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2012-2018 Health Atlas for Asian Americans, Native Hawaiians, and Pacific Islanders A comprehensive look at AA and NH&PI health in the U.S.

Wyatt, LC; Russo, R; Kranick, J; Elfassy, T; Kwon, SC; Wong, JA; Ðoàn, LN; Trinh-Shevrin, C; Yi, SS
New York : NYU Center for the Study of Asian American Health, 2021
Extent: 76 p.
ISBN: n/a
CID: 5295542

Asian American, Native Hawaiian, and Pacific Islander Maps Book 2010-2017 : Exploring Geographic And Migratory Patterns Among Asian American, Native Hawaiian, And Pacific Islander

Spoer, B; Hsieh, P; Juul, F; Lampe, T; Chen, A; Wong, JA; Ðoàn, LN; Kwon, Simona C; Trinh-Shevrin, C; Thorpe, L; Yi, Stella S
New York : NYU Center for the Study of Asian American Health, 2021
ISBN: n/a
CID: 5295552

Social Media Use and Misinformation Among Asian Americans During COVID-19

Chong, Stella K; Ali, Shahmir H; Ðoàn, Lan N; Yi, Stella S; Trinh-Shevrin, Chau; Kwon, Simona C
Social media has been crucial for seeking and communicating COVID-19 information. However, social media has also promulgated misinformation, which is particularly concerning among Asian Americans who may rely on in-language information and utilize social media platforms to connect to Asia-based networks. There is limited literature examining social media use for COVID-19 information and the subsequent impact of misinformation on health behaviors among Asian Americans. This perspective reviews recent research, news, and gray literature to examine the dissemination of COVID-19 misinformation on social media platforms to Chinese, Korean, Vietnamese, and South Asian Americans. We discuss the linkage of COVID-19 misinformation to health behaviors, with emphasis on COVID-19 vaccine misinformation and vaccine decision-making in Asian American communities. We then discuss community- and research-driven responses to investigate misinformation during the pandemic. Lastly, we propose recommendations to mitigate misinformation and address the COVID-19 infodemic among Asian Americans.
PMCID:8795661
PMID: 35096736
ISSN: 2296-2565
CID: 5361932

Influence of organizational and social contexts on the implementation of culturally adapted hypertension control programs in Asian American-serving grocery stores, restaurants, and faith-based community sites: a qualitative study

Gore, Radhika; Patel, Shilpa; Choy, Catherine; Taher, Md; Garcia-Dia, Mary Joy; Singh, Hardayal; Kim, Sara; Mohaimin, Sadia; Dhar, Ritu; Naeem, Areeg; Kwon, Simona C; Islam, Nadia
Hypertension affects a third of U.S. adults and is especially high among Asian American groups. The Racial and Ethnic Approaches to Community Health for Asian AmeRicans (REACH FAR) project delivers culturally adapted, evidence-based hypertension-related programs to Bangladeshi, Filipino, Korean, and Asian Indian communities in New York and New Jersey through 26 sites: ethnic grocery stores, restaurants, and Muslim, Christian, and Sikh faith-based organizations. Knowledge of the implementation mechanisms of culturally adapted programs is limited and is critical to inform the design and execution of such programs by and in community sites. We applied four categories of the Consolidated Framework for Implementation Research-intervention and individuals' characteristics, inner and outer setting-to analyze factors influencing implementation outcomes, that is, site leaders' perceptions about adopting, adapting, and sustaining REACH FAR. We conducted semistructured interviews with 15 leaders, coded them for implementation outcomes, and recoded them to identify contextual factors. Our findings show that REACH FAR resonated in sites where leaders perceived unhealthy diet and lifestyles in their communities (intervention characteristics), sites had historically engaged in health programs as a public-service mission (inner setting), and leaders identified with this mission (individuals' characteristics). Site leaders strived to adapt programs to respond to community preferences (outer setting) without compromising core objectives (inner setting). Leaders noted that program sustainability could be impeded by staff and volunteer turnover (inner setting) but enhanced by reinforcing programs through community networks (outer setting). The findings suggest that to facilitate implementation of culturally adapted health behavior programs through community sites, interventions should reinforce sites' organizational commitments and social ties.
PMID: 31260065
ISSN: 1613-9860
CID: 3967852

Neighborhood social cohesion and disease prevention in Asian immigrant populations

