Abstract
Stress and distress among immigrant communities in the United States have escalated under the recent sociopolitical climate (e.g., exclusionary federal policies, COVID-19), underscoring the urgent need for additional data to better understand immigrant experiences. Yet, the very stressors that generate this need for data also create fear and trust-related barriers that might impede research success. Barriers, including a lack of trust, power differentials, language differences, and varying cultural norms, negatively impact the collection of valid data. Recommendations to address these barriers are provided, and integration of such strategies is an essential step toward growing the knowledge base of the profession, delivery of evidence-based interventions with immigrant clients, and better-informed discussions of culturally responsive approaches in social work education and practice.
An estimated 45 million immigrants reside in the United States, accounting for about 15% of the population (Budiman, 2020; USAFacts, 2019). Immigration can be a challenging endeavor that places individuals in vulnerable positions once in the destination country, regardless of country of origin or motive for moving (Zaheer et al., 2018). In response, social workers have a long history of engaging with immigrant community members through direct service provision and advocacy (National Association of Social Workers [NASW], n.d.). The service concerns of immigrant clients have shifted in recent years as immigrants have experienced changing needs associated with COVID-19 and punitive and exclusionary federal policies, resulting in increased levels of stress (Asad, 2020; Held et al., 2018, 2020; Lipka, 2017; Rai et al., 2020; Torres et al., 2018). These changes underscore an urgent need to gain additional data to better understand immigrant experiences. Yet, the very stressors that generate this need for current data also create fear and trust-related barriers that might impede research success (Lahman et al., 2011; Olukotun & Mkandawire-Valhmu, 2020).
Existing literature provides valuable context related to conducting research with vulnerable and hidden communities (Ellard-Gray et al., 2015; United Nations Women, 2020), though fewer guidelines are available specific to the recent sociopolitical context. Given the vulnerability of immigrants in the United States along with their unique positionality, this discussion is vital. This brief draws from immigrant researchers’ experiences in the United States to discuss barriers relating to both research participation and valid data collection, in addition to delineating strategic recommendations for addressing these barriers.
Recent Anti-Immigrant Sentiment and Policies in the United States
Immigrant communities have endured excessive stress in recent years associated with anti-immigrant sentiments and COVID-19 (Chishti & Bolter, 2020; Fogel, 2021), yet simultaneously demonstrated resilience (Jones et al., 2021; United Nations, 2020). Anti-immigrant sentiments are visible in both the elevation of xenophobic behaviors and rhetoric (e.g., “build the wall,” the “Muslim Ban,” and the “Chinese virus”), as well as exclusionary immigration policies under former President Trump that instill fear of foreigners and perpetuate hate crimes against diverse immigrant groups (Gover et al., 2020; Moreno, 2020; United Nations, 2020). Exclusionary immigration policies are deeply harmful, as exemplified through separation of Latinx families at the southern border, deportation, and entry bans into the United States (de la Peña et al., 2019; Hackman, 2020). In Fiscal Year 2019, 143,000 adult immigrants were detained and 267,000 were deported (Department of Homeland Security, 2021).
More recently, some groups, such as Asian immigrants have been scapegoated for the spread of the COVID-19 virus (Chishti & Bolter, 2020). Acts of xenophobia may have heightened due to the racist remarks by former President Trump by referring to COVID-19 virus as, “Kung flu” or the “Chinese virus” (Chiu, 2020; Gover et al., 2020; Moreno, 2020; Müller & Schwartz, 2020). Examples of such hate crimes include anti-Muslim mosque attacks, a mass shooter targeting “Mexicans” at a shopping center in El Paso, and the killing of women of Asian descent at multiple spas in Atlanta, among other incidents, all testament to the increasing hate and the incrimination of immigrant communities (American Civil Liberties Union [ACLU], 2021; Campbell, 2019; New York Times, 2021).
