authored publications and NIH funding as non-underrepresented trainees, but not total publications and grants. Examining trainees' mentoring experiences over time in relation to scholarly productivity outcomes is needed.


Subject(s)
Community Networks/organization & administration , Health Status Disparities , Mentoring/methods , Minority Groups/statistics & numerical data , Neoplasms/ethnology , Research Personnel/education , Training Support/methods , Adult , Biomedical Research/education , Female , Humans , Male , Middle Aged , National Cancer Institute (U.S.) , National Institutes of Health (U.S.) , Research Support as Topic/statistics & numerical data , Surveys and Questionnaires , United States
9.
Prev Chronic Dis ; 15: E59, 2018 05 17.
Article in English | MEDLINE | ID: mdl-29786501

ABSTRACT

INTRODUCTION: Cultural tailoring of interventions can be effective in reducing health disparities by attracting underserved populations to health promotion programs and improving their outcomes. The purpose of this systematic review was to assess what is known about increasing access to and participation in cardiovascular disease (CVD) prevention and control programs among Filipino Americans. METHODS: PubMed MEDLINE, CINAHL, and Sociologic Abstracts were searched for peer-reviewed studies and dissertations conducted in the United States from 2004 through 2016. RESULTS: A total of 347 articles were identified through the search, and 9 articles reporting on 7 interventions focused on CVD prevention in a Filipino American sample were included. All but one intervention used evidence-based curricula, and implementation varied across sites. All but 2 interventions used word-of-mouth advertising from friends, family, and community leaders to increase participation. The Filipino cultural values of food, social relationships, and family were prevalent aspects across interventions tailored for Filipino Americans. Aspects of spirituality and the arts were integrated into only 3 studies. CONCLUSION: Given the burden of CVD in Filipino American populations, tailored interventions rooted in Filipino cultural values are vital to address this known health disparity.


Subject(s)
Asian , Cardiovascular Diseases/prevention & control , Cardiovascular Diseases/therapy , Health Promotion , Peer Influence , Social Support , Cardiovascular Diseases/epidemiology , Humans , United States/epidemiology
10.
J Cross Cult Gerontol ; 32(4): 395-411, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29032489

ABSTRACT

Native Hawaiians, the indigenous people of Hawai'i, were once a healthy and hardy people. But today they are affected by varying social and health disparities that have led to poor social and health outcomes. Most of the research on Hawaiians in general and Native Hawaiian elders in particular has been conducted in Hawai'i, even though the Hawaiian Diaspora has resulted in 45% of this population residing in North America and Alaska. This qualitative study used key informant interviews and focus group methods to examine reasons for migration and perspectives on aging and caregiving in a sample of Native Hawaiian elders and family caregivers residing in Southern California. Findings identified three general themes: discrimination was a factor in their migration from Hawai'i; similarly to non-Hawaiians, they are concerned about challenges associated with aging and caregiving; and Native Hawaiian cultural traditions and values continue to shape their caregiving and service preferences.


Subject(s)
Caregivers , Emigrants and Immigrants , Native Hawaiian or Other Pacific Islander , Aged , California/epidemiology , Caregivers/psychology , Caregivers/statistics & numerical data , Cross-Cultural Comparison , Emigrants and Immigrants/psychology , Emigrants and Immigrants/statistics & numerical data , Emigration and Immigration , Female , Health Status Disparities , Healthcare Disparities , Humans , Male , Middle Aged , Native Hawaiian or Other Pacific Islander/psychology , Native Hawaiian or Other Pacific Islander/statistics & numerical data , Socioeconomic Factors
11.
BMC Health Serv Res ; 16: 300, 2016 07 26.
Article in English | MEDLINE | ID: mdl-27456233

