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2.
Community Health Equity Res Policy ; 44(2): 151-163, 2024 Jan.
Article in English | MEDLINE | ID: mdl-36189845

ABSTRACT

BACKGROUND: Despite advances in biomedical HIV prevention modalities such as pre-exposure prophylaxis to prevent the transmission of HIV, racial/ethnic and sexual/gender minority populations are disproportionately impacted by HIV epidemic. Alarming rates of HIV have persisted among Black gay and bisexual men, particularly in Southern states. METHODS: Utilizing data from the ViiV ACCELERATE! initiative, we explored the impact of As Much As I Can, an immersive theatre production, on HIV-related stigma behaviors. A self-administered post-performance survey was conducted with a cohort (n = 322) of randomly selected audience members. RESULTS: Overall, the results showed participants had a highly favorable experience, rating the performance with a mean score of 9.77/10. Respondents indicated they intended to change behaviors to promote HIV prevention education and to reduce stigma and discrimination including: (1) Say something if I hear stigmatizing language against people living with HIV (75.4%), (2) Say something if I hear anti-gay language (69.7%) and (3) Tell others about HIV prevention options (e.g., PrEP, PEP, condoms (64.1%). The findings show there is an association between HIV-related behavior intention and linkage to HIV care. Respondents who reported they were more likely to say something about HIV stigma were almost three times (O.R. 2.77; 95% C.I. 0.98-7.8) more likely to indicate they would follow up with a healthcare professional. CONCLUSIONS: This study suggests that immersive theatre is an effective method for communicating HIV prevention education and reducing HIV-related structural stigma and discrimination that increases HIV vulnerability for Black sexual minority men.


Subject(s)
Art Therapy , Black or African American , HIV Infections , Health Behavior , Health Promotion , Sexual and Gender Minorities , Humans , Male , Black or African American/education , Black or African American/psychology , Black People , Health Promotion/methods , HIV Infections/ethnology , HIV Infections/prevention & control , HIV Infections/psychology , HIV Infections/therapy , Homosexuality, Male/ethnology , Homosexuality, Male/psychology , Medicine in the Arts , Sexual and Gender Minorities/education , Sexual and Gender Minorities/psychology , Sexual Behavior/ethnology , Sexual Behavior/psychology , Social Discrimination/ethnology , Social Discrimination/prevention & control , Social Discrimination/psychology , Social Stigma , Art Therapy/methods , Health Behavior/ethnology
3.
J Behav Med ; 46(6): 1057-1067, 2023 12.
Article in English | MEDLINE | ID: mdl-37392342

ABSTRACT

Discrimination is associated with antiretroviral therapy non-adherence and reduced well-being among people with HIV. We examined the potential for coping to mediate the associations between intersectional discrimination and non-adherence and coping self-efficacy (confidence in one's ability to cope with discrimination) as a moderator that may buffer the negative effects of discrimination on non-adherence in a cross-sectional convenience sample of 82 Latino sexual minority men with HIV. In bivariate linear regressions, discrimination targeting Latino ethnic origin, undocumented residency status, and sexual orientation were each significantly associated with lower self-reported antiretroviral therapy non-adherence (percentage of prescribed doses taken in the last month) and greater use of disengagement coping (denial, substance use, venting, self-blame, behavioral disengagement). Associations between discrimination targeting Latino ethnicity and non-adherence, and discrimination targeting undocumented residency status and non-adherence, were each mediated by disengagement coping responses. Moderation analyses highlighted significant discrimination by coping self-efficacy interaction effects-both coping self-efficacy for problem solving and stopping unpleasant emotions/thoughts each moderated the associations between Latino discrimination and adherence, between undocumented residency status discrimination and adherence, and between HIV discrimination and adherence. Coping self-efficacy for getting social support moderated the association between undocumented residency status discrimination and adherence. Further, the interaction coefficients across models indicated that the negative effects of discrimination on adherence were attenuated at higher levels of coping self-efficacy. Findings highlight the need for structural interventions that reduce-and ultimately eliminate-discrimination, and interventions that address the harmful effects of discrimination and adherence improvement interventions to enhance coping skills among people faced with intersectional discrimination.