Visa holders, who are at lower risk of detention or deportation, have still been impacted by recent policies (Rai et al., 2020). Furthermore, immigrants who possess H-1B (temporary employment) visas and H-4 (dependents of H-1B visa holders) visas have experienced added stress during the pandemic under President Trump’s administration. In addition to employment-related challenges associated with revocation of work permissions (Bloomberg, 2020), a recent ban implemented under the Trump administration prevented new H-1B visas from being granted until March 31, 2021 (Hackman, 2020). This order not only caused financial loss to families, but also enhanced stress and separation of family members (Parvini, 2020; Rai et al., 2020).
In addition to exclusionary policies, a recent stressor that disproportionately impacts immigrants is the pandemic. Immigrants are overrepresented in certain frontline coronavirus-response occupations, such as in health care professions where they comprise 29% of all physicians and 38% of home health aides (Gelatt, 2020). While a proportion of immigrants face greater risk of contracting COVID-19 through work, another segment of immigrants has been forced out of work due to the stay-at-home orders and mass layoffs (Chishti & Bolter, 2020; Gelatt, 2020). Moreover, most immigrants with legal documentation status and United States citizen spouses of unauthorized immigrants will be ineligible for pandemic aid packages provided by the federal government (Gelatt, 2020), and most immigrants are already ineligible for existing public safety nets (e.g., food stamps) due to the Personal Responsibility and Work Opportunity Reconciliation Act of 1996 (U.S. Department of Health & Human Services, 1996).
Stress associated with both anti-immigrant sentiment and COVID-19 can be significantly detrimental to mental health outcomes, worsening risk of depression, anxiety, and posttraumatic stress disorder (PTSD) (Bennett et al., 2020; Lincoln et al., 2020; Salas-Wright et al., 2020). Yet, even in the face of such stress, immigrants have displayed individual- and community-level resilience, which can help to buffer the harmful effects of stress on mental health (Akinsulure-Smith, 2017; Choi et al., 2020). Gaining in-depth insight into the experiences of both stress and resilience are essential to informing social work education, micro- and macro-level practice, and future research directions. The current context, however, has created an atmosphere of fear in which immigrant communities might be disinclined to engage in research or to share their experiences. The following brief overviews barriers and strategic recommendations for establishing trust and collaborations to build the research base which can strengthen social work education and practice in an ethical and responsible way.
Barriers to Research Success
Multiple barriers exist for recruitment and valid data collection when conducting research with immigrant populations, including limited trust of researchers, power differentials, language differences, and varying cultural norms (Forrest-Bank et al., 2019; Scharff et al., 2010; Yick, 2007). Each of these factors can individually affect research, though many immigrants may encounter multiple barriers.
Lack of Trust
Vulnerable communities have numerous reasons to mistrust researchers. A lack of trust may stem from historical horrific and blatant abuse, like renowned cases such as the Tuskegee syphilis study (Centers for Disease Control and Prevention [CDC], 2021a), but it is also reinforced by a range of other factors, including discriminatory institutional practices encountered daily by members of these communities (Scharff et al., 2010). Trust can also be severed when researchers fail to verify their findings or report back results to those who devoted time to a study (Pittaway et al., 2010; Yuan et al., 2016). Furthermore, researchers might come from outside the cultural communities they are examining and could easily misrepresent participants in their well-intentioned, though misinformed presentation of findings (Suárez-Orozco & Carhill, 2008).
As a response to Tuskegee, the 1974 National Research Act created the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, the first public national body to assist in the formation of bioethics policy in the United States (CDC, 2021b; President’s Council on Bioethics, n.d.). This led to the establishment of ethical principles for the protection of human subjects in research (e.g., respect for persons, beneficence, and justice) in the Belmont Report and suggested methods to ensure these principles are followed (e.g., Institutional Review Boards) (CDC, 2021b). The application of these principles in research (e.g., informed consent and confidentiality) carry great significance for members of immigrant populations. For example, researchers must be aware of considerations of deportation and detention when working with immigrants and going above and beyond to maintain confidentiality is crucial to build trust with participants concerned about immigration status (Suárez-Orozco & Yoshikawa, 2013). Immigrants who are identified by immigration enforcement can face risk of detention or deportation, resulting in temporary or permanent separation from loved ones while also being forced to return to a hazardous situation in their home countries (Stillman, 2018). Doran et al. (2018) discuss how despite following best practices for research with Latinx communities (e.g., inclusion of bilingual Latinx research assistants and study materials back translated into Spanish), refusal rates for participation in their study was higher among Latinx than non-Latinx individuals due to concerns regarding immigration status.