ABSTRACT

BACKGROUND: Potentially preventable hospitalizations (PPH) for heart failure (HF) and diabetes mellitus (DM) cost the United States over $14 billion annually. Studies about PPH typically lack patient perspectives, especially across diverse racial/ethnic groups with known PPH health disparities. METHODS: English-speaking individuals with a HF or DM-related PPH (n = 90) at the largest hospital in Hawai'i completed an in-person interview, including open-ended questions on precipitating factors to their PPH. Using the framework approach, two independent coders identified patient-reported factors and pathways to their PPH. RESULTS: Seventy-two percent of respondents were under 65 years, 30 % were female, 90 % had health insurance, and 66 % had previously been hospitalized for the same problem. Patients' stories identified immediate, precipitating, and underlying reasons for the admission. Underlying background factors were critical to understanding why patients had the acute problems necessitating their hospitalizations. Six, non-exclusive, underlying factors included: extreme social vulnerability (e.g., homeless, poverty, no social support, reported by 54 % of respondents); health system interaction issues (e.g., poor communication with providers, 44 %); limited health-related knowledge (42 %); behavioral health issues (e.g., substance abuse, mental illness, 36 %); denial of illness (27 %); and practical problems (e.g., too busy, 6 %). From these findings, we developed a model to understand an individual's pathways to a PPH through immediate, precipitating, and underlying factors, which could help identify potential intervention foci. We demonstrate the model's utility using five examples. CONCLUSIONS: In a young, predominately insured population, factors well outside the traditional purview of the hospital, or even clinical medicine, critically influenced many PPH. Patient perspectives were vital to understanding this issue. Innovative partnerships and policies should address these issues, including linkages to social services and behavioral health.


Subject(s)
Diabetes Mellitus/therapy , Heart Failure/therapy , Adult , Aged , Asia/ethnology , Critical Pathways , Diabetes Mellitus/ethnology , Female , Hawaii/ethnology , Healthcare Disparities/statistics & numerical data , Heart Failure/ethnology , Humans , Male , Mental Disorders/ethnology , Mental Disorders/therapy , Middle Aged , Native Hawaiian or Other Pacific Islander/ethnology , Qualitative Research , Unnecessary Procedures/statistics & numerical data
12.
Altern Ther Health Med ; 21(5): 64-70, 2015.
Article in English | MEDLINE | ID: mdl-26393993

ABSTRACT

BACKGROUND: Physical inactivity is commonly observed among individuals aged ≥ 60 y. Identified barriers to sedentary older adults beginning activity include low self-efficacy, pre-existing medical conditions, physical limitations, time constraints, and culture. Dancing has the potential to be an attractive physical activity that can be adjusted to fit a target population's age, physical limitations, and culture. OBJECTIVES: This review examined the benefits to physical health of dance interventions among older adults. METHODS: Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, a systematic search using the PubMed database was conducted. Eighteen studies met the inclusion and exclusion criteria and were analyzed for type of intervention, the study's design, participants' demographics, and outcomes, including attrition. RESULTS: The 18 articles reported on studies conducted in North America, South America, Europe, and Asia. Of the styles of dancing, 6 studies used ballroom, 5 used contemporary, 4 used cultural, 1 used pop, and 2 used jazz. Two studies targeted older adults with pre-existing medical conditions. The average age of participants ranged from 52-87 y. Researchers used a variety of measures to assess effectiveness: (1) 3 of 5 (60%) that used measures to assess flexibility showed significant positive results; (2) 23 of 28 (82%) that used measures of muscular strength and endurance showed significant positive changes; (3) 8 of 9 (89%) that used measures of balance showed significant positive changes; (4) 8 of 10 (80%) that used measures of cognitive ability showed significant positive changes; and (5) the one that measured cardiovascular endurance showed significant positive changes. Only 6 studies reported participation, and they found low attrition. CONCLUSIONS: The findings suggest that dance, regardless of its style, can significantly improve muscular strength and endurance, balance, and other aspects of functional fitness in older adults. Future researchers may want to analyze the effects of dance on mental health and explore ways to make this intervention attractive to both genders. Standardizing outcome measures for dance would facilitate meta-analysis.


Subject(s)
Dance Therapy/methods , Dancing/physiology , Motor Skills/physiology , Muscle Strength/physiology , Psychomotor Performance/physiology , Accidental Falls/prevention & control , Aged , Aged, 80 and over , Exercise/physiology , Female , Health Behavior , Humans , Male , Middle Aged , Postural Balance/physiology
13.
J Gen Intern Med ; 29(2): 298-304, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24096723