Subject(s)
Adaptation, Psychological , HIV Infections , Hispanic or Latino , Medication Adherence , Self Efficacy , Social Discrimination , Humans , Male , Cross-Sectional Studies , Hispanic or Latino/psychology , HIV Infections/drug therapy , HIV Infections/ethnology , HIV Infections/psychology , Social Discrimination/ethnology , Social Discrimination/prevention & control , Social Discrimination/psychology , Medication Adherence/ethnology , Medication Adherence/psychology , Anti-HIV Agents/therapeutic use , Psychological Well-Being/psychology , Sexual and Gender Minorities/psychology , United States/epidemiology
4.
J Health Soc Behav ; 64(4): 593-609, 2023 12.
Article in English | MEDLINE | ID: mdl-37222500

ABSTRACT

Research has consistently linked discrimination and poorer health; however, fewer studies have focused on immigration-related discrimination and mental health outcomes. Drawing on quantitative surveys (N = 1,131) and qualitative interviews (N = 63) with Latino undergraduate students who are undocumented or U.S. citizens with undocumented parents, we examine the association between perceived immigration-related discrimination and mental health outcomes and the process through which they are linked. Regression analyses identify an association between immigration-related discrimination and increased levels of depression and anxiety; this relationship did not vary by self and parental immigration status. Interview data shed light on this result as immigration-related discrimination manifested as individual discrimination as well as vicarious discrimination through family and community members. We contend that immigration-related discrimination is not limited to individual experiences but rather is shared within the family and community, with negative implications for the mental health of undocumented immigrants and mixed-status family members.


Subject(s)
Emigration and Immigration , Hispanic or Latino , Social Discrimination , Students , Undocumented Immigrants , Humans , Hispanic or Latino/psychology , Mental Health , Parents/psychology , Students/psychology , Undocumented Immigrants/psychology , Social Discrimination/ethnology , Social Discrimination/psychology , Family/psychology
5.
J Law Med Ethics ; 51(1): 185-195, 2023.
Article in English | MEDLINE | ID: mdl-37226761

ABSTRACT

This article examines Bey v. City of New York - a recent Second Circuit case where four Black firefights suffering from Pseudofolliculitis Barbae (a skin condition causing irritation when shaving which mostly affects Black men) challenged the New York City Fire Department's Clean Shave Policy - with an intersectional approach utilizing legal theories of racial, disability, and religious discrimination.


Subject(s)
Black People , Firefighters , Folliculitis , Hair Removal , Social Discrimination , Workplace , Humans , Male , Black or African American/legislation & jurisprudence , Black People/legislation & jurisprudence , Firefighters/legislation & jurisprudence , Folliculitis/ethnology , Folliculitis/etiology , Folliculitis/prevention & control , Hair Removal/adverse effects , Hair Removal/methods , New York City , Organizational Policy , Policy , Social Discrimination/ethnology , Social Discrimination/legislation & jurisprudence , Working Conditions/legislation & jurisprudence , Working Conditions/organization & administration , Workplace/legislation & jurisprudence , Workplace/organization & administration
6.
Clin Chest Med ; 44(2): 425-434, 2023 06.
Article in English | MEDLINE | ID: mdl-37085230

ABSTRACT

In the United States, the coronavirus disease-2019 (COVID-19) pandemic has disproportionally affected Black, Latinx, and Indigenous populations, immigrants, and economically disadvantaged individuals. Such historically marginalized groups are more often employed in low-wage jobs without health insurance and have higher rates of infection, hospitalization, and death from COVID-19 than non-Latinx White individuals. Mistrust in the health care system, language barriers, and limited health literacy have hindered vaccination rates in minorities, further exacerbating health disparities rooted in structural, institutional, and socioeconomic inequities. In this article, we discuss the lessons learned over the last 2 years and how to mitigate health disparities moving forward.


Subject(s)
COVID-19 , Health Inequities , Health Services Accessibility , Social Determinants of Health , Social Discrimination , Vulnerable Populations , Humans , Black or African American , COVID-19/epidemiology , COVID-19/ethnology , COVID-19/prevention & control , COVID-19/psychology , Emigrants and Immigrants/psychology , Emigrants and Immigrants/statistics & numerical data , Ethnicity/statistics & numerical data , Health Services Accessibility/economics , Health Services Accessibility/statistics & numerical data , Hispanic or Latino/psychology , Hispanic or Latino/statistics & numerical data , Indigenous Peoples/psychology , Indigenous Peoples/statistics & numerical data , Poverty/ethnology , Poverty/psychology , Poverty/statistics & numerical data , Social Determinants of Health/economics , Social Determinants of Health/ethnology , Social Determinants of Health/statistics & numerical data , Social Discrimination/economics , Social Discrimination/ethnology , Social Discrimination/psychology , Social Discrimination/statistics & numerical data , Social Marginalization/psychology , Trust/psychology , United States/epidemiology , Vaccination/economics , Vaccination/psychology , Vaccination/statistics & numerical data , Vulnerable Populations/psychology , Vulnerable Populations/statistics & numerical data , White/psychology , White/statistics & numerical data
7.
J Immigr Minor Health ; 25(5): 990-998, 2023 Oct.
Article in English | MEDLINE | ID: mdl-36940078

