Full text of DOI:10.1046/j.1365-2850.2000.00264.x

Journal of Psychiatric and Mental Health Nursing, 2000, 7, 59–67
Anti oppressive practice: a route to the empowerment of people
with dementia through communication and choice
GEOFFREY W. MARTIN rgn rmn bsc MA & DENNIS YOUNGER rmn bsc
University of Teesside, School of Health, Middlesbrough TS1 3BA, UK
Correspondence:
G. W. Martin
School of Health
University of Teesside
Middlesborough
TS1 3BA
MARTIN G. W. & YOUNGER D. (2000) Journal of Psychiatric and Mental Health
Nursing 7, 59–67
Anti oppressive practice: a route to the empowerment of people with dementia
through communication and choice
This short study looks at the issue of anti oppressive practice and the way that it relates
to the care of people with dementia. In particular it considers ways in which people can
be empowered and given choices around aspects of day-to-day living in a care setting. The
study took place over a period of 6 months and utilized the Dementia Care Mapping
UK
(DCM) observation process to assess the level of well being of residents in the setting
studied. The results can only be seen as a first stage in the process of understanding ways
in which people with dementia may be empowered. It is demonstrated that a change of
practice developed over the 6 months between the two observation periods. Areas such as
communications and day-to-day activities are examined to identify both problems and
strategies for such change. The conclusion highlights the need to continue the mapping
exercise as a way of ensuring that change is not only maintained but also advanced.
Keywords: anti oppressive practice, care mapping, dementia, empowerment, observation,
research
Accepted for publication: 12 November 1999
day patient settings and highlights some problems of using
the technique as an audit tool. Wilkinson’s (1995) pilot
Introduction
This study, part of work in progress, examines the concepts
of anti oppressive practice and empowerment as related to
the care of people with dementia. The literature around
this area of care has, until recently, largely ignored the
rights of people with dementia to any form of autonomy
and it is to this omission that the paper is addressed. In
recent years we have seen a body of work building up
around the rights and ‘personhood’ of people with
dementia (Kitwood 1995, Kitwood 1997, Marshall 1997,
Rafferty 1997) and there is a growing body of work which
highlights the role ageism plays in the care of older people
study points the way to further research in the area and
Williams & Rees (1997) demonstrate a clear link between
DCM and improving quality of care. It is important that
we now consider ways in which the concepts discussed can
bring about change in nursing practice, particularly with a
view to the promotion of anti oppressive practice. There
has been a few studies that have looked at empowerment
and dementia (Chapman 1993, Goldsmith 1996), and this
paper seeks to add to this work.
The model of anti oppressive practice discussed in this
study relies, in the main, on the interpersonal communica-
tion processes which arise between the nurse and the
patient/resident as reflected in the results of a Dementia
Care Mapping exercise. The objective of the study is to see
if a DCM exercise can bring about improvements in prac-
tice, related to patient choice and control, in one particu-
(
Bytheway 1995). A number of research papers have used
a similar DCM method to good effect (Brooker & Payne
995, Wilkinson 1995 and Williams & Rees 1997). Each
1
uses a behavioral analysis approach in different care set-
tings. Brooker & Payne (1995) looks at both in patient and
©
2000 Blackwell Science Ltd
59

G. W. Martin & D. Younger
lar care setting. Communication, according to Killick
and therefore defined and manipulated in the interests of
that group alone. The relationship between the health pro-
fessional and the patient is double edged, consisting of
elements of care and control, both potentially empowering
and potentially oppressive (Thompson 1993). Ideologies
which maintain the responsibility for patent empowerment
solely on professionals may serve to legitimate the status
quo in the unequal balance of power, and so justify, protect
and reinforce current social arrangements of power. One
means by which this can happen is by the establishment
of ‘norms’ which construct a notion of the ‘normal’, so
establishing a standard to measure deviance from that
norm. The terms ‘normal grieving’, ‘normal relationships’,
‘normal behavior’, for instance, act as powerful ways of
legitimating practice. Stereotypes of the ‘abnormal’ are
therefore powerful tools of ideology and are thus signifi-
cant obstacles to anti oppressive practice (Thompson
1993). It is through medical nursing discourse that power
relations are constructed which have the ability to create
an ‘outgroup’ of people, be they black, homosexual men
or lesbians, old, demented, etc., defined in negative terms
and assigned an inferior status. By way of example,
Thompson points to the use of the terms ‘dependency’
and ‘frailty’, to describe older people. Such terms imply
a medical model which focuses on physical incapacity,
decline and dysfunction of the person rather than their
social diversity. Anti ageist practice, he maintains, should
focus instead on empowerment through advocacy rather
than adjustment to infirmity. Thompson (1993) concludes
that,
(1997), must take pride of place in our design and deliv-
ery of care for persons with dementia.
For nurses to act as empowerers, a new approach must
be adopted. This approach depends for its success on the
capacity of nurses to be prepared to work with patients at
an empathetic, anti oppressive level that overrides aspects
both of paternalism and rigid professionalism. Nurses must
attempt to overcome disempowering situations, despite the
pressures imposed upon them to conform to the traditional
definition of their roles. The nurse, patient and other health
care professionals are faced with a complex set of inter-
locking relationships within which communication takes
place. The extent of control will depend very much on their
relative status. For anti oppressive practice to become pos-
sible the balance will have to shift in favor of the patient.