ABSTRACT

BACKGROUND: Individual health literacy is an established predictor of individual health outcomes. Community-level health literacy may also impact individual health, yet limited research has simultaneously considered the influence of individual and community health literacy on individual health. OBJECTIVE: The study goal was to determine if community health literacy had an independent relationship with individual self-reported health beyond individual health literacy. DESIGN: We used data from the 2008 and 2010 Hawai'i Health Survey, a representative statewide telephone survey. Multilevel models predicted individual self-reported health by both individual and community health literacy, controlling for relevant individual-level (education, race/ethnicity, gender, poverty, insurance status, age, and marital status) and community-level variables (community poverty and community education). PARTICIPANTS: The sample included 11,779 individuals within 37 communities. MAIN MEASURES: Individual health literacy was defined by validated self-reported measurement. Communities were defined by zip code combinations. Community health literacy was defined as the percentage of individuals within a community reporting low health literacy. Census data by ZIP Code Tabulation Areas provided community-level variables. KEY RESULTS: In descriptive results, 18.2 % self-reported low health literacy, and 14.7 % reported self-reported poor health. Community-level low health literacy ranged from 5.37 % to 35.99 %. In final, multilevel models, both individual (OR: 2.00; 95 % CI: 1.63-2.44) and community low health literacy (OR: 1.02; 95 % CI: 1.00-1.03) were significantly positively associated with self-reported poor health status. Each percentage increase of average low health literacy within a community was associated with an approximately 2 % increase in poor self-reported health for individuals in that community. Also associated with poorer health were lower educational attainment, older age, poverty, and non-White race. CONCLUSIONS: Both individual and community health literacy are significant, distinct correlates of individual general health status. Primary care providers and facilities should consider and address health literacy at both community and individual levels.


Subject(s)
Health Literacy/standards , Health Status , Health Surveys/standards , Population Surveillance , Residence Characteristics , Self Report/standards , Adolescent , Adult , Aged , Aged, 80 and over , Female , Hawaii/ethnology , Health Literacy/economics , Health Surveys/economics , Humans , Male , Middle Aged , Population Surveillance/methods , Self Report/economics , Socioeconomic Factors , Young Adult
14.
Ethn Health ; 19(1): 64-85, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24261698

ABSTRACT

OBJECTIVE: Because little is known about promising interventions to prevent and control chronic disease in Korean Americans, we conducted a systematic literature review to investigate: (1) theoretical frameworks and strategies employed by interventions targeting Korean Americans; (2) cultural factors considered by these interventions; and (3) the extent of their success in engaging Korean participants and improving their health. DESIGN: Following the PRISMA guidelines, PubMed, PsycInfo, and Web of Science were searched to identify primary research articles evaluating interventions to prevent or control chronic disease, tailored to Korean Americans, and published from 1980 through 2011. Of 238 articles identified, 21 articles describing16 unique intervention tests met inclusion criteria. These interventions targeted cancer (10), hypertension (2), diabetes (1), mental health (1), tobacco cessation (1), and general health (1). RESULTS: All included studies were published since 2000, reflecting the relatively recent establishment of intervention research with Korean Americans. All 16 programs delivered linguistically appropriate messages and education. The 11 programs that realized significant intervention effects also provided or coordinated social support from culturally relevant and well-trained lay health workers, nurses, or family members during an intervention and/or follow-up period. CONCLUSIONS: Culturally matched and linguistically appropriate messages and education may not be enough to prevent or control chronic disease among immigrant Korean Americans. Culturally sensitive and committed social support should be provided to catalyze behavioral changes and sustain the effect of the interventions.


Subject(s)
Asian/psychology , Chronic Disease/ethnology , Cultural Competency , Health Knowledge, Attitudes, Practice/ethnology , Health Promotion/standards , Adult , Chronic Disease/prevention & control , Chronic Disease/psychology , Databases, Bibliographic , Emigrants and Immigrants/psychology , Health Promotion/methods , Humans , Patient Navigation/methods , Patient Navigation/standards , Republic of Korea/ethnology , Social Support
15.
Prev Sci ; 15(2): 194-204, 2014 Apr.
Article in English | MEDLINE | ID: mdl-23430580

ABSTRACT

Youth violence remains a serious public health issue nationally and internationally. The social ecological model has been recommended as a framework to design youth violence prevention initiatives, requiring interventions at the micro-, meso-, exo-, and macro-levels. However, documentation of interventions at the macro-level, particularly those that address policy issues, is limited. This study examines a recommendation in the literature that formalized collaborations play a vital role in stimulating macro-level policy change. The purpose of this systematic literature review is to examine existing youth violence prevention collaborations and evaluate their policy-related outcomes. The search found 23 unique collaborations focused on youth violence prevention. These were organized into three groups based on the "catalyst" for action for the collaboration-internal (momentum began within the community), external (sparked by an external agency), or policy (mandated by law). Findings suggest that internally catalyzed collaborations were most successful at changing laws to address youth violence, while both internally and externally catalyzed collaborations successfully attained policy change at the organizational level. A conceptual model is proposed, describing a potential pathway for achieving macro-level change via collaboration. Recommendations for future research and practice are suggested, including expansion of this study to capture additional collaborations, investigation of macro-level changes with a primary prevention focus, and improvement of evaluation, dissemination, and translation of macro-level initiatives.


