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Transformative Research and Ethics
In: The Handbook of Social Research Ethics
By: Donna M. Mertens, Heidi M. Holmes & Raychelle L. Harris
Edited by: Donna M. Mertens & Pauline E. Ginsberg
Pub. Date: 2013
Access Date: October 7, 2019
Publishing Company: SAGE Publications, Inc.
City: Thousand Oaks
Print ISBN: 9781412949187
Online ISBN: 9781483348971
DOI: https://dx.doi.org/10.4135/9781483348971
Print pages: 85-102
© 2009 SAGE Publications, Inc. All Rights Reserved.
This PDF has been generated from SAGE Research Methods. Please note that the pagination of the
online version will vary from the pagination of the print book.
Transformative Research and Ethics
Donna M.Mertens, Heidi M.Holmes and Raychelle L.Harris
What are the ethical implications of pouring millions of dollars into research and producing volumes of
articles on critical social problems such as HIV/AIDS or literacy if the epidemics of disease and illiteracy
are escalating? Chilisa (2005) suggested that ongoing research that fails to address the problem effectively
from the researched's frame of reference perpetuates conditions that violate human rights and impedes
progress toward social justice. Hence, pathways to strengthening the ethical character of research include
funding, conducting, disseminating, and using research based on philosophical positions that create space
for knowledge systems that recognize “local language and thought forms as an important source of making
meanings of what we research … Given the HIV/AIDS epidemic in Sub-Saharan Africa, the need for diversity
in research epistemologies has become not a luxury of nationalism of the African Renaissance, but rather an
issue of life and death” (p. 678).
The intransigence of social problems and the need to examine critically the philosophical assumptions that
undergird the ethics of research do not arise only in developing countries. Witness the difficulties in the United
States with regard to provision of educational, psychological, and social services to the poor and people with
disabilities or those who are from racial or ethnic minority groups. How is it that blacks in the United States are
more than four times as likely as whites to be diagnosed with schizophrenia? Blow et al. (2004) suggested
that diagnostic measures developed primarily with white patients in mind do not automatically apply to other
groups. How is it that males, especially those from minority ethnic and racial groups, are diagnosed as
having disabilities in much greater numbers by a ratio of about 2 males for every 1 female (U.S. Department
of Education, 2004)? Yet, at the same time, girls from all ethnic groups may be underidentified as having
certain disabilities because the indicators are manifested differently for females and for males. Therefore,
girls with undiagnosed disabilities are not receiving the supportive services necessary to succeed in school
and life (Mertens, Wilson, & Mounty, 2007), while minority children with disabilities all too often experience
inadequate services, low-quality curriculum and instruction, and unnecessary isolation from their nondisabled
peers (Losen & Orfield, 2002).
Another example of discrimination and oppression in the United States was made visible through the
differential aftermath of the devastation caused by Hurricane Katrina, which pounded the Gulf Coast states
in August 2005. Elliott and Pais (2006) conducted a survey of over 1,200 hurricane survivors to examine the
influence of race and socioeconomic class on evacuation timing, emotional support, housing, employment,
and plans to return to their pre-storm communities.
Results reveal strong racial and class differences, indicating that neither of those dimensions can
be reduced to the other when seeking to understand responses by survivors themselves. This
intersection renders low-income black home owners from New Orleans those most in need of
targeted assistance as residents work to put themselves and the region back together. (p. 295)
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This introductory commentary brings to the surface the need to examine critically the basic beliefs that
researchers bring with them to guide their decisions about what variables are important to consider and how
and from whom the data are to be collected in an ethical manner. In the context of educational, social, and
psychological programs, many of the people the programs are intended to serve are the ones who have
been pushed to the margins on the basis of race/ethnicity, language, indigenous/immigrant status, education
level, disability, age, religion, socioeconomic status, and other contextually dependent variables. Issues of
discrimination and oppression are commonly associated with those characteristics that are connected with
the focus of such programs and policies. For researchers who are aware of the historical and political factors
that surround program participants, the need to consider power issues associated with greater privilege in
society is apparent.
In this context, where intransigent social, educational, health, economic, civil, and environmental conditions
result in violations of human rights on a daily basis, the ethical conduct of research demands attention to a
full array of complexity. The use of a lens of transformation provides researchers with the means to address
explicitly issues of human rights and social justice. To that end, this chapter elucidates the transformative
paradigm with its accompanying philosophical assumptions as a way of examining the underlying beliefs that
define the role of the researcher as one of working in partnership for social change and challenging the status
quo.
The transformative paradigm (Mertens, 2005, 2007, 2009) is a framework of belief systems that directly
engages members of culturally diverse groups with a focus on increased social justice. Being firmly rooted
in a human rights agenda, the ethical implications of research are derived from the conscious inclusion of a
broad range of people who are generally excluded from the mainstream in society. Such research strives to
extend the meaning of traditional ethical concepts to reflect more directly ethical considerations in culturally
complex communities. Power issues in terms of determining research focus, planning, implementation, and
use are also examined from a transformative stance based on axiological assumptions related to respect for
communities that are pushed to the margins and recognition of the resilience that rests within community
members.