ABSTRACT

South Asians face stressors as a growing immigrant group in America. Work is needed to understand how these stressors impact mental health to identify those at risk of depression and design interventions. This study examined associations of three stressors (discrimination, low social support, limited English proficiency) with depressive symptoms in South Asians. Using cross-sectional data from the Mediators of Atherosclerosis in South Asians Living in America study (N = 887), we fit logistic regression models to evaluate independent/joint effects of three stressors on depression. Overall prevalence of depression was 14.8%; 69.2% of those with all three stressors had depression. The combined effect of high discrimination/low social support was significantly greater than the sum of the individual factors. Experiences of discrimination, low social support, or limited English proficiency, as well as a combination of these factors, should be considered when diagnosing/treating South Asian immigrants in a culturally appropriate manner.


Subject(s)
Depression , Emigrants and Immigrants , Limited English Proficiency , Social Discrimination , Social Support , South Asian People , Humans , Asian , Cross-Sectional Studies , Depression/ethnology , Depression/etiology , Depression/psychology , Emigrants and Immigrants/psychology , Social Support/psychology , South Asian People/psychology , United States , Social Discrimination/ethnology , Social Discrimination/psychology
8.
Ethn Health ; 28(4): 503-521, 2023 05.
Article in English | MEDLINE | ID: mdl-35733281

ABSTRACT

OBJECTIVE: This study used the stress process model to test the mediating effects of personal mastery and moderating effects of church-based social support on the relationship between daily discrimination and psychological distress across three age groups of African American and Afro-Caribbean adults. METHODS: Using a national sample of 5008 African Americans and Afro-Caribbean adults from the National Survey of American Life Study, this study employs structural equation modeling to investigate the relationships between daily discrimination, personal mastery, church-based social support, and psychological distress. RESULTS: Daily discrimination was an independent predictor of psychological distress across all groups. Group- and age-specific comparisons revealed significant differences in the experience of daily discrimination and psychological distress. Mastery was a partial mediator of the relationship between discrimination and psychological distress among Afro-Caribbeans while church support was a significant moderator only among the young and older African Americans. IMPLICATIONS: Together, our study findings provide useful first steps towards developing interventions to reduce the adverse psychological impacts of daily discrimination on African Americans and Afro-Caribbeans. Intervention efforts such as individual psychotherapy aimed to improve Afro-Caribbean individuals' sense of mastery would be a partial solution to alleviating the adverse effects of discrimination on their psychological health.


Subject(s)
Black People , Psychological Distress , Religion and Psychology , Self Efficacy , Social Support , Systemic Racism , Adult , Humans , Age Factors , Black or African American/psychology , Black People/psychology , Mental Health/ethnology , Racism/ethnology , Racism/psychology , Social Discrimination/ethnology , Social Discrimination/psychology , Social Support/psychology , Stress, Psychological/ethnology , Stress, Psychological/etiology , Stress, Psychological/psychology , Systemic Racism/ethnology , Systemic Racism/psychology , United States/epidemiology , Adaptation, Psychological
9.
J Racial Ethn Health Disparities ; 10(4): 1910-1917, 2023 08.
Article in English | MEDLINE | ID: mdl-35876984