There is no doubt that the effects associated with immigration enforcement are prominent and dire (American Psychological Association, 2018; Gulbas et al., 2016; Potochnick et al., 2017). Lack of trust can influence any step of a research project, from fear of being identified as an immigrant and being asked to answer invasive questions to fear that someone in their community might be identified through the dissemination of findings (Kass et al., 1996; Mastroianni, 2008). Saasa et al. (2021) modified their question around immigration status to ask participants about how they entered the United States rather than asking them about their visa type to encourage participation. Similar questions can be employed in research with immigrants.
Power Differentials
Recognizing the systemic oppression and disempowerment of their communities, some immigrants may see research as a way to highlight their circumstances to those in positions of power and potentially influence public policy (Raymond-Flesch et al., 2016). However, researchers, even those who collaborate with community members in the design of a study, may conduct research more with a focus on advancing the discipline than on the needs of the community (Nyden & Wiewel, 1992). Differing perceptions of researchers and the authority that they hold can be informed by culture and prior experiences (Fontes, 1998). For example, Asian American immigrants deliberating consent to participate in a study on domestic violence may not feel comfortable declining due to the power differential between themselves and the researcher given their minority status, possible immigration status, and gender differences, if the researcher is male (Yick, 2007).
Language Differences
Linguistic differences between participants and researchers can pose multiple challenges. Languages from nearly every nation are represented among immigrant communities in the United States (Budiman, 2020). Though some standardized measures are validated in multiple languages, a large number are either only available in English or a small set of other languages (Beaton et al., 2000; Guillemin et al., 1993). Translating documents is a complex and intensive process that is made more arduous by the same language being spoken in varying dialects across countries and regions (Kamla & Komori, 2018; Pena, 2007; Regmi et al., 2010). Even when translating a document into a commonly spoken language in the United States, such as Spanish, Held (2018) has found that native speakers from different countries might suggest differing terms or phrases as Spanish-speaking communities are diverse. The resultant survey or interview questions, then, might fail to fully convey the intended meaning. Rai (2021) back translated a research survey in Hindi, a commonly spoken South Asian language to encourage participation in a study on domestic violence. In addition to back translation, the author culturally adapted the survey to encourage community participation by ensuring the questions were culturally appropriate.
Varying Cultural Norms
Even more concerning is that once measures are validated in a given language, researchers might be inclined to use the measure without thoroughly vetting the cultural implications for diverse participant communities or research objectives (Agha & Rai, 2020). Constructs, such as domestic violence and mental health conditions, can be conceptualized differently across cultures (Forrest-Bank et al., 2019; Rai & Choi, 2021). For instance, researchers studying domestic violence in immigrant populations continue to use scales such as the Conflict Tactics Scale (Straus et al., 1996), which may not capture the unique tactics of violence in immigrant families such as abuse by in-laws (Agha & Rai, 2020; Rai & Choi, 2021; Rai et al., 2020). In response, some immigrant community members might perceive their experiences to be irrelevant to the project itself and drop out of the study. For example, individuals who understand symptoms of depression or trauma through a non-Western lens might not understand the researchers’ intended meaning of the study or how it could relate to their experiences (Renner et al., 2006). Attempting to utilize measures to accurately capture a construct in a way that both participants and researchers understand the meaning can be a toiling process without a guaranteed positive outcome.
Strategic Recommendations
With a heightened, immediate need to better understand immigrant experiences related to increasing anti-immigrant sentiments and COVID-19, reaching these communities utilizing ethical and culturally responsible research strategies is essential (Martinez et al., 2008; Rai et al., 2020). The following strategies are presented to engage specifically with immigrant communities as a means of growing the knowledge base that can directly strengthen social work education, practice, and future research agendas: community-based partnerships, best practices in language translation, protection of information, and intentional consideration of what can be provided back to the community.