To be quite blunt, the usefulness of research as a means to social transformation is not a universally agreed
on concept. Gustavsen (2006) questioned the potential role of research for social transformation: “If we
really want to become involved in socially significant practical action with demands for long time horizons,
for relating to numerous actors and engaging in highly complex activities, perhaps the notion of linking such
involvement to research as traditionally conceived is futile” (p. 25). He concluded that an unsettling of the
status quo of research is needed; that is, research needs to be transformed to engage in a purer form of
democracy that will support the development of social relationships that embody a principle of equality for all
participants.
One of the major principles underlying transformative approaches to research is the belief in an often
overlooked strength in communities that are rising to the challenge of addressing seemingly intransigent
problems. When theoretical perspectives such as resilience theory, positive psychology, feminist theory, and
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critical race theory are used to frame a study, then a deliberate and conscious design can reveal the positive
aspects, resilience, and acts of resistance needed for social change. Ludema, Cooperrider, and Barrett (2001)
argued that research and evaluation have largely failed as instruments for advancing social-organizational
transformation because they maintain a problem-oriented view rather than focusing on the strengths of a
community. Historically, research and evaluation have had a deficit-based orientation, such that the “problem”
was derived from deficits found in the people whom the program was designed to help. They proposed turning
away from such a deficit-based view and looking instead at what is positive. The basis for social change is
seen as emanating from an unconditional positive question that reaffirms the life-giving and life-sustaining
aspects of organizational existence. Important exceptions to deficit-based programs and research provide
examples of resilience-based strategies, such as the Communities that Care System (Hawkins & Catalano,
2003; Chapter 22, this volume).
Transformative Paradigm
A paradigm is a set of metaphysical constructs associated with specific philosophical assumptions (basic
beliefs) that describe a person's worldview and serves to guide the organized study of that world (Denzin
& Lincoln, 2005). Bawden (2006) asserted that evaluators (and social researchers, by implication) have a
responsibility to critically examine their worldviews because they influence choices, either consciously or
unconsciously. He commented,
If indeed, as Stufflebeam (2001) argues, any evaluation is a study that is designed and conducted
to assist some audience to assess an object's merit and worth, then explicit attention must be paid
to foundational assumptions about the nature of worth and value, and to how these can come to be
known in any given contextual situation, if it is to be an ethically defensible practice. (p. 38)
There are four basic belief systems that are relevant to defining a paradigm in a research context, with
assumptions associated with each belief system:
1. Axiology: Assumption about the nature of ethical behavior
2. Ontology: Assumption about the nature of reality
3. Epistemology: Assumption about the nature of knowledge and who can know what by
what means
4. Methodology: Assumption about appropriate approaches to systematic inquiry
The axiological assumption asks, What is considered ethical or moral behavior? In transformative terms,
the question is asked, How can research contribute to social justice and the furtherance of human rights?
Ontologically speaking, how do we know what is real? In this chapter, this question is not asked about
physical objects, such as a desk in a room, but rather about a determination of the reality associated
with socially constructed concepts, such as literacy or health. The transformative ontological question asks,
Whose reality is privileged in this context, and what is the mechanism for challenging perceived realities
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that sustain an oppressive system? The epistemological question asks, What is the nature of knowing, and
what is the method for knowing the nature of reality and the means for generation of knowledge (Fonow &
Cook, 2005)? It brings up questions about who can know what and how the knower relates to what would be
known. If I am to genuinely know the reality of something, how do I need to relate to the people from whom
I am collecting data? The knower is the researcher, and the would-be-known is the participant in the study.
Should I be close to the participants so that I can really understand their experiences, or should I maintain a
distance between myself and the participants so that I can be “neutral”? This question raises concerns about
the definition of objectivity as it is operationalized in a research context. Methodologically, choices go beyond
quantitative, qualitative, or mixed methods to how to collect data about the reality of a concept in such a way
that one feels confident that one has indeed captured that reality and done so in an ethical manner.
Axiological Assumption
The transformative paradigm places priority on the axiological assumption as a guiding force for
conceptualizing subsequent beliefs and research decisions. Hence, this assumption is examined from a
number of different perspectives. A historical and contemporary view of social justice is defined in terms of
distributive justice. Theories of ethics are identified that are commensurate with the transformative paradigm.
Declarations of human rights provide insights into the meaning of social justice. Codes of ethics are
evolving in professional associations and from indigenous peoples that are compatible with the transformative
paradigm's axiological assumption. And the implications of regulatory concepts of ethics are examined from
the transformative perspective.
Distributive Justice
Aristotle's concept of social justice as distributive justice includes the idea that justice is achieved through
the equitable allocation and distribution of benefits (Reisch, 2002). In contrast to contemporary views of
distributive justice, Aristotle applied his principle of equity in terms of sharing resources only within the
hierarchical social stratum of the time, such that only men of property in Athens would come under the
distributive justice principle. Political and social revolutions in the late 18th century linked justice to equality
and human rights. However, continued oppression by the rich and powerful throughout history indicates that
the idealized notion of equality and human rights for all is not a reality.
