Towards a Critical
Health Psychology Practice
Isaac Prilleltensky
Ora Prilleltensky
Peabody College,
Vanderbilt University
In Press: Journal
of Health Psychology
Correspondence should be sent to Isaac Prilleltensky, Department
of Human and Organizationla Development, Peabody College, Box 90, Vanderbilt
University, Nashville, TN, 37203, USA. Electronic correspondence may be sent to
Isaac.Prilleltensky@vanderbilt.edu
Abstract
The field of critical psychology is exerting an
influence in the way various sub-disciplines within psychology operate. In this
article we use a critical psychology framework to review the field of health
psychology. Through the use of values, assumptions, and practices we review progress
in health psychology and offer recommendations for aligning contemporary
practices with current thinking in critical psychology. We discuss typical
expectations, critical formulations and critical practice for interventions
with individuals, groups and communities along these dimensions.
Introduction
The purpose of this article is
to offer critical perspectives on the promotion of health and wellness. Within
the field of psychology, health psychology has been the champion of health promotion
and maintenance. In recent years, critical perspectives with respect to health
and wellness have made inroads into the social sciences (see Murray & Chamberlain, 1999; Stainton- Rogers,
1966; and special issue of Journal of Health Psychology on Reconstructing
health psychology, 2000, volume 5, issue 3). Critical psychology frames
health and wellness in ways that differ from mainstream health psychology
(Crossley, 2001a). In this article we conceptualize health and wellness from a
critical psychology perspective and formulate recommendations for interventions
with individuals, groups, and entire communities. By so doing, we wish to add
to the growing body of literature on critical health psychology. This
literature critiques and interrupts mainstream discourses that fail to address
issues of power, privilege and the social embeddedness of health and illness
(Marks, 2002).
Health is central to wellness.
It is a precursor as well as a consequence of wellness. We conceptualize wellness
in broad terms that include psychological and physical health. Wellness is a
satisfactory state of affairs, brought about by the combined presence of
values, resources, programs and policies (Prilleltensky, Nelson, & Peirson,
2001a, b). Each one of these four components contributes to health. We regard
health as an intrinsic as well as an extrinsic value. It has merit on its own
accord, but it is also instrumental in bringing about self-determination,
personal growth, and opportunities in life.
The way the World Health
Organisation (WHO) defines health is reminiscent of our notion of wellness.
According to the WHO, health is more than the absence of illness, it comprises
positive physical and emotional features that enable individuals and groups to
pursue their goals in a context of equality and justice (Tones, 1996). We
resonate with this inclusive definition, as it encompasses values of
self-determination, caring and compassion, personal growth, democracy, equality
and justice.
Health can be promoted,
maintained, and restored in micro (e.g., close personal relations, family),
meso (e.g., school, work), and macro spheres (e.g., community, society). From a
critical psychology perspective, each one of these contexts is suffused with power
differentials that privilege the powerful and discriminate against the weak
(Kawachi, Kennedy, & Wilkinson, 1999; Kim,
Millen, Irwin, & Gersham, 2000; McCubbin, 2001; Petersen, 1994; Prilleltensky
& Nelson, in press). Freund and McGuire (1999) claim that power is a strong
determinant of health. In their view, there is a strong connection between the
two, illustrated by
the power of workers over
their work pace; the power of people to control the quality of their physical
environments; the power of various groups or societies to shape health policy
or to deliver what they consider healing; the power of people of different
statuses to control, receive, and understand information vital to their
well-being; and the power of the mass media to shape ideas about food and
fitness (Freund & McGuire, 1999, p. 7).
Power is cardinal to the entire enterprise of
critical psychology. It is instrumental in the promotion of wellness, in
resisting oppression and in striving for liberation (Prilleltensky & Nelson,
2002). A recent special issue titled Power, Control, and Health (Journal of
Community & Applied Social Psychology, McCubbin, 2001), further elucidates
the inextricable relationship between health and power.
|
Insert
Table 1 about here |
Table 1 provides a synopsis of
how critical psychology values, assumptions and practices may guide the process
as well as the content of critical health work (Fox & Prilleltensky, 1997).
As a case in point, we note how the value of self-determination needs to
be contextualized in light of disability and chronic illness. The much-esteemed
value of autonomy needs to be rethought, and replaced, by the value of
interdependence. The value of diversity reminds us that there are many ways of
being, and living with a disability should not detract from a respected and
dignified life. When we value physical independence above all else and
regard it as imperative to a positive sense of self, we marginalize and exclude
those who cannot attain it. Critically reflecting on the values and assumptions
that support our work will benefit our research, teaching, and clinical
practice.
Power=s
omnipresent character is highlighted in table 1. Power differentials across the
medical divide have to be carefully attended to by critical health
psychologists. Chamberlain (2000) notes the lack of attention paid to critical
perspectives in health psychology. Similar sentiments are expressed by Stam
(2000): "In a related sense, it is strange, if not suspicious, that
discussions of the deeply contested, political and social issues that make up
health care today are absent from health psychology" (p. 276). Our own
potential to abuse power in a setting that accentuates the privilege of
professionals must be monitored (Prilleltensky, 1999).