Community-Based Partnerships
In a review of the literature, Vaughn et al. (2017) noted that immigrant involvement in community-based participatory research (CBPR) appears to be a recent but growing trend and cited benefits to the research (e.g., increased recruitment, improved quality) and to immigrants themselves (e.g., empowerment, development of new skills). Establishing partnerships with key stakeholders, such as community-based organization providers, faith-based leaders, advocacy groups, youth leaders, and community leaders, is an essential and multifaceted step that can aid in overcoming the mistrust that is fostered by the current sociopolitical context that criminalizes and oppresses immigrants (Gover et al., 2020; Woods-Jaeger et al., 2021).
Partnering with the community provides recognition that knowledge exists both in academia and the local community (Hacker, 2017), knowledge which can be critical to informing all elements of a study, including conceptualization, design, and interpretation of findings. Ferrera et al. (2015) describe how CBPR was utilized to assess a youth health education program targeting marginalized immigrants in Chicago. Mindful of societal power differentials and maintaining an equitable partnership, researchers collaborated with community partners to determine research goals, design the questionnaire, outline the data collection process and translate findings into community-relevant interventions and policies (Ferrera et al., 2015). Chang et al. (2013) discuss how trust building between university and community partners, and eventually with the broader community, was key to improving research participation of vulnerable immigrant restaurant workers to report substandard work conditions.
CBPR builds on the strengths and resources that are located within the community (Hacker, 2017), as local stakeholders can provide insight into concerns the community holds, valuable translation and interpretation assistance due to possible language expertise, strategies for gaining trust and for recruitment, and relevant insight about potential historical trauma relevant to the specific community (Nguyen-Truong et al., 2018). CBPR advocates research practices that engage community stakeholders in a way that fosters mutual respect and trust, helping to further social justice by sharing power and empowering communities (Hacker, 2017). The empowerment of communities by inviting community stakeholders to co-present findings at conferences or help create innovative avenues for dissemination within the community, enriches the discourse and encourages practical application of research findings (Chang et al., 2013).
Best Practices in Language Translation
Research with immigrant communities necessitates linguistically and culturally appropriate strategies that allow participants to complete research activities in their preferred language to promote meaningful participation and more accurate responses (Childs et al., 2014; Dobrin & Schwartz, 2016). While ethical practices around language are always a requisite among researchers, demonstrating a clear dedication to linguistic needs carries additional benefits of reflecting researchers’ intentions, respect, and humility in the current exclusionary immigration policy environment.
A rigorous process of translation—back translation (Tyupa, 2011; World Health Organization, 2021) is the first step to ensuring accuracy of language and is reflected within the body of research with immigrant communities (Held, 2018; Mahapatra, 2008; Rai, 2021). Subsequent steps that can be employed are having native language-speaking providers and other stakeholders review documents for accuracy and preferred wording (Chen & Boore, 2010; Jones et al., 2001). Finally, piloting study questions and measures before fully launching the project can provide another check of accuracy (Martinez et al., 2008; Streiner & Norman, 1995).
Gaining input from immigrants who speak the relevant language but are from different countries and/or regions can be valuable (Jones et al., 2001). Varying cultural norms across communities may attribute different meanings to a social issue. For instance, having conversations about domestic violence may be a taboo in the South Asian immigrant community (Rai & Choi, 2021), but an engaged dialogue around healthy relationships may be welcomed by members of this immigrant group. Culturally unresponsive research or the use of instruments that are not sensitive to the cultures of diverse communities may discourage participation (Agha & Rai, 2020; White et al., 2013). Therefore, it is imperative for researchers to understand the cultural nuances of communities they are interested in learning about or supporting through their research efforts.