Rawls (2001) raised the issue of the need to establish an imperative to act for the furtherance of social justice,
which was, up to that time, missing in others' discussions of the topic. He asserted in his maximin theory that
every person has an equal right to personal liberty and that social and economic equality demands that the
need of the least advantaged be given priority and the principle of equal opportunity be applied to all available
positions.
In contemporary writings about social justice, the attainment of social justice is linked with the goals of social
diversity and “with challenges to the normative power structure and the oppression it produces” (Hyde, 1998,
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cited in Reisch, 2002, p. 348). Reisch noted that a social justice approach may involve unequal distribution
of resources. However, unequal distribution of resources would be justified only if such inequalities served
to advance the least advantaged groups in the community (Franklin, 1998; Isbister, 2001). The pursuit of
social justice by researchers requires acknowledgment of the political dimensions of research contexts and
working cooperatively with community members to clarify goals. Although Reisch (2002) was writing about
social justice in the context of social work, his comments have applicability to understanding the meaning of
social justice in a transformative research context as well:
A social justice perspective also contains the imperative of challenging prevailing assumptions about
power, privilege, and various forms of oppression in the theories that underlie current policies,
programs and methods. … This requires us to advocate for the elimination of those policies that
diminish people's sense of control over their lives… Simultaneously, we need to work for the
expansion of those programs that enable people to exercise personal freedom by… making them
feel like integral and valued parts of society. These goals reflect a potential synthesis of the historic
division between individual and collective well-being at the heart of debates over social justice and
may provide the basis for its attainment in an increasingly diverse and conflict-ridden world. (p. 351)
Theories of Ethics
Simons (2006) identified rights-based and social justice theories of ethics that are commensurate with the
transformative axiological assumptions. Rights-based theories justify their actions on the basis that every
person must be treated with dignity and respect and that the avoidance of harm must be the primary principle.
The social justice theory of ethics takes the rights-based theory to a group or societal level (House, 1993),
leading to an awareness of the need to redress inequalities by giving precedence, or at least equal weight, to
the voices of the least advantaged groups in society. The implicit goals of inclusion of those who have been
denied access to power are an accurate representation of their viewpoints, as well as support for the less
advantaged in terms of their being able to take the role of an active agent in social change.
Human Rights Declarations
The transformative paradigm is firmly rooted in a human rights agenda much as it is articulated in the United
Nations (UN) Universal Declaration of Human Rights (1948). Although the declarations of the UN are situated
in a multilateral context, they provide guidance in understanding a basis for transformative work nationally as
well as internationally. Human rights is a globally relevant issue; “developed” countries are not exempt from
violations of human rights.
The UN's declaration is based on the recognition of the inherent dignity and of the equal and inalienable
rights of all members of the human family, including the rights to life, liberty, security of the person, equal
protection under the law, freedom of movement, marriage with the free and full consent of the intending
spouses, ownership of property, freedom of thought and religion, freedom of opinion and expression,
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peaceful assembly, participation in governance, work in just and favorable working conditions, and education.
Importantly for this text, Article 25 reads,
Everyone has the right to a standard of living adequate for the health and well-being of himself
[sic] and of his [sic] family, including food, clothing, housing and medical care and necessary social
services, and the right to security in the event of unemployment, sickness, disability, widowhood, old
age or other lack of livelihood in circumstances beyond his [sic] control. (UN, 1998)
The UN Universal Declaration contains language indicating that everyone is entitled to these rights, without
distinction of any kind, such as race, color, sex, language, religion, political or other opinion, national or social
origin, property, birth, or other status. However, the UN recognized that the Universal Declaration did not
result in enjoyment of the rights contained therein for all people. They noted that specific attention would need
to be given to groups that were not being afforded these rights based on race, disability, gender, age, political
standing, or status in the workforce. Consequently, they approved the following:
• The International Convention on the Elimination of All Forms of Racial Discrimination in 1969, which
affirms the necessity of eliminating racial discrimination throughout the world in all its forms and
manifestations and of securing understanding of and respect for the dignity of the human person.
• The Declaration on the Rights of Disabled Persons (UN, 1975), which assures them the same
fundamental rights as their fellow citizens, no matter what the origin, nature, and seriousness of their
handicaps and disabilities. The UN subsequently developed and approved the Convention on the
Rights of Persons With Disabilities in December 2006 (UN, 2006a).
• The Convention on the Elimination of All Forms of Discrimination Against Women (UN, 1979), which
provides the basis for realizing equality between women and men through ensuring women's equal
access to, and equal opportunities in, political and public life—including the right to vote and to stand
for election—as well as education, health, and employment.
These were followed by the Convention on the Rights of the Child (UN, 1990a) and the International
Convention on the Protection of the Rights of All Migrant Workers and Members of Their Families (UN,
1990b). After 20 years of debate, the UN finally approved the Declaration of the Rights of Indigenous
Peoples (UN, 2006b). Subsequently, the UNICEF, with the endorsement of the International Organization
for Cooperation in Evaluation and the International Development Evaluation Association, prepared a report
based on a meeting of 85 evaluation organizations that maps the future priorities for evaluation in that context.