Advocacy is a key feature in
health settings. Patients have to negotiate their treatment with professionals
who are not always sensitive to the psychological condition of the person
seeking help. One of us has worked in a rehabilitation hospital with patients
who had sustained various orthopaedic and neurological disorders. In one
particularly memorable case, a patient had to negotiate with one of his
treating therapists that it is pointless to spend his therapy time on making
himself a cup of tea. He had never done this for himself prior to the stroke,
and would certainly not begin to do so now - when it was extremely
time-consuming and onerous. The fact that he had to make a special case and
gain support from his psychologist, speaks volumes about the risk of
professional appropriation of decision-making. But advocacy should
extend beyond the walls of the clinic or the hospital. In our discussion of
roles for critical psychologists we distinguish between individual, group,
community, and societal interventions (Winett, 1995).
Tasks and Expectations
The term Health Psychology first appeared in the
professional literature in the late 1970s (Marks, 2002). Whilst the initial
focus was on treatment compliance and on the client-professional relationship,
it has grown and evolved into a diverse field that has gained much
recognition within psychology and allied health professions in the last 25
years. It is a growing field with a few journals, international conferences,
divisions or committees in the major psychological associations, and extensive
literature. Taylor offers a useful definition of the field of health
psychology. According to her
Health psychology is the field within psychology
devoted to understanding psychological influences on how people stay healthy,
why they become ill, and how they respond when they do get ill. Health
psychologists both study such issues and promote interventions to help people
stay well or get over illness. (Taylor, 1995, p. 3)
This
broad-based definition reflects the dual focus on research and practice that
characterizes the field of Health psychology.
As noted earlier, critical perspectives within Health
Psychology have gathered momentum in the past few years. Marks (2002)
conceptualizes critical health psychology as one of four alternative approaches
evolving within the field, alongside clinical health psychology, public health
psychology, and community health psychology. Whereas the other approaches focus
on patients in the health care system (clinical health psychology), schools and
work sites (public health psychology) and entire communities (community health
psychology), "Critical Health Psychology aims to analyse how power,
economics and macrosocial processes influence and/or structure health, health
care, health psychology, and society at large" (Marks, 2002, p.15). Although
critical health psychology brings to sharp relief the role of culture and
dominant societal structures, its power analysis may be applied from the micro
setting of relationships to the macro level of policy.
The importance of deconstructing the assumptions that
underline research in health psychology have been noted by Chamberline (2000)
and Stam (2000), amongst others (Crossley, 2000). Stam (2000) questions mainstream
health psychology's noncritical and nonreflexive definition of health and
illness. So long as we define health as simply regaining the ability to
perform, and adopt a likewise uncritical stance towards such constructs as
'adjustment' and 'quality of life', "we deny that we are collectively, as
a profession, defining a set of outcomes for others@ (p. 279). Only by negotiating the meaning of such
constructs with affected individuals, can we hope to create research and
practice that is relevant, effective, and empowering.
Writing about the proliferation of qualitative
research projects in health psychology, Chamberlin (2000) warns that an
increased emphasis on methodology issues often comes at the expense of
critically reflecting on the assumptions which support the research. Like their
quantitative counterparts, most qualitative studies in health psychology fail
to adopt a critical perspective and ignore the philosophical positions of the
researcher. In a similar vein, Wilkinson (2000) demonstrates how different
feminist research traditions (positive empiricist, experiential, and
discursive) can be effectively applied to breast cancer research that is
informed by a critical perspective.
Although we acknowledge the growing importance of
critical health psychology research, the rest of this paper will be devoted to
health psychology practice. Health and medical settings continue to be
the largest employers of psychologists in recent years (Stam, 2000). The
services offered by health psychologists include coping with physical illness,
pain management, psychosocial rehabilitation after accidents, promotion of
healthier lifestyles, support groups for sufferers of chronic disease, and the
like. These activities fall into two broad categories: clinical services in
medical settings (Belar & Deardorff, 1995; Bennett, 2000), and health
promotion programs in community settings (Bennett & Murphy, 1997). Taking
into account these two major domains, table 2 describes potential interventions
for critical health psychologists. The interventions vary along timing,
population, and ecological levels. Across the top of the table we can see
different units of interventions: individuals, groups and organisations, and
community and society. Each unit of intervention is guided, respectively, by a
set of personal, relational, and collective values.
The three rows in table 2 distinguish among clinical
interventions for people who already have problems (reactive /indicated),
programs for people who are at high risk of developing health complications
(proactive/high risk), and health promotion initiatives for the population at
large (proactive/universal). The table informs the analysis that follows. We
discuss typical expectations, critical formulations and critical practice for
interventions with individuals, groups and communities along these dimensions.
Interventions
that Promote Individual Wellness
Typical expectations. In working with individuals, health psychologists are
expected to help with a variety of issues, ranging from reactive to proactive
interventions. We distinguish in table 2 among indicated, high risk, and
universal populations.
Health psychologists often engage in reactive
interventions in medical settings. Services offered directly to patients or
through consultation with other professionals include coping with acute or
chronic pain, compliance with medical treatments, rehabilitation towards
restoration of physical functioning, preparation for surgery and stressful
medical procedures, and psychosocial rehabilitation (Belar & Deardoff,
1995; Bennett, 2000). Proactive interventions occur usually in worksites,
community health centres or educational institutions. They usually take the
form of programs to stop smoking or drinking or to improve diet. We note below
some reservations with respect to individual and group interventions.
Critical formulations. Institutional settings like hospitals prescribe and
perpetuate roles for all the players within it. The sick role of the patient
diminishes his or her power and self-determination, whereas the role of expert
of physicians increases their ability to make decisions for others. In such
hierarchical places, all the actors are at risk. Some, like patients and low
status workers, are at risk for reduced ability to control their lives and
environments. Others, like high status professionals, are at risk for abusing
power and engaging in patronizing behaviour. AThe dominance of the medical profession, for instance, is expressed and
reinforced through the micro level of medical encounters. In the hospital, the
consultant's round has long been an expression of power over medical students,
nurses, and patients@ (Hardey, 1998, pp. 83-84).