Ali, Shahmir H; Yi, Stella S; Wyatt, Laura C; Misra, Supriya; Kwon, Simona C; Trinh-Shevrin, Chau; Islam, Nadia S
In the United States (US), chronic disease risk factors are highly prevalent among Asian immigrant communities, who also exhibit low health screening rates. Perceived neighborhood social cohesion (NSC) has been associated with preventive healthcare use in the general US population, although it remains unexplored among Asian Americans (AAs). The aim of this study is to evaluate the association between NSC and preventive screening for hypertension, high cholesterol, diabetes, and depression among East, South and Southeast Asian American (EAA, SAA, SEAA) communities in New York City (NYC) using cross-sectional, locally collected data from 2013 to 2016. NSC was assessed using a 4-question scale to create an additive score between 4 and 16 and was analyzed both as a continuous and categorial variable (High, Medium, and Low tertiles). Recent screening was defined as a check-up within the last year for each of the included health conditions. A one-unit increase in NSC score was associated with increased odds of recent screening for high cholesterol in EAAs (AOR = 1.09, 95%CI:1.00-1.20); for high cholesterol, diabetes, and depression in SAAs (AOR = 1.08, 95%CI:1.00-1.20; AOR = 1.07, 95%CI:1.00-1.15; AOR = 1.15, 95%CI:1.06-1.25); and with high cholesterol among SEAAs (AOR = 1.12, 95%CI:1.00-1.25). Overall, NSC was an important facilitator for preventive screening behaviors for specific conditions in different groups, though was consistently associated with screening for high cholesterol in our sample. Enhancing NSC through family and community-based programming may be one strategy to encourage screening for preventive behaviors, though more research is needed to elucidate a precise mechanism.
PMCID:7581417
PMID: 33148519
ISSN: 1096-0260
CID: 4716252

Disparities in Sources of Added Sugars and High Glycemic Index Foods in Diets of US Children, 2011-2016

Russo, Rienna G; Peters, Brandilyn A; Salcedo, Vanessa; Wang, Vivian Hc; Kwon, Simona C; Wu, Bei; Yi, Stella
INTRODUCTION/BACKGROUND:Added sugars and high glycemic index (GI) foods might play a role in cardiometabolic pathogenesis. Our study aimed to describe the top sources of added sugars and types of high GI foods in diets of children by race/ethnicity. METHODS:We examined data for 3,112 children, aged 6 to 11 years from the National Health and Nutrition Examination Survey (NHANES), 2011 to 2016. Mean intake was estimated and linear regression models tested for differences by race/ethnicity. Population proportions for food sources were created and ranked, accounting for survey weighting when appropriate. RESULTS:Asian American and Mexican American children had the lowest reported added sugar intake. Cereals were observed to contribute highly to added sugar intake. Soft drinks did not contribute as much added sugar intake for Asian American children as it did for children of other races/ethnicities. Asian American children consumed significantly more high GI foods than other groups. Types of high GI foods differed meaningfully across racial/ethnic groups (ie, Mexican American: burritos/tacos; other Hispanic, White, and Black: pizza; Asian American: rice). Rice accounted for 37% of total high GI foods consumed by Asian American children. CONCLUSIONS:Sources of added sugars and types of high GI foods in children's diets vary across racial/ethnic groups. Targeting foods identified as top sources of added sugars for all race/ethnicities and focusing on substitution of whole grains may reduce obesity, diabetes, and related cardiometabolic risk more equitably.
PMCID:7665514
PMID: 33155971
ISSN: 1545-1151
CID: 4684172

Alzheimer's Disease Screening Tools for Asian Americans: A Scoping Review

Lim, Sahnah; Chong, Stella; Min, Deborah; Mohaimin, Sadia; Roberts, Timothy; Trinh-Shevrin, Chau; Kwon, Simona C
With growing numbers of aging Asian Americans, Native Hawaiians, and Pacific Islanders (AANHPIs), the availability of culturally and linguistically appropriate screening tools for Alzheimer's disease and its related dementias (ADRD) is needed. The aim of this scoping review is to summarize the tools that have been adapted for and validated among the AANHPI population. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) protocol for systematic reviews, six databases were searched for peer-reviewed articles describing ADRD among AANHPIs. Among 1,477 articles screened for inclusion, 15 articles were included in the final analysis. Results showed a paucity of studies that psychometrically validate tools among this population. Furthermore, studies that culturally adapted and/or translated existing tools mostly targeted East Asian American populations. Our review provides a first step in mapping the extant literature on ADRD screening tools for this underresearched population and will serve as a guide for future research, policy, and intervention.
PMID: 33100109
ISSN: 1552-4523
CID: 4647152

Profiling Clinical Research Activity at an Academic Medical Center by Using Institutional Databases: Content Analysis

Langford, Aisha; Sherman, Scott; Thornton, Rachel; Nightingale, Kira; Kwon, Simona; Chavis-Keeling, Deborah; Link, Nathan; Cronstein, Bruce; Hochman, Judith; Trachtman, Howard
BACKGROUND:It is important to monitor the scope of clinical research of all types, to involve participants of all ages and subgroups in studies that are appropriate to their condition, and to ensure equal access and broad validity of the findings. OBJECTIVE:We conducted a review of clinical research performed at New York University with the following objectives: (1) to determine the utility of institutional administrative data to characterize clinical research activity; (2) to assess the inclusion of special populations; and (3) to determine if the type, initiation, and completion of the study differed by age. METHODS:Data for all studies that were institutional review board-approved between January 1, 2014, and November 2, 2016, were obtained from the research navigator system, which was launched in November 2013. One module provided details about the study protocol, and another module provided the characteristics of individual participants. Research studies were classified as observational or interventional. Descriptive statistics were used to assess the characteristics of clinical studies across the lifespan, by type, and over time. RESULTS:A total of 22%-24% of studies included children (minimum age <18 years) and 4%-5% focused exclusively on pediatrics. Similarly, 64%-72% of studies included older patients (maximum age >65 years) but only 5%-12% focused exclusively on geriatrics. Approximately 85% of the studies included both male and female participants. Of the remaining studies, those open only to girls or women were approximately 3 times as common as those confined to boys or men. A total of 56%-58% of projects focused on nonvulnerable patients. Among the special populations studied, children (12%-15%) were the most common. Noninterventional trial types included research on human data sets (24%), observational research (22%), survey research (16%), and biospecimen research (8%). The percentage of projects designed to test an intervention in a vulnerable population increased from 17% in 2014 to 21% in 2015. CONCLUSIONS:Pediatric participants were the special population that was most often studied based on the number of registered projects that included children and adolescents. However, they were much less likely to be successfully enrolled in research studies compared with adults older than 65 years. Only 20% of the studies were interventional, and 20%-35% of participants in this category were from vulnerable populations. More studies are exclusively devoted to women's health issues compared with men's health issues.
PMID: 32831180
ISSN: 2369-2960
CID: 4575082