This excerpt captures the emphasis on human rights:
Within a human rights approach, evaluation should focus on the most vulnerable populations to
determine whether public policies are designed to ensure that all people enjoy their rights as citizens,
whether disparities are eliminated and equity enhanced, and whether democratic approaches
have been adopted that include everyone in decision-making processes that affect their interests.
(Segone, 2006, p. 12)
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Professional and Indigenous Codes of Ethics
In addition to guidance on human rights issues from international bodies, codes of ethics from relevant
professional associations and organizations provide guidance for researchers and evaluators as to what
constitutes ethical practice (see Chapter 7, this volume). These codes of ethics have been critically reviewed
and revised to reflect a greater concern for principles that are reflective of the axiological assumptions of
the transformative paradigm. The American Evaluation Association (AEA) modified its guiding principles to
include an explicit principle related to the role of cultural competency in ethical evaluation practice. The
American Psychological Association (APA) revised its ethics code in 2002, strengthening protection of people
in research that involves deception (Fisher, 2003). Ethics in psychology has also been extended by Brabeck's
(2000) application of feminist principles in psychology (see also Chapter 3, by Brabeck & Brabeck, this
volume).
Two subgroups of the APA1 also developed multicultural ethical guidelines for research. The implications for
research methods derived from the guidelines that are most relevant to the transformative paradigm read as
follows:
Related to the research question is choosing culturally appropriate theories and models on which
to inform theory-driven inquiry … Psychological researchers are encouraged to be aware of and,
if appropriate, to apply indigenous theories when conceptualizing research studies. They are
encouraged to include members of cultural communities when conceptualizing research, with
particular concern for the benefits of the research to the community. (APA, 2002, p. 3).
The Guidelines for Research in Ethnic Minority Communities contains the following description of the
researcher's ethical responsibilities:
As an agent of prosocial change, the culturally competent psychologist carries the responsibility
of combating the damaging effects of racism, prejudice, bias, and oppression in all their forms,
including all of the methods we use to understand the populations we serve … A consistent theme …
relates to the interpretation and dissemination of research findings that are meaningful and relevant
to each of the four populations2 and that reflect an inherent understanding of the racial, cultural, and
sociopolitical context within which they exist. (APA, 2000, p. 1)
Interestingly, the APA endorses the role of the psychologist as an agent of prosocial change; this is reflective
of the axiological assumption of the transformative paradigm that ethical research is defined by its furtherance
of social justice and human rights, all the while being cognizant of those characteristics associated with
diverse populations that impede progress on these fronts.
Researcher guidelines are also available from indigenous communities that provide insights into the ethical
grounding of research (see Cram, 2001; Chapter 20, this volume). Researchers from the Sign Language
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community3 adapted the Mãori Terms of Reference to their own specific context (Harris & Holmes, 2007;
Harris, Holmes, & Mertens, in press). The complexity of the Deaf4 community as a cultural and linguistic
minority includes dimensions such as levels and type of hearing loss, parental hearing status, access to
and ability to benefit from auditory enhancing technologies, language usage based on signs and/or voice,
and use of visually accessible sign languages. Their ethical guidelines, Sign Language Communities Terms
of Reference, are commensurate with the transformative paradigm. Representative guidelines of particular
significance to Sign Language communities include the following:
• Research involving the Sign Language community has to be done “by Deaf, for Deaf and with Deaf.”
• Instead of using spoken language and providing interpreters for Deaf members, research projects
should mandate sign language as the primary language of research teams, interpreters should be
provided for hearing people who do not know sign language, and bilingual publications in sign
language and the majority language should be accepted and encouraged.
• There should be increased emphasis on confidentiality because of the compactness of the Sign
Language community and because the visual nature of sign language requires documentation
through video (as opposed to audiotapes or transcribed interviews), making it difficult to preserve
anonymity.
Regulatory Concepts of Ethics
The transformative paradigm pushes the regulatory principles of respect, beneficence, and justice on several
fronts. Respect is critically examined in terms of the cultural norms of interaction in diverse communities
and across cultural groups. Consent is obtained with full awareness through appropriate culturally competent
means. It includes self-awareness in relationship to community. (See Chapter 26, this volume, in which the
author, Chilisa, explains the African ethical principle of umbuntu; Chilisa & Preece, 2005.) Beneficence is
defined in terms of the promotion of human rights and increase in social justice. An explicit connection is
made between the process and outcomes of research and furtherance of a social justice agenda.
Commensurate Theories
The theoretical and axiological thinking of critical theorists, feminists, and other human rights advocates has
much to offer in the consideration of ethical principles in research. The ethical principles underlying feminist,
critical, postcolonial, and indigenous theories are commensurate with the axiological assumptions of the
transformative paradigm (see Chapters 4, 9, 20, and 26, this volume).