In the interaction between
patients and medical professionals, the power and expertise of the latter runs
the risk of diminishing the self-determination of the former in multiple ways.
First, they do so by prescribing treatments without adequately consulting
patients or explaining the basis of the decision in accessible language.
Second, by failing to elicit and patiently explore patients' lived experience
of their illness, and the feasibility of adhering to the prescribed treatment
within the context of patients' diverse life circumstances. Third, by creating
distance and fostering asymmetrical relationships among themselves and their
patients, often as a shield against doctors' own feelings of helplessness in
the face of human suffering that cannot be easily alleviated. These are but a
few examples of disempowering treatment of patients which has received growing
recognition in the sociology of health and illness. Numerous studies
demonstrate the control of physicians over the content, length, and nature of
interaction with patients (Curtis, 2000; Samson, 1999; Weitz, 1996). It has
also been found that many physicians promote stereotypical roles for women and
that they react in a defensive and even hostile manner when challenged by their
female patients (Hardey, 1998). (For an overview of encounters between
health-care professionals and patients, see also Crossley, 2000). In this context, the psychologist is at risk for
abusing his or her relative high status, and for being discounted by medical
practitioners who run hospitals and assume ultimate decision making powers with
respect to patients.
We are not contesting the need to apply proven
strategies of coping and behaviour modification to client health issues.
However, we must remember that all of this takes place in a context suffused by
power differentials where the perspective of the client or other health
professionals, such as physiotherapists or social workers, may be lost due to
their relative lack of power. There is, then, the physical construction of
illness and the social construction of illness (Freund & McGuire, 1999). As
Radley (2000) reminds us, "it is not just what it means to be ill that is
socially defined, but what it means to be treated and, make a good
recovery" (p. 302)
The chosen method of helping is not only determined by
the best available scientific evidence, but is also mediated by the meaning of
the condition negotiated among patient and multiple professionals. Thus, for
example, a patient's complaint of physical pain may not conform to known
anatomical structures. This may lead to some scepticism regarding the
legitimacy of the complaint, and to a hypothesis of a possible underlying
psychological mechanism. An inability to find a clear organic basis for a
patient's complaint often results in various such hypothesis being generated
and perpetuated by different professionals. If a law suit is pending
against an employer or the state, diagnosis becomes even more complicated.
The point of this hypothetical situation is to show
how complicated assessment and choice of treatment can become. When we combine
all of the contextual factors implicated in diagnosis and treatment, a fairly
complicated picture emerges. A critical appraisal of the situation would take
into account power differentials in problem formulation, risk of diminished
self-determination of patients, potential labeling of patients, and access by
patients to needed resources. In synthesis, critical psychology adds another
dimension to helping. Selection of best cognitive or behavioural strategies is
not enough (Crossley, 2001a, b). Patient participation and empowerment in
method of help are also crucial.
However helpful clinical interventions might be,
health psychology has been criticized for concentrating too much on individuals
and for preferring a reactive mode of intervention. According to Winett, "to be effective health psychologists need to adopt an
intervention orientation more diverse in terms of timing and level than their
apparent preference for tertiary prevention with clinical, individual-level interventions" (1995, p. 344). Studies show that remedial
interventions for high risk conditions such as obesity, high cholesterol, and
smoking, are not very effective (Smedley & Syme, 2000; Wilkinson, 1996).
Once entrenched, these patterns of behaviour are hard to change. In any case,
even when they are effective, they do not address the constant flow of new
cases with such adverse conditions.
The critique leveled against health psychology is not
only that it responds late to conditions, but also that it addresses
individuals and not societal structures. The proactive approach that centres on
individuals at risk is incapable of reducing incidence, or the number of new
cases of a problem. As Wilkinson (1996) noted,
Sometimes it is a matter of providing screening and
early treatment, other times of trying to change some aspect of lifestyle, but
always it is a matter of providing some service or intervention. This applies
not just to health, but also to studies of a wide range of social, psychological,
developmental and educational problems. What happens is that the original
source of the problem in society is left unchanged (and probably unknown) while
expensive new services are proposed to cater for the individuals most affected.
Each new problem leads to a demand for additional resources for services to try
to put right the damage which continues to be done. Because the underlying flaw
in the system is not put right, it gives rise to a continuous flow, both of
people who have suffered as a result, and of demands for special services to
meet their needs. (p. 21).
Critical practice. Opportunities for helping are present at the individual, group/
organisation,
and community/societal levels. At each level, we propose to use a partnership
model. A partnership ensures that clients and all other professionals are
heard. Furthermore, it implies that decision-making power will be shared, and
that the wishes of medical patients will be given proper priority.
We consider here the case of patients in a rehabilitation
hospital, following serious accidents, strokes, or exacerbation of pre-existing
conditions such as Multiple Sclerosis.
Following
the initial phase when one is simply grateful to be alive, the reality of
decreased mobility and difficulties with various aspects of daily living, often
sets in. Sometimes it is a temporary condition that is expected to improve with
time and physical therapy, other cases may require adjustment to a permanent
change in status, whereas in some situations, further decline in health and
physical functioning is to be expected. Notwithstanding these important
differences, affected individuals often become psychologically vulnerable.
The overarching goal of rehabilitation settings is to
enable individuals to return to previous levels of functioning, resume roles,
and re-integrate into society with as little disruption as possible.