Subject(s)
Community Networks/organization & administration , Cooperative Behavior , Juvenile Delinquency/prevention & control , Primary Prevention/organization & administration , Violence/prevention & control , Adolescent , Community Health Services/organization & administration , Female , Humans , Male , Social Change , Social Work/organization & administration
16.
J Cancer Educ ; 29(3): 570-6, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24683042

ABSTRACT

Genomic science represents a new frontier for health research and will provide important tools for personalizing health care. Biospecimen-based research is an important mechanism for expanding the genomic research capacity, and indigenous peoples are a target of biospecimen-based research due to their relative isolation and the potential to discover rare or unique genotypes. This study explored Native Hawaiian perceptions of and expectations for biobanking. Ten discussion groups were conducted with Native Hawaiians (N = 92), who first heard a presentation on biobanking. Six themes emerged: (1) biobank governance by the Native Hawaiian community, (2) research transparency, (3) priority of Native Hawaiian health concerns, (4) leadership by Native Hawaiian scientists accountable to community, (5) re-consenting each time specimen is used, and (6) education of Native Hawaiian communities. Considered together, these findings suggest that biobanking should be guided by six principles that comprise "G.R.E.A.T. Research" (Governance, Re-consent, Education, Accountability, Transparency, Research priorities). These recommendations are being shared with biobanking facilities in Hawai'i as they develop protocols for biobanking participation, governance, and education. These findings also inform researchers and indigenous peoples throughout the world who are working on biobanking and genomic research initiatives in their nations.


Subject(s)
Biological Specimen Banks , Biomedical Research , Community Networks/organization & administration , Ethnicity/psychology , Health Knowledge, Attitudes, Practice , Native Hawaiian or Other Pacific Islander/psychology , Neoplasms/prevention & control , Neoplasms/psychology , Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult
17.
J Cross Cult Gerontol ; 29(2): 131-51, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24659060

ABSTRACT

Native Hawaiians, the indigenous people of Hawai'i, are affected by varying social and health disparities that result in high prevalence of chronic disease, early onset of disability, and shorter life expectancy compared to other ethnic groups in Hawai'i. Six listening meetings were conducted, involving 41 community-dwelling kupuna (Native Hawaiian elders) and 'ohana (family) caregivers to investigate health and care preferences that offer the potential for improving well-being in later life for Native Hawaiian elders. As background, we provide three explanatory perspectives and theories­life course perspective, minority stress theory, and historical trauma­that guided the design of this study and provided the study's context. A number of overarching themes and subthemes were identified, some of which point to universal concerns with age and caregiving (such as challenges and costs associated with growing old and caregiving) and others that are culturally specific (such as influence of culture and social stressors, including discrimination, on health needs and care preferences). Results give further support to the urgency of affordable, accessible, and acceptable programs and policies that can respond to the growing health and care needs of native elders and family caregivers.


Subject(s)
Adaptation, Psychological , Attitude to Health/ethnology , Caregivers/psychology , Cultural Characteristics , Health Status , Home Nursing/methods , Aged, 80 and over , Female , Hawaii , Health Services Needs and Demand , Humans , Male , Self Concept , Social Perception
18.
Front Public Health ; 12: 1427605, 2024.
Article in English | MEDLINE | ID: mdl-39091527

ABSTRACT

Loneliness in older persons is a major risk factor for adverse health outcomes. Before the COVID-19 pandemic led to unprecedented isolation and hampered programs aimed at preventing or reducing loneliness, many interventions were developed and evaluated. However, previous reviews provide limited or conflicting summaries of intervention effectiveness. This systematic review aimed to assess previous review quality and bias, as well as to summarize key findings into an overarching narrative on intervention efficacy. The authors searched nine electronic databases and indices to identify systematic reviews of interventions to reduce loneliness in older people prior to the COVID-19 pandemic; 6,925 records were found initially. Of these, 19 reviews met inclusion criteria; these encompassed 101 unique primary intervention studies that varied in research design, sample size, intervention setting, and measures of loneliness across 21 nations. While 42% of reviews had minimal risk of bias, only 8% of primary studies appraised similarly. Among the 101 unique articles reviewed, 63% of tested interventions were deemed by article author(s) as effective or partially effective. Generally, interventions that included animals, psychological therapies, and skill-building activities were more successful than interventions focused on social facilitation or health promotion. However, interventions that targeted multiple objectives aimed at reducing loneliness (e.g., improving social skills, enhancing social support, increasing social opportunities, and changing maladaptive social cognition) were more effective than single-objective interventions. Future programs should incorporate multiple approaches, and these interventions should be rigorously tested.