Ontological Assumption
The ontological assumption of the transformative paradigm holds that reality is socially constructed; however,
it does so with a conscious awareness that certain individuals occupy a position of greater power and that
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individuals with other characteristics may be associated with a higher likelihood of exclusion from decisions
about the definition of the research problem, questions, and other methodological aspects of the inquiry.
Ontological assumptions rooted in positivist philosophy have been criticized by many groups who have been
pushed to the margins in the scholarly decolonization literature. A critique from Native American communities
notes that
production of meaning from a Eurocentric perspective does not capture any “truth” of Native and
tribal lives but also infiltrates Native lifeworlds in the form of “epistemic violence.” (Spivak, 1988, p.
126, as cited in Duran & Duran, 2000, p. 96)
Social scientists have been rewriting tribal canonical texts (i.e., ritual) via anthropology and other
disciplines since first contact and therein have produced meaning that has changed and distorted
tribal understandings or forced them underground. Clinical psychology as well as research-oriented
psychology is extremely narrow-minded. The assumptions of these fields are based on a utilitarian
worldview. … Western empirical research is based on the illusion of objectivity, with a transhistorical,
transcultural orientation. It operates within an a priori essentialist Cartesian model of a unified,
rational, autonomous subject, the construction of which is problematized in the work of French
poststructuralism and German critical theory. (Duran & Duran, 2000, p. 96)
The ontological assumption asks the question, What is real? In a research context, researchers identify
variables and measure aspects of those variables in an attempt to look for objective truth, what is real within
some level of defined probability, or truth as defined within a complex cultural context. A transformative lens
focuses the ontological question on an explicit acknowledgement that reality is socially constructed and that
specific characteristics associated with more or less power determine which version of reality is accepted as
“real.” Power issues pervade the choice of variables and their definitions, determining what is “researchable.”
Power is implicit in decisions about which interpretation of reality is accepted. This point is illustrated in the
power associated with explanations of the achievement gap between minority and majority students (e.g.,
based on either race or hearing status) in the United States.
O'Connor and Fernandez (2006) described the results of a National Research Council (NRC) report that
explored the assumptions associated with the relationship between poverty and the overrepresentation of
minority youth in special education. They provided a critique indicating that this explanation oversimplifies
the concept of compromised development associated with being poor and underanalyzes the effect of culture
and the organization of schools that situate minority youth as academically and behaviorally deficit, thus
increasing the probability that they will be placed in special education. They noted that the NRC recognizes
that children in high-poverty districts are exposed to a higher degree of teacher bias and have lower funding,
which is necessary to reduce class size and attract qualified teachers. However, the NRC concludes that
these variables contribute to the incidence of disability. O'Connell and Fernandez described a different reality
based on the evidence:
It is schools and not poverty that place minority students at heightened risk for special education
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placement. … [T]here is nothing about poverty in and of itself that places poor children at academic
risk; it is a matter of how structures of opportunity and constraint come to bear on the educational
chances of the poor to either expand or constrain their likelihood of achieving competitive,
educational outcomes (O'Connor, 2002). Disproportionality, then, is the structured probability with
which minority youth are more likely to be “documented” as disabled. (p. 10)
People who wrote the legislation in the United States about education for people with disabilities based
national policy on a reality that assumes that D/deaf/hard-of-hearing students placed in mainstream settings
are more successful at academics than those placed in a residential environment. Administrators and local
school district board members encourage parents of D/deaf/hard-of-hearing children to place their children
in mainstream settings under the assumption that these represent the least restrictive environment for them
(Individuals With Disabilities Education Improvement Act, reauthorized 2004). However, Deaf and hard-of-
hearing students in residential schools achieve as much as or more than those in mainstream environments
(Marschark, Lang, & Albertini, 2002). The social abilities of Deaf and hard-of-hearing students in residential
schools are higher than those of students at public schools because they have Deaf role models, full access
to direct communication, and peer interaction. Nevertheless, most D/deaf students in mainstream settings are
placed in self-contained classrooms with minimal social interaction with hearing peers and often little to no
interaction with other deaf students. Some of them work 1:1 with a special education teacher who may not
know anything about Deaf culture, sign language, or teaching D/deaf children.
Ladson-Billings (2006) made a similar argument in her explanation of the “achievement gap” when minority
and disadvantaged students are compared with their white and privileged counterparts. She explained that
a significant amount of research on poor, African American, Latina/o, American Indian, and Asian immigrant
students has led to very few solutions. A long history of educational research gives privilege to the explanation
that race/ethnicity and/or poverty is to blame for the lack of academic achievement. Should researchers
explore the historic, economic, sociopolitical, and moral debt in the United States that results in poor
opportunities for quality educational experiences for those pushed to the margins? What is required is a
serious investigation of the costs of segregation and the costs of equitable funding and to use research and
evaluation to understand that “a cumulative effect of poor education, poor housing, poor health care and poor
government services create a bifurcated society that leaves more than its children behind” (Ladson-Billings,
2006, p. 10).