Undoubtedly, this is a desired outcome for most patients, and serves as a major
motivating factor for the hard work they invest in their various therapies.
Notwithstanding the commitment and dedication of most rehabilitation
professionals and the vital work that they do with patients, the elevated value
attributed to physical independence in such settings should be questioned.
Occupational and physical therapists work with their patients towards enhancing
the latter's ability to independently carry out activities of daily
living. Whereas most people would
prefer to be as independent as they can in self-care, needing assistance, even
with the most intimate tasks of daily living, is not tantamount to losing
autonomy and control. Deconstructing such words as independence and autonomy
from a disability rights-perspective, can have a profoundly empowering effect
on the lives of individuals with severe physical impairments. This is
exemplified by the following quote by a disability rights activist:
We believe fundamentally that all individuals have the
right to live independently in the community regardless of their disability. But
it is important to note the sense in which we use the term 'independence,= because it is crucial to everything we are saying. We
do not use the term 'independent' to mean someone who can do everything for themself,
(sic) but to indicate someone who has taken control of their life and is
choosing how that life is led....it can be applied to the most severely
disabled person who lives in the community and organizes all the help or 'care'
they need as part of a freely chosen lifestyle. The most important factor is
not the amount of physical tasks a person can perform, but the amount of
control they have over their everyday routine. The degree of disability does
not determine the amount of independence achieved (Brisenden, 1998, pp. 26-27).
We
are not suggesting here that occupational and physical therapists should cease
to help people restore physical abilities and promote unaided functioning.
Rather, it is the unquestioned assumption that physical independence should be
attained at all costs, with which we take issue.
If a person does not find meaning in preparing
breakfast for herself, a task that may take her 45 minutes and drain her of
energy that may already be in short supply, perhaps another person could do it
for her in 5 minutes. A rehabilitation patient in a setting we worked in
jokingly spoke of the routines he goes through in order to appease his treating
therapists who decided that he should participate in 'breakfast group'. A
stroke had left this man with significant physical impairments, while his
cognitive functioning remained relatively intact. Whilst it was very clear to
him that he would not be attending to his own breakfast at home given the time
and energy that this required of him, he felt it necessary to be a 'good
patient', thereby avoiding conflict which may be more trouble than it is worth.
This man was willing to play the game and had maintained his sense of humour in
the process. However, making such decisions on behalf of patients is what truly
robs people of dignity and control over their lives.
Proactive interventions with individuals have to
address the societal sources of smoking, drinking, binging, and sitting for too
long. To begin addressing the societal causes of disease it is important to
politicize community members. It can be empowering for a young woman with an
eating disorder to understand and take action against the media. Lyons (2000)
asserts that media representations of health and illness have been surprisingly
overlooked by health psychologists. She makes a cogent argument for a critical
analysis of media images. In addition to affecting people's beliefs and
understanding of health and illness, media images can influence people's
attitudes towards certain subgroups of the population, as well as mediating
individuals' own lived experience of illness. She further reminds us that
"examinations of what is not represented in the media are also extremely
beneficial"(p. 356), referring to the preponderance of images of young
female bodies versus the invisibility of disabled bodies, aging bodies, etc.
Feminists use anger toward societal oppression in
empowering ways (Riger, 2000). So do narrative therapists and advocates of just
therapy (Community Mental Health Project, 1998). There is a need to connect
corporate agendas with personal suffering. In a smoking prevention program with
children and youth we discussed at length the commercial roots of addictions.
Children in the program protested in shopping malls against tobacco companies
and made a presentation to city council on the subject (Prilleltensky, Nelson,
& Sanchez Valdes, 2000). These are examples of linkages between personal
risk factors and their societal origins. We have to make these connections for
the benefit of people who are at risk today and for the benefit of those who
will be at risk tomorrow if corporations continue to infect the public with
toxic products. As critical health psychologists we have to ask ourselves
whether we want to support the status quo by treating its victims, or whether
we want to join with them to challenge noxious consumerism.
Interventions
for Group and Organisational Wellness
Typical expectations. Work with groups and organizations can also be
reactive or proactive. Health psychologists can work with patients in support
groups or exercise programs, and they can assist worksites to improve the
social climate and reduce stress and conflict. Many health psychologists assist
organizations to improve the health of their employees through lifestyle
changes and exercise.
Critical formulation. In the meso context of hospitals, clinics, and work
settings, power and control affect health in significant ways as well. In the
Whitehall studies, Marmot and his colleagues followed the health of thousands
of British civil servants for three decades (Marmot, 1999; Marmot, Siegrist,
Theorell, & Feeney, 1999). The participants were all middle class people
who enjoyed relative affluence. Although all of them could be considered middle
class, the 25 year follow up study showed that those in lower positions had a
four times higher mortality rate than those in administrative positions. There
was a clear correlation between level of control over the work environment and
several measures of disease, with those lower on the scale of control
experiencing poorer health. When participants were divided into four employment
grades, there was a distinct and gradual escalation in health from the lower
grade to the higher grade. As Marmot (1999) noted,
There are abundant data
showing a link between poverty and ill health. These results from Whitehall
have influenced us in coming to the view that inequality is also important. The
problem of inequality in health is not confined to the poorest members of
society but runs right across the social spectrum. In Whitehall the social
gradient was seen not only for total mortality, but for all the major causes of
death, including coronary heart disease and stroke. (p. 12)
Studies conducted by Marmot and others suggest
that the work environment affects health through three psychological
mechanisms. The first relates to levels of demand and control, whereby higher
demands and lower levels of control affect health negatively. The second mechanism
refers to the effort-reward imbalance, and the third to the level of social
support (Marmot et al., 1999).