ABSTRACT

OBJECTIVES: The purpose of this pilot study was to explore the effect of HIV-related stigma and everyday major experiences of discrimination on medication and clinic visit adherence among older African Americans living with HIV in Ohio. METHODS: We collected data from 53 individuals who were living with HIV in Ohio, ≥ 50 years of age, and who identified as Black or African American. We conducted logistic regression models to examine the impact of HIV-related stigma and experiences of discrimination on medication and visit adherence. Each model controlled for age, time since diagnosis, and sexual orientation. RESULTS: The average age was 53.6 ± 2.1 years and 94.3% were men. Almost half (49.1%) of the participants reported poor medication adherence and almost a third (31.4%) reported poor visit adherence. HIV-related stigma (adjusted odds ratio (aOR) = 1.39; 95% confidence interval (CI) = 1.02-1.89) and major experiences of discrimination (aOR = 1.70; 95% CI = 1.11-2.60) were associated with a greater odds of poor medication adherence. Additionally, major experiences of discrimination were associated with a threefold increase in the odds of poor visit adherence (aOR = 3.24; 95% CI = 1.38-7.64). CONCLUSIONS: HIV-related stigma and major experiences of discrimination impede optimal medication and HIV clinic visit adherence for older African Americans living with HIV. To reduce the impact of stigma and discrimination on HIV care engagement, our first step must be in understanding how intersecting forms of stigma and discrimination impact engagement among older African Americans living with HIV.


Subject(s)
Ambulatory Care , Black or African American , HIV Infections , Patient Compliance , Social Discrimination , Social Stigma , Female , Humans , Male , Middle Aged , Black or African American/psychology , Black or African American/statistics & numerical data , Black People/psychology , Black People/statistics & numerical data , HIV Infections/epidemiology , HIV Infections/ethnology , HIV Infections/psychology , HIV Infections/therapy , Medication Adherence/ethnology , Medication Adherence/psychology , Medication Adherence/statistics & numerical data , Pilot Projects , Ohio/epidemiology , Patient Compliance/ethnology , Patient Compliance/psychology , Patient Compliance/statistics & numerical data , Ambulatory Care/psychology , Ambulatory Care/statistics & numerical data , Racism/ethnology , Racism/psychology , Racism/statistics & numerical data , Social Discrimination/ethnology , Social Discrimination/psychology , Social Discrimination/statistics & numerical data
10.
J Am Geriatr Soc ; 70(2): 592-600, 2022 02.
Article in English | MEDLINE | ID: mdl-35015300

ABSTRACT

In addition to numerous care responsibilities, family caregivers are expected to navigate health systems and engage in healthcare management tasks on behalf of their persons living with dementia (PLWD). These challenging tasks pose additional difficulties for Black dementia caregivers. Due to the centuries-old, disadvantaged social history of Black Americans, several unique stressors, vulnerabilities, and resources have emerged which inform and affect Black dementia caregivers' experiences and well-being. Focus groups were held with Black caregivers (N = 19) from the United States to explore the unique experiences and perspectives of this population navigating the U.S. health system on behalf of their PLWD. Five overarching themes were constructed during thematic analysis: Forced Advocacy, Poor Provider Interaction, Payor Source Dictates Care, Discrimination, and Broken Health System. Black dementia caregivers unanimously concurred that the health system that they experience in America is "broken." Gaps in the health system can lead to people [as one caregiver passionately expressed] "falling between the cracks," in terms of care, services, and resources needed. Caregivers agreed that class, sex, utilizing public health insurance, and being a "person of color" contribute to their difficulties navigating the health system. Caregivers perceived being dismissed by providers, forcing them to advocate for both themselves and their PLWD. Healthcare providers and researchers can utilize these findings to improve the experiences and healthcare outcomes of Black persons living with dementia and their caregivers. Additionally, these findings can lead to the development of culturally tailored caregiver education programs.


Subject(s)
Black People/statistics & numerical data , Caregivers/statistics & numerical data , Delivery of Health Care/ethnology , Dementia/nursing , Focus Groups , Health Services Accessibility , Humans , Middle Aged , Reimbursement Mechanisms/economics , Social Discrimination/ethnology , United States
12.
J Acad Nutr Diet ; 121(9): 1679-1694, 2021 09.
Article in English | MEDLINE | ID: mdl-34294591