Epistemological Assumption
The epistemology of the transformative research paradigm queries the nature of knowledge and who can
know what about whom, leading to questions about the nature of the relationship between researcher and
participant. Transformative epistemology is characterized by a close collaboration between researchers and
participants of a study, whether they are community leaders or members of organizations. Communication is
achieved by the use of participants' language of choice. The research purpose, design, implementation, and
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utilization are developed and implemented with appropriate cultural sensitivity and awareness. Researchers
require collaboration with the host(s) of the community, not necessarily the leaders but people of the
community. The relationship is interactive and empowering. It requires that trust be built through observance
of appropriate cultural norms.
The epistemology of the postpositivist stance is reflected in the early work of Campbell, in which he
envisioned an experimenting society that would lead to incremental reform as knowledge was gained through
random assignment to alternative treatments (Campbell & Stanley, 1966). This approach included the notion
that researchers should be value neutral to produce scientifically valid knowledge. Christians (2005) criticized
this postpositivist notion that “a morally neutral, objective observer will get the facts right” (p. 148). He
asserted that ethical behavior must be cognizant of the “power relations associated with gender, sexual
orientation, class, ethnicity, race, and nationality” (p. 148).
The inherent danger of paradigms and the prevailing hegemonic discourse in the academic field prevents
us from realizing that there are multiple truths. Not only that, false information can easily be perpetuated by
those in power. For instance, in Psychology of Deafness, Myklebust (1964) claimed that D/deaf people were
more immature; had increased emotional problems; were more naive and primitive; were inferior in physical
coordination; exhibited marked retardation in language; were only able to complete concrete tasks; and
were schizophrenic, maladjusted, belligerent, subhuman, isolated, paranoid, neurotic, suspicious, psychotic,
dependent, and depressed. He also claimed that D/deaf males were effeminate and D/deaf females were
masculine. At that time, Myklebust was a hearing researcher who did not meaningfully involve D/deaf people
in his research. The majority of the research in the Deaf community is done by hearing people (Lane, 1999).
Academic power is achieved through controlling academic discourse and by devaluing the discourses of the
underrepresented, such as D/deaf people. Research in the field of D/deaf education typically focuses on the
abilities D/deaf people lack rather than the abilities D/deaf people have. That in itself is oppressive (Erting,
1992; Evans, 2004; Lane, 1999). A “D/deaf-as-deficient” focus is a way for people in power to keep control of
academic knowledge and maintain their positions of power.
What do we gain or lose in our struggle for ethical behavior by allowing the perspectives of feminists, critical
theorists, postcolonialists, and others who are steeped in multivocal and cross-cultural representation to raise
questions and proffer different bases of what is accepted as real in the ethical domain? What do we gain by
having these conversations at the borders and intersections of ethics in research and evaluation?
In the transformative paradigm, the issues of understanding culture and building trust are paramount. There
are complications associated with this assumption. For example, suppose a researcher is studying people
who do violence to gays or lesbians or studying a white supremacist group. What does it mean to understand
culture and build trust in such a context? This is one of the many tensions that surfaces in transformative
work. A partial answer comes from an understanding of the notion of privilege and the interrogation of
unearned privilege. Kendall (2006) explained,
The superiority of whiteness is a social construct, created by some white men but in all our names.
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This construct informs both the past and the present and affects each of our lives daily. All of us
who are white receive white privileges. … We can use them in such a way as to dismantle the
systems that keep the superiority of whiteness in place. One of the primary privileges is having
greater influence, power, and resources. … As white people, we keep ourselves central, thereby
silencing others. … If we look at race in North America as only a Black-white construct, we miss the
true purpose of the system. We must be aware of how the power holders oppressed all people of
color to shape the country as they wanted it. Racism is one of several systems of oppression. Others
are class, sexism, heterosexism, the institutionalized primacy of Christianity, and able-bodiedism.
These systems work toward a common goal: to maintain power and control in the hands of the
wealthy, white, heterosexual, Christian, able-bodied men. Examining the intersections is essential to
understanding the intentional and finely crafted nature of the system. Finally, this system is brilliant
but not impervious to change. We can dismantle it if we know it well and work together toward that
goal.
Researching from a transformative stance necessitates working from a multiplicity of vantage points. Kendall
(2006) reminded us that studying “whiteness” as a metaphor for power that oppresses is a necessary
part of understanding discrimination and oppression, thereby making visible the tensions associated with
relationships between researchers and communities, especially when the research focuses on oppressive
societal systems.
Building trust and relationships while engaging in critical self-reflection expands thinking around the traditional
concept of objectivity in research. As a challenge to the “status quo” of research, Heron and Reason (2001)
asked questions such as
Isn't it true that people can fool themselves about their experience? Isn't this why we have
professional researchers who can be detached and objective? The answer to this is that certainly
people can and do fool themselves, but we find that they can also develop their attention so
they can look at themselves—their way of being, their intuitions and imaginings, their beliefs and
actions—critically and in this way improve the quality of their claims of knowing. We call this “critical
subjectivity;” it means that we don't have to throw away our personal, living knowledge in the search
for objectivity, but are able to build on it and develop it. We can cultivate a high-quality and valid
individual perspective on what there is, in collaboration with others who are doing the same. (p. 149)
Epistemology and Indigenous Peoples
Gordon (1990) wrote about the need for African American epistemology in educational theory and practice.