From a critical psychology
perspective, we see that the amount of power experienced by workers is directly
related to health and mortality. How is this power attained, and how it may be
challenged and redistributed is a key concern for critical psychologists. The
struggle to distribute power and control equitably within hospitals and work
settings defines a key job for the critical health psychologist.
Hospitals and work settings are laden with power
conflicts. It would be a mistake to intervene in these types of organizations
without considering the effects of the political environment. Unless the health
psychologist recognizes the political role that he or she might be fulfilling,
undesirable consequences may ensue. Interventions to improve the working
climate may mask underlying conflict, to the direct benefit of management.
Surely reducing stress is a meritorious cause, but diverting attention away
from the roots causes of that stress hinders the cause of health. As we can
see, the health psychologist is caught in a bind, much like the organizational
psychologist who is asked to improve working conditions. On one hand, research
clearly suggests that reduced stress is good for health. But on the other hand,
superficial attempts to alleviate conflict may divert attention from more
fundamental roots of discomfort.
Marmot and colleagues (1999) clearly showed that lack
of control at work is related to increased levels of illness. Launching
initiatives that restore employee control across the board is a good health
intervention for as long as it is not temporary or superficial. The health
psychologist has the difficult job of discerning whether an intervention will
benefit workers unequivocally or only temporarily, and whether the net effect
of the program is not worker appeasement.
Critical practice. We consider possible interventions in hospital and work settings in
turn. Because of the prescribed scripts that patients and doctors are expected
to follow in a total institution like a hospital, we regard both of these
groups as sites for action. Of course not all patients and professionals engage
in stereotypical roles of sick and helper, but the evidence is such that people
in hospitals often behave in hierarchical and constraining ways. Hence, at the
group/organizational level we recommend interventions to improve communication
between professionals and patients. Research suggests that communication
between practitioners and patients is often faulty. A study by Beckman and
Frankel (1984) confirms this claim. In a sample of seventy four office visits,
only 23% of the patients had a chance to finish their explanations of concerns.
Doctors were found to interrupt patients in 69% of the visits. On average,
doctors interrupted patients after they had spoken for only 18 seconds. In
another study, West (1983) reported that patient-initiated questions were
discouraged. Out of a total of 773 questions asked in 21 medical encounters,
only 9 % of the questions were initiated by patients. The use of jargon,
patronizing attitudes, and patient anxiety contribute to miscommunication
between doctors and patients.
While we advocate for assertiveness and communication
training, we should remain skeptical of the potential for such interventions to
make lasting changes. The origins of patriarchal mentality in medical settings
are profound and may not be undone by workshops on communication. Lupton (1994)
cautions that
to assume that the majority of patients, given
appropriate training in communication competencies, will have equal authority
in the doctor-patient relationship is to ignore the structural and symbolic
dimensions of this relationship. Although there is limited opportunity for
patients to assert their agency, the whole nature of the doctor-patient
relationship and the healing process rests on the unequal power balance and
asymmetry of knowledge between patient and doctor. (p. 59)
It
is clear that more fundamental changes in the medical establishment will have
to occur to democratize the patient-doctor relationship. Work towards that
goal, however, does not invalidate the need to empower patients while they are
the subject of medical investigations and interventions.
The health psychologist can also intervene in work
settings. Solidarity among workers is very important. It is a source of social
support and even empowerment. Not all aggression in the workplace comes from
above. Horizontal violence is quite prevalent (Keashley, 1998). Programs that
address workplace bullying and that build cohesion among workers can have
substantial health benefits. By linking health with solidarity we are
politicizing wellness and supporting cohesion among workers.
We touched here on hospital and workplace actions.
Table 2 mentions other possible interventions with groups and organisations. We
move now to consider tasks at the community and societal levels.
Interventions
for Community and Societal Wellness.
Typical expectations. Psychologists participate in health promotion
campaigns through research, education, and intervention. They may facilitate
the dissemination of information through regional health authorities or contribute
to the development of public policy.
Critical formulations. The macro economic and psychosocial environment where
we live have direct repercussions for health and quality of life. Consider the
following examples provided by Wilkinson (1996). A child born and raised in
Harlem has less chances of living to 65 years old than a baby born in
Bangladesh. Also in the US, life expectancy is 7 years longer for whites (76
years) than for African Americans (69 years). In lower social classes, infant
mortality in Sweden (500 per 100,000) is less than half the rate in England
(1250 per 100,000). Because of more egalitarian income distribution, the life
expectancy of Japanese people increased by 7.5 years for men and 8 years for
women in 21 years. This dramatic increase took place between the years 1965 and
1986. Japanese people experience the highest life expectancy in the world, near
80 years, in large part because in that period of time they became the advanced
society with the narrowest income differences. Communities with higher levels
of social cohesion and narrow gaps between rich and poor produce better health
outcomes than wealthier societies with higher levels of social disintegration.
When probability of death
between ages 15 and 60 is compared between richer and poorer countries, the
former have outcomes that are about three times better than the latter. Reasons
for death include infections, perinatal, nutritional, maternal, cardiovascular,
cancer, respiratory disease and other external causes (see Marmot, 1999, p. 6).
Lack of shelter and sanitation are major causes of killing diseases around the
world. Feuerstein (1997) reports that between 1988 and 1991, in 34 of the 47
least developed countries, only 46% of the population had access to safe water.