Protection of Information
While many immigrant participants can fear identification when participating in research, this fear might be elevated with the increased anti-immigrant sentiment and xenophobia in the United States today (Chishti and Bolter, 2020; Rai et al., 2020). Furthermore, undocumented immigrants are at particular risk associated with immigration enforcement. This segment of immigrants continuously lives under the radar to avoid risk of identification, which can lead to detention and deportation (Artiga & Ubri, 2017; Held et al., 2020; Martinez et al., 2008). As a result, not only protecting participant information but also ensuring that participants fully understand these protections is pertinent in this highly punitive immigration policy environment. As discussed earlier, there can be a detrimental power differential among researchers and community member participants (Yick, 2007), which might be even more pronounced in research with immigrants (Hernández et al., 2013). By ensuring adequate and responsible protection of information and participant interests, researchers can minimize this differential and encourage immigrant participants to be engaged in research endeavors (Karnieli-Miller et al., 2009).
In addition to standard protections of data, researchers can take extra steps to reduce risk and fear associated with participant identification when conducting studies with immigrants. One step is through excluding questions that ask about name, date of birth, and related identifying information or protecting that information when collecting it is essential to the study, a vital step toward reducing fear of participation (Hernández et al., 2013). In addition, avoiding collection of signed consent forms is another step toward protecting identity to eliminate fear of names being associated with the study in any way. Moreover, emphasizing that participation is voluntary and that participants can respond to the questions to the extent they are comfortable is not only required as a component of the Belmont Report (U.S. Department of Health & Human Services, 1979) but might also be imperative to immigrant participants feeling safe.
Intentional Consideration of What Can be Provided to the Community
Researchers must provide participants the opportunity to honestly share their responses as well as make efforts to compensate participants for their time (Cheff, 2018). Asking key stakeholders about best ways to support the community can be a valuable starting point to learning how to intentionally give back. In the experiences of the authors, some organizations are severely short-staffed and can profit most from a researcher volunteering to support direct service efforts. In other settings, the authors have experienced providers requesting trainings or reports of already existing data to inform their work. Ultimately, researchers have the unique opportunity to not only design and collect data for studies that are well informed by the community but to also meaningfully give back to those participating in research.
Implications for Practice
Remarks about “illegal immigration” and frequent changes in visa regulations by former President Trump has instilled fear among immigrants (Chishti & Bolter, 2020). Blaming the Asian community for spreading the virus or calling it the “Chinese virus” has enhanced xenophobia in America (Gover et al., 2020; Moreno, 2020). Overcoming the mistrust and fear associated with this oppressive context is challenging but imperative to learn more about immigrant communities and strategies for improving support and service provision. Research that utilizes strategies, like the ones presented here, can benefit practitioners working to support the unique vulnerabilities and resiliencies of their immigrant clients. Furthermore, culturally responsive data generated through research can assist practitioners in better understanding and meeting the needs of their immigrant clients. Through collaborations among researchers, providers, and immigrant communities, a stronger body of research can be established to inform not only future research directions but also best practices for serving immigrant communities. Social work educators are also encouraged to adequately engage in discussing culturally responsive approaches and why they are needed so students are aware of current limitations in research and feel better prepared to engage with immigrant communities.
Conclusion
Multiple barriers exist to research participation and valid data collection with immigrant communities, which, ultimately, may impact the culturally informed care practitioners strive to provide. These barriers are even more pronounced when immigrant communities are contending with elevated rates of punitive immigration policies, discrimination, and xenophobia that has been present at federal and local policy levels, as well as among the general public. This research brief delineates barriers and nuanced strategies to improve research participation and valid data collection with diverse immigrant communities in the current and emerging sociopolitical context. Employing these strategies can serve as an essential step toward continuously improving the body of research that supports provider organizations in delivering evidence-informed interventions and service. Moreover, further conversations and deliberations on considering innovative approaches of engaging with immigrant participants are needed. Although researchers may already be familiar with one or several of the provided recommendations, more can, and should, be done to improve the collection of valid data and better support the needs of this significant and essential population.
Footnotes
Disposition editor: Sondra J. Fogel
Declaration of Conflicting Interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The author(s) received no financial support for the research, authorship, and/or publication of this article.