Wright (2003) supported the notion of understanding epistemology within the context of the African American
experience when he cited the work of Scheurich and Young (1997, 1998) on “coloring epistemologies,”
Delgado Bernal (1998) on Chicana feminist epistemology, Ladson-Billings (2000) on an “ethnic epistemology,”
and Dillard (2000a, 2000b) on an “endarkened feminist epistemology” (p. 198).
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Dillard's (2000a, 2000b) endarkened feminist epistemology is based on the intersection of race, gender,
nationalism, and spirituality. She used a sociocultural identity rather than a biological conception of race and
gender. She explicitly acknowledged research as a political and utilitarian tool associated with an obligation
to the black community and as an intervention to disrupt the white, hegemonic research paradigm. She
spoke of “research as a responsibility answerable and obligated to the very persons and communities being
engaged in the inquiry” (Dillard, 2000b, p. 663). She called for a “transformation at the epistemological level
if education research is to truly change or transform” (Dillard, 2000b, p. 663). The concept of endarkened
feminist epistemology brings with it a change in the role of the researcher to that of a supportive and reflective
activist in the community, as well as one who challenges the prevailing research establishment.
Audism and the Deaf Experience
When, where, and how did the paradigm of D/deaf people as deficient emerge? This paradigm can be
traced back many centuries when the definition of language was directly associated with speech and civilized
behavior and any other forms of communication were considered savage and restricted to animals. The
historical analysis of this deficit paradigm is an important topic discussed in detail by other researchers
(Bauman, 2004; Branson & Miller, 2002). In research ethics with the Deaf community, this deficit paradigm
takes the form of audism. Audism is a term that was originally coined and defined by Humphries (1977) as
“the notion that one is superior based on one's ability to hear or behave in the manner of one who hears” (p.
12). Humphries continued by explaining that not only is audism perpetuated by hearing people toward D/deaf
people, but it also occurs between D/deaf people, where, for instance, a D/deaf person oppresses another D/
deaf person by expecting the same behavior expected from hearing people.
Methodological Assumptions
Methodological assumptions involve the philosophical basis for making decisions about appropriate methods
of systematic inquiry. Inclusion of a qualitative dimension is critical in transformative research as a point
of establishing a dialogue between researchers and community members. Mixed-methods designs can be
considered in order to address the information needs of the community. However, methodological decisions
are made with a conscious awareness of contextual and historic factors, especially as they relate to
discrimination and oppression. Thus, the formation of partnerships between researchers and the community
is an important step in addressing methodological questions in research (see Chapter 22, this volume).
Research in the transformative paradigm is a site of multiple interpretive practices. It does not have a specific
set of methods or practices of its own. This type of research draws on multiple strategies, methods, and
techniques emanating from different theories and approaches. The methodological assumptions associated
with the transformative paradigm are commensurate with approaches such as participatory research, action
research, and feminist research and, as such, provide a philosophical framework to integrate research and
evaluation for social transformation. Richardson and St. Pierre (2005) used the concept of crystallization as a
guiding principle because of the inclusion of different perspectives, such as fiction, field notes, and scientific
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articles. Researchers get more out of their research study by listening and valuing each member's “voice”
through crystallization, not limited to three sides, as in triangulation, but maximized through several possible
approaches. There is not one “correct” way of approaching the study but several different points of view.
Transformative ethical considerations need to occur at multiple points in the research process, from
discussions of basic beliefs and paradigmatic stances to the establishment of the focus of the research and in
all subsequent decisions regarding methods; sampling; and data collection, analysis, and use. For example,
sampling needs to be reframed to reveal the dangers of the myth of homogeneity, to understand which
dimensions of diversity are important in a specific context, to avoid additional damage to populations by using
labels such as “at risk” that can be demeaning and self-defeating, and to recognize the barriers that exist to
being part of a group that can contribute to the research results. The transformative paradigm also leads us
to reframe data collection decisions to be more inclined to use mixed methods, while at the same time being
consciously aware of the benefits of involving community members in data collection decisions, assessing
the appropriateness of methods with a depth of understanding of the cultural issues involved, building trust to
obtain valid data, designing modifications that may be necessary to collect valid data from various groups, and
linking data collection to social action. Methodological questions with ethical implications include the following:
• What are the important dimensions of diversity to include in research in order to give accurate and
appropriate representation to groups that have been pushed to the margins of those with more
privilege in society?
• What is the ethical responsibility of the researcher to identify and appropriately address those
dimensions of diversity?
• What is the ethical cost of ignoring or inappropriately representing the dimensions of diversity in
research?
Methodological issues for working within a framework that promotes social justice, dimensions of diversity,
and cultural competency are discussed further in many chapters in the methodological section of this
Handbook.