ABSTRACT

BACKGROUND: A steep rise in food insecurity is among the most pressing US public health problems that has resulted from the COVID-19 pandemic. OBJECTIVE: This study aimed to (1) describe how food-insecure emerging adults are adapting their eating and child-feeding behaviors during COVID-19 and (2) identify barriers and opportunities to improve local food access and access to food assistance. DESIGN: The COVID-19 Eating and Activity Over Time study collected survey data from emerging adults during April to October 2020 and completed interviews with a diverse subset of food-insecure respondents. PARTICIPANTS/SETTING: A total of 720 emerging adults (mean age: 24.7 ± 2.0 years; 62% female; 90% living in Minnesota) completed an online survey, and a predominately female subsample (n = 33) completed an interview by telephone or videoconference. MAIN OUTCOME MEASURES: Survey measures included the short-form of the US Household Food Security Survey Module and 2 items to assess food insufficiency. Interviews assessed eating and feeding behaviors along with barriers to healthy food access. ANALYSES PERFORMED: Descriptive statistics and a hybrid deductive and inductive content analysis. RESULTS: Nearly one-third of survey respondents had experienced food insecurity in the past year. Interviews with food-insecure participants identified 6 themes with regard to changes in eating and feeding behavior (eg, more processed food, sporadic eating), 5 themes regarding local food access barriers (eg, limited enforcement of COVID-19 safety practices, experiencing discrimination), and 4 themes regarding barriers to accessing food assistance (eg, lack of eligibility, difficulty in locating pantries). Identified recommendations include (1) expanding the distribution of information about food pantries and meal distribution sites, and (2) increasing fresh fruit and vegetable offerings at these sites. CONCLUSIONS: Interventions of specific relevance to COVID-19 (eg, stronger implementation of safety practices) and expanded food assistance services are needed to improve the accessibility of healthy food for emerging adults.


Subject(s)
COVID-19/epidemiology , Diet/standards , Food Assistance/standards , Food Insecurity , Adult , Ethnicity , Feeding Behavior , Female , Humans , Male , Minnesota/epidemiology , Prevalence , Racism/ethnology , SARS-CoV-2 , Social Discrimination/ethnology , Socioeconomic Factors , Young Adult
15.
JAMA Netw Open ; 4(1): e2033484, 2021 01 04.
Article in English | MEDLINE | ID: mdl-33394004

ABSTRACT

Importance: Violence is a significant public health problem that has become entwined with the coronavirus disease 2019 (COVID-19) pandemic. Objective: To describe individuals' concerns regarding violence in the context of the pandemic, experiences of pandemic-related unfair treatment, prevalence of and reasons for firearm acquisition, and changes in firearm storage practices due to the pandemic. Design, Setting, and Participants: This survey study used data from the 2020 California Safety and Well-being Survey, a probability-based internet survey of California adults conducted from July 14 to 27, 2020. Respondents came from the Ipsos KnowledgePanel, an online research panel with members selected using address-based sampling methods. Responses were weighted to be representative of the adult population of California. Main Outcomes and Measures: Topics included worry about violence for oneself before and during the pandemic; concern about violence for someone else due to a pandemic-related loss; experiences of unfair treatment attributed to the pandemic; firearm and ammunition acquisition due to the pandemic; and changes in firearm storage practices due to the pandemic. Results: Of 5018 invited panel members, 2870 completed the survey (completion rate, 57%). Among respondents (52.3% [95% CI, 49.5%-55.0%] women; mean [SD] age, 47.9 [16.9] years; 41.9% [95% CI, 39.3%-44.6%] White individuals), self-reported worry about violence for oneself was significantly higher during the pandemic for all violence types except mass shootings, ranging from a 2.8 percentage point increase for robbery (from 65.5% [95% CI, 62.8%-68.0%] to 68.2% [95% CI, 65.6%-70.7%]; P = .008) to a 5.6 percentage point increase for stray bullet shootings (from 44.5% [95% CI, 41.7%-47.3%] to 50.0% [47.3%-52.8%]; P < .001). The percentage of respondents concerned that someone they know might intentionally harm themselves was 13.1% (95% CI, 11.5%-15.3%). Of those, 7.5% (95% CI, 4.5%-12.2%) said it was because the other person had experienced a pandemic-related loss. An estimated 110 000 individuals (2.4% [95% CI, 1.1%-5.0%] of firearm owners in the state) acquired a firearm due to the pandemic, including 47 000 new owners (43.0% [95% CI, 14.8%-76.6%] of those who had acquired a firearm). Of owners who stored at least 1 firearm in the least secure way, 6.7% (95% CI, 2.7%-15.6%) said they had adopted this unsecure storage practice in response to the pandemic. Conclusions and Relevance: In this analysis of findings from the 2020 California Safety and Well-being Survey, the COVID-19 pandemic was associated with increases in self-reported worry about violence for oneself and others, increased firearm acquisition, and changes in firearm storage practices. Given the impulsive nature of many types of violence, short-term crisis interventions may be critical for reducing violence-related harm.