The atrocious effects of poverty on health have been documented extensively.
They remind us that health is not only the effect of health care but of living
conditions.
Within countries, the poor,
the unemployed, refugees, single parents, ethnic minorities and the homeless
have much lower rates of health than more advantaged groups. This applies not
only to poor countries, but to rich countries as well. Homeless people in
western countries, for example, are 34 times more likely to kill themselves than
the general population, 150 times more likely to be fatally assaulted, and 25
times more likely to die in any period of time than the people who ignore them
on the streets (Shaw, Dorling, & Smith, 1999). There is no question that
the macro-environment influences health in potent ways.
But the body of knowledge
compiled by Marmot and Wilkinson (1999) clearly indicates that, in addition to
economic prosperity, equality and social cohesion are also powerful
determinants of health. Indeed,
In the developed world, it is
not the richest countries which have the best health, but the most
egalitarian....Looking at a number of different examples of healthy egalitarian
societies, an important characteristic they all seem to share is their social cohesion...The
epidemiological evidence which most clearly suggest the health benefits of
social cohesion comes from studies of the beneficial effects of social networks
on health. (Wilkinson, 1996, pp. 3-5)
As Wilkinson observed, social cohesion is
mediated by commitment to positive social structures, which, in turn, is
related to social justice. Individuals contribute to collective well-being when
they feel that the collective works for them as well. Social cohesion and
coherence are Aclosely related to social justice@ (Wilkinson, 1996, p. 221). The critical psychologist
faces a serious challenge in trying to incorporate these lessons into his or
her practice. We distill below some of the implications for action.
Critical practice. Within the reactive and indicated framework, there is
much that needs to be done to ensure that minorities have adequate access to
health care. AA lack of access can have deadly consequences@ (Weitz, 1996, p. 61). Advocacy, lobbying, and
solidarity partnerships are vehicles to pressure governments to act on behalf
of vulnerable populations. Although the formal medical system is not the only
means to health, it is a social resource that needs to be distributed equally
among all. We see this type of political work as integral to the work of
critical health and community psychologists. Feuerstein (1997) outlines several
strategies for collaborating with the poor for improved health, including
financial services and credit for the poor.
The practice of health promotion at the social and
community levels is appealing, but only insofar as it includes a critique of
capitalist market rules. We link health promotion to a critique of corporate
ruling because, otherwise, we focus on individuals and neglect the societal and
market origins of illness (Kawachi, Kennedy, & Wilkinson, 1999; Kim,
Millen, Irwin & Gersham, 2000; Korten, 1995). As Lupton (1994) noted, Aalthough the health promotion perspective relies
heavily on a critique of the biomedical model, it fails to challenge the hegemony
of ideologies that deflect the responsibility of health maintenance from the
state to the individual@ (p. 57). Therefore, we advocate a combined approach
that couples health promotion to activities designed to challenge corporate
ruling of health and illness (Crossley, 2001a, b). What we watch, eat, drink,
and breath have a lot to do with global capitalism, an economic structure that
has proven detrimental to global health (Feuerstein, 1997; Korten, 1995; Marmot
& Wilkinson, 1999).
Re-inventing ourselves as advocates, social critics,
community leaders and psychologists at the same time is a necessity that may
not sit well with health psychologists. However, to remain at the level of
reactive or person-centred interventions is to deny a massive body of evidence
linking social and economic structures to physical and psychological health.
Critical health psychology is well positioned to break interdisciplinary
barriers and address wellness in a truly ecological way.
Conclusion
What health psychologists do mostly is not necessarily
what helps the most. Whereas most health psychologists work with individuals
already affected or at risk for health problems, evidence suggests that the
most promising ways to promote overall health is to work with entire
communities in a proactive fashion (Kaplan, 2000; Smedley & Syme, 2000).
Critical and community psychologists used to argue that the focus on the
individual is not enough. New information indicates that working with groups at
risk is not good enough either. By the time groups of people develop symptoms,
it is extremely difficult to revert unhealthy behavioural patterns.
Furthermore, most risk conditions do not reside within the individual but
within the social and physical environments. As a result, preventive efforts
for people at risk have proven only minimally effective (Kaplan, 2000;
Wilkinson, 1996). This was the rather disappointing result of the largest trial
of behavioural change ever conducted. The Multiple Risk Factor Intervention
Trial (MRFIT) Aattempted to change diet, smoking and exercise among
white men identified as being in the highest 10 per cent of risk for coronary
heart disease. Despite concentrated efforts over six years they only succeeded
in making minimal changes@ (Wilkinson, 1996, p. 64). The implication of these
findings is that risk factors are in themselves symptoms of more profound
causes of disease that most behavioural interventions fail to address. In other
words, these interventions do not address the causes of the causes, but only
some outcomes of deeper causes.
Evidence from social determinants of health indicates
that overall wellness is predicated on sufficient material resources, equality
in distribution of resources, and social cohesion. These three factors are the
domain of proactive universal interventions for community and societal
wellness. Large international epidemiological studies demonstrate that each of
these factors is a necessary but not a sufficient precursor of overall health.
For optimal health to occur, they have to operate simultaneously. For critical
health psychologists the implication is clear: we cannot fragment wellness into
economic, social and psychosocial health; they work in synchronicity, and so
should we.
References
Beckman, H., & Frankl, R.
M. (1983). The effects of physician=s behaviour on the
collection of data. Annals of Internal Medicine, 101, 692-696.
Belar, C., & Deardorff, W.
(1996). Clinical health psychology in medical settings. Washington DC:
APA Books.