Gender Differences in Acculturative Stress and Habitual Sleep Duration in Korean American Immigrants

Park, Chorong; Spruill, Tanya M; Butler, Mark J; Kwon, Simona C; Redeker, Nancy S; Gharzeddine, Rida; Whittemore, Robin
Korean American immigrants (KAIs) face diverse sociocultural stressors in the acculturation process. While stress is known to cause short sleep, little is known about how acculturative stress affects sleep differently for KAI men and women. The purpose of this cross-sectional study was to examine gender differences in the association between diverse domains of acculturative stress and sleep duration among KAIs. Middle-aged KAIs were recruited in community settings and online. KAIs completed validated measures of acculturative stress (homesickness, social isolation, employment barriers, discrimination, civic disengagement, and family problems) and sleep duration. Multiple linear regression analysis was performed and stratified by gender. 343 KAIs participated (mean age = 41 ± 10 years, 47% female, 11% short sleepers [< 6 h]). After adjustment for covariates, higher homesickness (β = - 23.19, p < 0.05) and lower civic disengagement (β = 17.75, p < 0.05) were associated with shorter sleep duration in women, while higher isolation was associated with shorter sleep duration in men (β = - 13.73, p < 0.05). Discussion: Results suggest gender-specific associations between acculturative stress and sleep duration. Future research should take into account gender differences in the experience and effects of acculturative stress when developing interventions to improve sleep health in KAIs.
PMID: 31377933
ISSN: 1557-1920
CID: 4015122

Chinese american pain experience (CAPE) project: A mixed-methods study to understand cancer-related pain management in Chinese American patients in new york city [Meeting Abstract]

Kwon, S; Wong, J; Rosenberg, A; Kelly, J; Tong, V; Chong, D; Cuff, G; Chen, Q; Trinh-Shevrin, C
Background: Chinese Americans make up the largest subgroup of the Asian American population in the US and are the largest Asian subset in New York City, where the population of Chinese Americans is 547,886; 72% are foreign-born, 34% lack a high school diploma, 61% have limited English proficiency (LEP), and 21% are living in poverty. Cancer is the leading cause of date among Chinese New Yorkers who suffer a disproportionately high burden for specific cancers, including nasopharyngeal, liver, and stomach cancer. Despite this cancer burden, Chinese Americans are at high risk for poorly controlled and managed pain in clinic and hospital settings and underrepresented in pain related research. The goal of the CAPE project is to understand the concepts of pain and pain experience and identify potential facilitators and barriers to pain treatment and satisfaction among limited-Englishproficient Chinese American inpatients treated at a New York City-based hospital.
Method(s): Kleinman's Patient's Explanatory Model of Illness and principles of social marketing served as guiding frameworks. In addition, a scoping review was conducted of electronic databases including PubMed, Google Scholar, and the gray literature on the pain management literature for Chinese American patients to further inform the interview topic guide and survey instrument. Key search terms included combinations of "Asian American,""Chinese," "Chinese American," "cancer," "pain," "pain management," and "pain experience." Chinese Americanpatients who requested services in Chinese language (e.g., Cantonese, Mandarin) will participate in a one-timequalitative interview and survey data collection. A sample of 25 participants will be recruited or until data saturationis achieved. All data collection will be conducted in the patients' preferred language. Analysis of the qualitative datawill utilize the techniques of narrative analysis and constant comparison analytic approach.
Result(s): The scoping review identified significant gaps in the extant literature. Findings highlighted the lack ofintervention or clinical trial studies to address pain and cancer-related pain management for Chinese Americanpatients despite data confirming high rates of dissatisfaction with pain management in clinic and hospital settings.Qualitative data will be assessed to identify themes related to factors to inform the development of strategies andprograms on optimal and cultural relevant pain management.
Conclusion(s): To improve quality of cancer care for Chinese American patients, study findings will inform thecultural adaption of hospital-based pain management programs and services and practice recommendations tofacilitate culturally relevant pain treatment for this vulnerable patient population
EMBASE:633451777
ISSN: 1055-9965
CID: 4694842