Subject(s)
Anxiety/epidemiology , COVID-19 , Social Discrimination/statistics & numerical data , Violence/psychology , Adult , Black or African American , Anxiety/psychology , Asian , California/epidemiology , Commerce , Fear/psychology , Female , Firearms/statistics & numerical data , Hispanic or Latino , Humans , Internet , Male , Middle Aged , Ownership , Police , SARS-CoV-2 , Safety , Social Discrimination/ethnology , Surveys and Questionnaires , White People
16.
Cyberpsychol Behav Soc Netw ; 23(12): 865-870, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32762541

ABSTRACT

Since the outbreak of COVID-19, Asians and Asian Americans have been experiencing an uptick of discrimination. With most people experiencing months of lockdowns, social media may become a particularly important tool in Asian people's coping with discrimination. Grounded in the multiactivity framework of social media use, this study explored whether experience with discrimination was associated with more social media use among Asian people and how adaptive social media use was for their well-being during COVID-19. A sample of 242 Asians/Asian Americans residing in the United States (Mage = 32.88, SD = 11.13; 48 percent female) completed an online survey. Results showed that more experience of discrimination during COVID-19 was associated with more engagement in social media private messaging, posting/commenting, and browsing, but the activities yielded different implications for subjective well-being. Both social media private messaging and posting/commenting were associated with more perceived social support, which contributed to better subjective well-being. Social media posting/commenting was also related to better subjective well-being through lower worry about discrimination. In contrast, social media browsing was associated with poorer subjective well-being through more worry about discrimination.


Subject(s)
Asian/psychology , COVID-19 , Quarantine/psychology , Social Discrimination/ethnology , Social Media , Adaptation, Psychological , Adult , COVID-19/prevention & control , Female , Humans , Male , SARS-CoV-2 , Social Support , Surveys and Questionnaires , United States
17.
Psychiatry Res ; 291: 113203, 2020 09.
Article in English | MEDLINE | ID: mdl-32559671

ABSTRACT

Mental-health problems are common among older adults, especially those who are members of disadvantaged ethnic minorities. We explored ethnic and gender differences in emotional distress, perceived discrimination, and self-esteem among elderly Bedouin Arab and Jewish individuals in Israel, as well as the moderating role of discrimination in the association between self-esteem and emotional distress among Bedouin Arabs. The sample included 256 older adults (60 years old and above): 147 native-born Israeli Jews and 109 Bedouin Arabs. Participants completed self-report questionnaires that assessed emotional distress, perceived discrimination, self-esteem, and sociodemographic factors. Israeli Jews reported lower levels of emotional distress than Bedouin Arabs. Bedouin Arab women reported more emotional distress than Bedouin Arab men. Among the Bedouin Arabs, gender differences were found in the associations of perceived discrimination and self-esteem with emotional distress. Among the Bedouin men, discrimination and self-esteem were found to be significant predictors of emotional distress. Among the Bedouin women, we found a similar association between self-esteem and emotional distress. However, the protective role of self-esteem disappeared in the context of higher levels of daily discrimination. This study underscores how gender can affect the moderating role of discrimination in the association between self-esteem and emotional distress among the elderly.


Subject(s)
Arabs/psychology , Jews/psychology , Psychological Distress , Self Concept , Sexism/psychology , Social Discrimination/psychology , Age Factors , Aged , Aged, 80 and over , Cross-Cultural Comparison , Female , Humans , Israel/ethnology , Male , Middle Aged , Minority Groups/psychology , Role , Sexism/ethnology , Social Discrimination/ethnology , Surveys and Questionnaires
18.
Perspect Psychol Sci ; 15(4): 1131-1139, 2020 07.
Article in English | MEDLINE | ID: mdl-32324488

ABSTRACT

A strong preference for fair skin appears to be the norm across the Asian continent and may pervade many aspects of social life. Yet scholarly work on this ubiquitous phenomenon is rare within psychological science. This article is a call for a psychological investigation into colorism in Asia. I argue that colorism has firm systemic roots as a result of the sociohistorical trajectories of different Asian societies that have attached cultural meanings to skin color. Consequently, similarities and differences in such trajectories may account for variability in the expression of colorism within contemporary Asian societies. Directions for a cultural psychological approach to colorism are suggested.