Bennett, P. (2000). Introduction
to health psychology. Philadelphia: Open University Press.
Bennet, P., & Murphy, S.
(1997). Psychology and health promotion. Philadelphia: Open University
Press.
Brisenden, S. (1998).
Independent living and the medical model of disability. In T. Shakespeare
(Ed.). The Disability reader: Social science perspective. Cassell:
London.
Chamberlain, K. (2000).
Methodolatry and qualitative health research. Journal of Health Psychology, 5(3),
285-296.
Community Mental Health Project.
(1998). Companions on a journey: The work of the Dulwich Centre Community
Mental Health Project. In C. White & D. Denborough (Eds.). Introducing
narrative therapy. Adelaide: Dulwich Centre Publications.
Crossley, M. L. (2000). Rethinking
health psychology. Open University Press, Buckingham.
Crossley, M. L. (2001a).
Rethinking psychological approaches towards health promotion. Psychology and
Health, 16, 161-177.
Crossley, M. L. (2001b). Do we
need to rethink health psychology? Psychology, Health, and Medicine, 6, 243-255.
Curtis, A. (2000). Health
psychology. London: Routledge.
Eimer, B., & Freeman, A.
(1998). Pain management psychotherapy. New York: John Wiley & Sons.
Feuerstein, M. (1997). Poverty
and health. London: Macmillan.
Fox, D. & Prilleltensky,
I. (Eds.). (1997). Critical psychology: An introduction. London: Sage.
Freund, P., McGuire, M.
(1999). Health, illness, and the social body: A critical sociology. Upper
Saddle River, NJ: Prentice Hall.
Hardey, M. (1998). The
social context of health. Philadelphia: Open University Press.
Kaplan, R. (2000). Two
pathways to prevention. American Psychologist, 55, 382-396.
Kawachi,
I., Kennedy, B., Wilkinson, R. (Eds.). (1999). The society and population health
reader: Income inequality and health. New York, NY:
The New Press.
Kim,
J. K., Millen, J. V., Irwin, A., & Gersham, J. (Eds). (2000). Dying for
growth: Global inequality and the health of the poor. Monroe, ME: Common
Courage Press.
Keashley, L. (1998). Emotional abuse in the workplace:
Conceptual and empirical issues. Journal of Emotional Abuse, 1, 85-117.
Korten, D. C. (1995). When
corporations rule the world. San Francisco: Berret-Koehler.
Lupton, D. (1994). Toward the
development of critical health communication praxis.
Health Communication, 61, 55-67.
Lyons, A. C. (2000). Examining
media representations: Benefits for health psychology. Journal of Health
Psychology, 5(3), 349-358.
Marks, D. (2002). Freedom,
responsibility and power: Contrasting approaches to health psychology. Journal
of health Psychology, 7(1), 5-19.
Marmot, M. (1999).
Introduction. In M. Marmot and R. Wilkinson (Eds.). Social determinants of
health (pp. 1-16). New York: Oxford.
Marmot, M., Siegrist, J.,
Theorell, T., & Feeney, A. (1999). Health and the psychosocial environment
at work. In M. Marmot and R. Wilkinson (Eds.). Social determinants of health
(pp. 105-131). New York: Oxford.
Marmot, M., & Wilkinson,
R. (Eds.). (1999). Social determinants of health. New York: Oxford
University Press.
McCubbin, M. (2001). Pathways
to health, illness and well-being: From the prespective of power and control. Journal
of Community and Applied Social Psychology, 11(2), 75-81.
Murray, M., & Chamberlain,
K. (Eds.). (1999). Qualitative health psychology: Theory and methods. Thousand
Oaks, CA: Sage.
Nelson, G., Prilleltensky, I. & Peters, R. D.
(1999). Prevention and mental health promotion in the community. In W. L.
Marshall, & P. Firestone (Eds.), Abnormal psychology: Perspectives
(pp. 461-478). Scarborough, Ontario: Prentice Hall Allyn & Bacon Canada.
Nicholas, M., Molloy, A., Tonkin, L., & Beeston,
L. (2000). Manage your pain. Sydney: ABC Books.
Petersen, A. (1994). In a
critical condition: Health and power relations in Australia. St. Leonards,
NSW: Australia.
Prilleltensky, I. (1999).
Critical psychology foundations for the promotion of mental health. Annual
Review of Critical Psychology, 1, 95-112.
Prilleltensky, I., &
Nelson, G. (in press). Doing psychology critically: Making a difference in
diverse settings. London: Macmillan.
Prilleltensky, I., Nelson, G.,
& Peirson, (2001a). The role of power and control in children=s lives: An ecological analysis of pathways towards
wellness, resilience, and problems. Journal of Community and Applied Social
Psychology, 11, 143-158.
Prilleltensky, I., Nelson, G.,
& Peirson, (2001b). Promoting family wellness and preventing child
maltreatment: Fundamentals for thinking and action. Toronto: University of
Toronto Press.
Prilleltensky, I., Nelson, G.,
& Sanchez Valdes, L. (2000). A value-based approach to smoking prevention
with immigrants from Latin America: Program evaluation. Journal of Ethnic
and Cultural Diversity in Social Work, 9(1-2), 97-117.
Radley, A. (2000). Health, psychololgy, embodiment and
the question of vulnerability. Journal of Health Psychology, 5(3), 297-304.
Riger, S. (2000). Transforming
psychology. New York: Oxford University Press.