Subject(s)
COVID-19 , Loneliness , Humans , Loneliness/psychology , Aged , COVID-19/psychology
19.
AIDS Care ; 25(4): 515-23, 2013.
Article in English | MEDLINE | ID: mdl-23005581

ABSTRACT

With the increasing prevalence of premarital sex among college students in China, our aim was to examine prevalence and determinants of condom use among sexually active female undergraduates at 16 university campuses in Wuhan. Questionnaires were distributed to 5076 unmarried female undergraduates, recruited using randomized cluster sampling by type of university and student major and grade, and anonymously completed questionnaires were received from 4769 (94% of enrollees). The complex samples logistic regression was used to examine factors associated with condom use, yielding odds ratios and 95% confidence intervals. Of 4769 female students, 863 (18.1%) reported ever having sexual intercourse. Of these, 19.8% used a condom in their first sexual encounter, and these students were more likely to age 20 or older at first intercourse, and less likely to live in countryside during middle school period, and majoring in the arts. Fully 30% of those having intercourse reported never or seldom or sometimes using condoms in the past 12 months. Students using condoms consistently in the past 12 months were more likely majoring in science and technology, to believe that condoms are the safest way to prevent STD and unwanted pregnancy, and to have used a condom at first intercourse; they were less likely to live in countryside during middle school period, and to report multiple sexual partners since initiating sexual behavior. These results suggested that a larger subset of Chinese female undergraduates is engaged in unprotected, premarital sex, and interventions provided for them should stress the importance of delaying sexual initiation, using condoms from the very first sexual encounter, and consistently using condoms after initiating sex.


Subject(s)
Condoms/statistics & numerical data , Sexual Behavior/statistics & numerical data , Sexually Transmitted Diseases/epidemiology , Students/statistics & numerical data , Adolescent , Adult , China , Female , Health Knowledge, Attitudes, Practice , Humans , Prevalence , Sex Education , Sexual Behavior/psychology , Sexual Partners/psychology , Sexually Transmitted Diseases/prevention & control , Sexually Transmitted Diseases/psychology , Students/psychology , Surveys and Questionnaires , Universities
20.
J Health Commun ; 18 Suppl 1: 242-55, 2013.
Article in English | MEDLINE | ID: mdl-24093359

ABSTRACT

The authors examined the relationship between low health literacy (LHL), limited English proficiency (LEP), and meeting current U.S. Preventive Service Task Force colorectal cancer (CRC) screening guidelines for Asians and Whites in California. For 1,478 Asian and 14,410 White respondents 50-75 years of age in the 2007 California Health Interview Survey, the authors examined meeting CRC screening guidelines using multivariable logistic models by LEP and LHL separately and in combination. Analyses were run with the full sample, then separately for Whites and Asians controlling for demographics and insurance. For those with LEP, patient-provider language concordance and CRC screening was examined. Overall, respondents with LEP and LHL were the least likely to meet CRC screening guidelines (36%) followed by LEP-only (45%), LHL-only (51%), and those with neither LHL nor LEP (59%), a hierarchy that remained significant in multivariable models. For Whites, LHL-only was associated with screening, whereas LEP-only and LEP and LHL were significant for Asians. Having a language concordant provider was not significantly associated with CRC screening among those with LEP. Health literacy is associated with CRC screening, but English proficiency is also critical to consider. Asians with both LEP and LHL appear particularly vulnerable to cancer screening disparities.


Subject(s)
Asian/statistics & numerical data , Colorectal Neoplasms/ethnology , Communication Barriers , Early Detection of Cancer/statistics & numerical data , Health Literacy/statistics & numerical data , Language , White People/statistics & numerical data , Aged , California , Colorectal Neoplasms/prevention & control , Educational Status , Female , Health Care Surveys , Healthcare Disparities , Humans , Male , Middle Aged , Multivariate Analysis , Practice Guidelines as Topic
SELECTION OF CITATIONS
SEARCH DETAIL