Subject(s)
Colonialism , Psychology , Skin Pigmentation , Social Discrimination/ethnology , Asia/ethnology , Humans , Racism/ethnology
19.
Ethn Dis ; 30(2): 261-268, 2020.
Article in English | MEDLINE | ID: mdl-32346271

ABSTRACT

Objectives: African Americans face challenges in accessing services for sexually transmitted infections (STIs). From 2012-2016, the EBAN II intervention was funded by the NIH to test the effectiveness of implementing a culturally congruent, evidence-based HIV/AIDS prevention program in Los Angeles and Oakland, California. This study examined the impact of personal characteristics and experiences of discrimination on the likelihood of being tested for STIs. Methods: Participants (N=91) completed a baseline survey. Descriptive statistics were used to test for differences between those who did and did not obtain STI testing. Factors included HIV serostatus, sociodemographic variables, STI history, the presence of outside partners, and discrimination experiences. Multiple logistic regressions were conducted for men and women separately. Results: Participants with no recent experiences of discrimination were more than 3 (3.4) times more likely to obtain a baseline STI test than those who reported discrimination experiences. HIV-positive women with no recent experiences of discrimination were 11 times more likely than those with reports of recent discrimination to obtain STI tests. Conclusions: It is often women who are the gatekeepers for health seeking in families and the same may be for these couples. Experiences of discrimination may impede STI testing, and heighten several health risks, particularly among HIV-positive African American women in HIV-serodiscordant relationships. Addressing the impact of discrimination experiences may be important for STI prevention and treatment efforts in interventions promoting health care utilization.


Subject(s)
Black or African American , Communication Barriers , HIV Infections/diagnosis , Sexually Transmitted Diseases , Social Discrimination , AIDS Serodiagnosis , Adult , Black or African American/psychology , Black or African American/statistics & numerical data , Female , Humans , Los Angeles/epidemiology , Male , Patient Acceptance of Health Care , Sexual Partners/psychology , Sexually Transmitted Diseases/ethnology , Sexually Transmitted Diseases/prevention & control , Sexually Transmitted Diseases/psychology , Social Discrimination/ethnology , Social Discrimination/prevention & control , Social Discrimination/psychology
20.
Ann Epidemiol ; 45: 32-39, 2020 05.
Article in English | MEDLINE | ID: mdl-32340835

ABSTRACT

PURPOSE: The aim of the study was to quantify the association between perceived everyday discrimination and binge eating among Latinas in the United States. METHODS: Participants included 1014 Latinas from the 2002-2003 National Latino and Asian American Study. Modified Poisson models with robust standard errors were used to estimate sociodemographic-adjusted prevalence ratios (aPRs) and 95% confidence intervals (CIs) of binge eating associated with overall and attribution-specific discrimination. RESULTS: Approximately 7% of Latinas reported binge eating. Increased frequency of discrimination was associated with a higher prevalence of binge eating (aPR, 1.59; 95% CI, 1.23-2.06), and Latinas reporting frequencies of discrimination in the top tertile had the greatest prevalence elevation (aPR, 3.63; 95% CI, 1.32-10.00). There were important differences by discrimination attribution: Latinas experiencing primarily height/weight-based or skin color-based discrimination had the greatest prevalence elevation relative to those reporting no discrimination (aPR, 10.24; 95% CI, 2.95-35.51; and aPR, 8.83; 95% CI, 2.08-37.54, respectively), whereas Latinas reporting primarily race-based discrimination had the lowest prevalence elevation (aPR, 1.64; 95% CI, 0.47-5.69). CONCLUSIONS: Discrimination may be an important social determinant of Latinas' binge eating. Future research should incorporate expanded conceptual models that account for Latinas' complex social environment, focusing on intersecting dimensions of identity.


Subject(s)
Binge-Eating Disorder/psychology , Bulimia/psychology , Hispanic or Latino/psychology , Obesity/psychology , Racism/psychology , Social Discrimination/psychology , Acculturation , Adult , Binge-Eating Disorder/complications , Body Mass Index , Body Weight , Bulimia/ethnology , Female , Health Status Disparities , Hispanic or Latino/statistics & numerical data , Humans , Male , Middle Aged , Prevalence , Residence Characteristics , Social Discrimination/ethnology , Social Environment , United States/epidemiology
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