Conclusions: Social Action
The authors raise questions that require continued discourse with members of oppressed groups. Several
questions need to be addressed in transformative research—for instance, What are the challenges
associated with establishing an ethical relationship in research, and what are the ethical strategies for
determining ownership of the research data and results? The researcher, participants, and community
members need to discuss who has the power and how the balance of power can be shifted to support those
with less power.
The transformative paradigm emphasizes the need for trust between researcher and participants; many
challenges arise in developing a trusting relationship. Researchers need to examine critically the risks and
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roles for themselves when conducting research in culturally complex communities, especially when they are
in direct engagement with members of culturally diverse groups with a focus on increased social justice.
Helpful insights come from critiques in scholarly literature from Africa (Chilisa, 2005) and New Zealand (Smith,
2005).
Language and communication are also considered as challenges when research is conducted with
communities that do not use the dominant language. If the dominant language is the language of the
oppressor, then researchers and participants need to establish which language(s) is (are) used in research
team meetings, in the field, in e-mail correspondence, in field notes, and in personal journals. This should be
discussed explicitly among the research team members and participants. The team needs to agree on when
it is okay to use the majority language and when is it not. Earlier in this chapter, when the issue of language
was raised, it was asserted that the language used should be the one selected by the participants. Of course,
in many studies, not all participants use the same language—another challenge.
Another challenge that transformative researchers might experience is the publication and dissemination of
findings. Academic power and knowledge are critical to publish scholarly work successfully. Gilmore and
Smith (2005) argued that the academic genre not only involves knowing the rules of academic writing but also
includes insider knowledge about creating and disseminating that knowledge. To exercise academic power,
one must know how to write according to the paradigm of the field—in other words, one must be cognizant
of the beliefs of the people involved in controlling the knowledge of the field. However, strict adherence
to the limits of disseminating research knowledge through the lens of academia blinds us to “alternative
explanations or perceptions of the same phenomena” (Grushkin, 1998, p. 182). This blindness promotes
hegemonic control of what information may or may not enter the field. Transformative researchers are not
exempt from this need for critical self-reflection.
For instance, until recently, academic journals in the social sciences frowned on citing “experience” and
continue to show explicit preference for citing “research literature” (Gilmore & Smith, 2005). Gilmore and
Smith argued for indigenous voices, saying that the experience of other community members should be
valued, by placing the underrepresented's voices on an equal footing with citations of research literature.
For example, in the case of the Deaf community, primacy should be given to Deaf people's experience and
perspective. This may necessitate that publications be bilingual (in print English and video-based sign) and
made accessible to community members first before the rest of the world. After all, it is their information to
begin with, and it is about them as a community.
In conclusion, researchers and participants working together in a collaborative manner need to address
challenges throughout the research process. We need to consider the challenge of respecting the ownership
of knowledge by a community, then publishing and disseminating for the majority language and culture. One
might, therefore, ask, Why does the world know about research first in a language that is not the community's
language? Why make the language of the oppressor superior? From a transformative stance, researchers
working with community members and coresearchers operate with a conscious awareness of the nature
of challenges to ownership, power, and communication among outsiders and insiders of the researched
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community. A quote from bell hooks (1993), a critic of white supremacist capitalist patriarchy, illustrates the
transformative point of view: “If we want a beloved community, we must stand for justice, have recognition for
difference, without attaching difference to privilege” (p. 10).
The transformative researcher feels a moral imperative to challenge the status quo for the purpose of
contributing to a more just society.
Notes
1. The Council of National Psychological Associations for the Advancement of Ethnic Minority Interests
(CNPAAEMI) is made up of the presidents of the five national ethnic/racial minority professional associations,
Asian American Psychological Association, Association of Black Psychologists, National Hispanic
Psychological Association, Society for the Psychological Study of Ethnic Minority Issues (Division 45 of
APA), and Society of Indian Psychologists, and the president (or his or her designee) of the APA (2002).
The CNPAAEMI published Guidelines for Research in Ethnic Minority Communities (APA, 2000), and the
APA's Joint Task Force of Division 17 (Counseling Psychology) and Division 45 (Psychological Study of
Ethnic Minority Issues) published Guidelines on Multicultural Education, Training, Research, Practice, and
Organizational Change for Psychologists (APA, 2002).
2. The APA developed guidelines for four specific groups: Asian American/Pacific Islander populations,
persons of African descent, Hispanics, and American Indians.
3. Sign Language communities refer to people whose primary experience and allegiance is with Sign
Language as a cultural component of the Deaf community and culture. However, all researchers who conduct
research in Sign Language communities should be conscious about the complexity of deaf people and the
Sign Language community. The capitalization of the term, Sign Language signifies a cultural group, similar to
African Americans and the Jewish community.
4. The American Heritage Dictionary of the English Language, Third Edition, (1992) defines Deaf as “of
relating to the Deaf or their culture” and deaf as the “lack of hearing sense.” Ladd (2003) elaborated on
the lowercase deaf terminology, which refers to people who wish to retain their membership and primary
experience with the cultural majority. The authors try their best to keep the distinction clear throughout the
paper.
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- Transformative Research and Ethics
- In: The Handbook of Social Research Ethics