Samson, C. (1999). The physician
and the patient. In C. Samson (Ed.). Health studies: A critical and cross
cultural reader (pp. 179-196). Oxford: Blackwell.
Shaw, M., Dorling, D., &
Smith, G. (1999). Poverty, social exclusion, and minorities. In M. Marmot and
R. Wilkinson (Eds.). Social determinants of health (pp. 211-239). New
York: Oxford.
Smedley,
B., & Syme, L. (Eds.). (2000). Promoting health: Intervention strategies
from social and behavioral research. Washington, DC: National Academy
Press.
Stam, H. (2000). Theorizing healthh
and illness: Functionalism, subjectivity, and reflexivity. Journal of Health
Psychology, 5(3), 273-283.
Stainton-Rogers, W. (1996).
Critical approaches to health psychology. Journal of Health Psychology, 1,
65-78.
Taylor, S. (1995). Health
psychology (3rd.ed.). New York: McGraw Hill.
Tones, K. (1996). The anatomy
and ideology of health promotion: Empowerment in context. In A. Scriven and J.
Orme (Eds). Health promotion (pp. 9-21). London: Macmillan.
Weitz, R. (1996). The
sociology of health, illness, and health care: A critical approach. New
York: Wadsworth/ITP.
West, C. (1983). AAsk
me no questions...@: An analysis of queries and
replies in physician-patient dialogues. In S. Fisher and A. Todd (Eds.) The
social organisation of doctor-patient communication (pp. 75-106). Norwood,
NJ: Ablex.
Wilkinson, R. (1996). Unhealthy
societies: The afflictions of inequality. London: Routledge.
Wilkinson, S. (2000). Feminist
research traditions in health psychology: Breast cancer research. Journal of
Health Psychology, 5(3), 359-372.
Winett, R. (1995). A framework
for health promotion and disease prevention programs. American Psychologist,
50, 341-350.
Table 1
Health
Psychology Practice from a Critical Psychology Perspective
|
Critical
Psychology Tenets |
Possibilities
for Action |
|
Values
for -
personal wellness -
relational wellness -
collective wellness |
Content:
Balance prevalent emphasis on autonomy with concern for caring and compassion
and interdependence. Consider power differentials in hospital settings and
their impact on patients=
empowerment and self-determination. Social cohesion, collaboration and
democratic participation at community level benefit population health. Process:
Show caring and compassion for citizens seeking service, respect their
social identities, and foster their ability to pursue personal goals in light
of chronic illness or disability. Involve community members in civic and
health related activities. Create partnerships with community groups to
achieve justice in health care. |
|
Assumptions
about -
good life -
good society -
knowledge -
ethics -
role of worker -
role of client |
Content:
Ensure that definition of problems and health includes voice of citizens
seeking help and is not circumscribed to professional opinion. Consider role
of corporate profit making in health problems. Promote focus on strengths and
competencies of person as perceived and described by person seeking help.
Beware of the pursuit of pathology prevalent in hospital settings. Process: Act as
resource collaborator instead of removed expert. Engage citizens in active
roles throughout the process of help or self-help. Consider alternatives to medical
treatments such as health promotion activities related to diet and lifestyle. Promote non-professional
interventions such as mutual-help groups. Afford people seeking help
meaningful opportunities to present their point of view concerning their health.
Renew informed consent often and solicit input from patients as to direction
and aims of helping relationship. Respect privacy of patients in medical
settings. |
|
Practices
-
problem definition -
scope of intervention -
time of intervention |
Content:
Consider approaches that go beyond reactive and indicated
interventions and that are proactive in nature. Address social and economic
origins of ill-health and maldistribution of resources and health in society.
Process:
Collaborate with advocacy and social justice groups in addressing the
health needs of the entire population. Create solidarity partnerships with
community groups affected by ill-health. Promote political education and
social action leading to health promoting cultures and organisations. |
Table from
Prilleltensky and Nelson (2002).
Table 2
Ecological
Levels, Values, and Potential Critical Psychology Interventions in Health
Settings
|
Timing
and Population of Intervention |
Values and
Ecological Levels |
|
|
Values
for Personal Wellness self-determination,
protection of health, caring and compassion |
Values
for Relational Wellness collaboration, democratic participation, and respect for
diversity |
Values for
Collective Wellness support
for community structures, social justice |
|
|
Individual
Wellness |
Group
and Organisational Wellness |
Community
and Societal Wellness |
|
Reactive
Indicated |
*
Self-determination in rehabilitation * Power sharing
in treatment plans for coping with illness and chronic pain |
*
Assertiveness training for hospital patients dealing with professionals *
Communication training for professionals dealing with vulnerable patients |
*
Securing access of minorities, refugees and the poor to all health services *
Lobbying for funding of health services in deprived areas |
|
Proactive
High Risk |
*
Smoking cessation with emphasis on exploitation of community by tobacco
companies * Diet and
exercise program for overweight people with emphasis on ill effects of
consumerism |
*
Exercise program for disadvantaged populations at high risk for heart disease *
Organisational interventions to reduce stress in patients and staff |
* Self-help/mutual aid and support groups for
people caring for disabled family members * Community wide programs to improve diet,
lower alcohol consumption and increase exercise |
|
Proactive
Universal |
*
Self-instruction guide on breast examination *
Self-instruction guide on HIV prevention |
*
Organisational development to improve working atmosphere * Bill
of rights and responsibilities for patients and staff in hospitals |
* Critique
and boycotts of media and corporations making profits at expense of
population health *
Promote social cohesion and egalitarian social policies |
Table from
Prilleltensky and Nelson (2002).