It is the nurse who is most able to bring about this shift,
by insuring the patient’s boundaries of knowledge and
control are extended. This shift can be seen as a cultural
change, similar to that outlined by Kitwood (1995) for
people with dementia where the emphasis is placed on
valuing the ‘personhood’ of the patient. The discussion
should be focused on this change of culture and routes to
change developed (Martin 1997). Issues of communication
cut across all these concepts and will be addressed in the
light of the research results. The discussion will highlight
both barriers and strategies, in an effort to move the debate
forward towards an empowering cultural change. It is
important to address not only the ways that change is pre-
vented from happening but also the ways that change may
begin to occur.
‘Oppression is both a social injustice and a barrier to
self realization and, as such, the removal, reduction and
prevention of oppression are valid and legitimate aims
Anti oppressive practice
.
. .’
Oppressive practice is not just the lot of specific groups,
such as people with dementia, it is more useful to think of
oppression in general terms, as the ability of a powerful
group (health care professionals) to make decision for,
and possibly against the wishes of a less powerful group
However, it is possible that people with dementia will
not have the resources to bring about change which results
in their self empowerment and it is for this reason that
Dalrymple & Burke (1995) believe that it is important to
interrogate rigorously liberally generated values by using
principles, such as empowerment and partnership, that
inform anti oppressive practice. In this way we can take
into account the power differentials involved in moving
forward; change is then more likely to occur.
(patients/clients) (Mullender & Ward 1991). With this in
mind there are certain well defined sections of the com-
munity who face oppression in situations both related, and
not related, to health care. These groups could be seen to
be doubly oppressed within the health care system. Groups
such as women, black and Asian people, disabled people
and lesbian and gay people all face forms of oppression,
which are sometimes hidden and therefore difficult to
identify (Mullender & Ward 1991). These areas of oppres-
sion are central to any discussion of anti oppressive
practice.
Empowerment
A disempowering culture would be one that maintained
a task orientated, paternalistic approach to care, remain-
ing caught in a rigid hierarchical structure. The potential
for devolved decision making, and a holistic approach
to patient care, would therefor be impossible. Moves to
reduce the disempowerment of residents would be difficult
The term empowerment is an ideological concept. It
could be said to remain the property of the holder of power
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Anti oppressive practice
in such a culture, as individual nurses would be unable to
take control of the work environment. Day-to-day working
practices, within this culture, need to be examined there-
fore to ensure that old attitudes do not undermine moves
towards a participatory approach.
Kieffer (1984) conceptualizes empowerment in a devel-
opmental sense that includes both macro and micro con-
siderations. He defines the stages as follows:
(1980) therefore proposes that the analysis of the effect of
power should focus on:
•
local forms of decision making and the techniques
involved;
•
the identification of the processes of ongoing
subjectification;
•
the identification of individuals as the vehicles of
power;
•
era of entry; when the individual’s participation
remains unsure and unknown, even though authority
and power structures at the macro level are becoming
demystified;
era of advancement; when mentorship relationships
begin to emerge and collaboration and mutually sup-
portive problem solving is possible. An understanding
of the situation is gained and mechanisms for action
and choices occur;
era of incorporation; when the permanence and
painfulness of structural or institutional barriers to
self determination are confronted, and organizational,
leadership and survival skills are developed.
era of commitment; when the interaction of new per-
sonal knowledge and skills become part of the reality
and structure of the day-to-day situation.
• the use of a bottom up rather than a top down
approach.
It may be true to say that the powerful are not going to
relinquish their power voluntarily; pressure to effect this
will need to come from other sources. ‘Specific intellectu-
als’, such as nurses, social workers, pressure groups and
teachers would be central actors in any such process of
change.
•
There must be a clear understanding of the ways in
which power operates coupled with the realization that the
nurses’ culture is the product of power structures both
hidden and overt. Only through this understanding will the
hegemony of the present cultural rationality be broken.
This study seeks to identify some of the routes to anti
oppressive practice that nurses can adopt in order to begin
the process of change and so make the empowerment of
people with dementia a possibility. To this end a ‘feedback’
session is included in the exercise which gives the care staff
the opportunity to discuss the results of the mapping and
plan improvements to care where problems are identified.
Very often, once the careers are aware of their potentially
disempowering practice, the process of change can start
with the feedback discussion and develop into a momen-
tum which brings about a change of culture almost
overnight (Moyes & Christie 1998).
•
•
From this we can see that empowerment is just as much
a process of helping individuals to develop some autonomy
of decision making, as it is a process of changing the
culture and organization of the care setting. A readiness to
act to facilitate and engage in the process of the redistrib-
ution of power is central to this awareness. As Gibson
(
1991) puts it, ‘a revolutionary rather than a reformist
approach to problem solving’ is needed which changes the
structure of society rather than integrating change into the
existing structure. Gibson concludes that intervention
needs to take place at the macro level to the conditions that
control, influence and produce health or illness in human
beings. Nurses must be prepared, as part of this process,
to facilitate empowerment within the context of equal
partnership with patients. They must become a ‘resource
mobiliser and advocate’ to ensure that access to resources
are available, and the patient is enabled to make use of
them (Gibson 1991).
It is, according to Foucault (1984), ‘specific intellectuals’
who have the power to either benefit or destroy life. The
nurse is part of this group, able to determine a person’s
choices as well as allocate resources. This power that
nurses have, in itself, can hold the potential to become
empowering. Gilbert (1995) gives a number of examples
where popular knowledge may be used to confront exist-
ing discourse. People with dementia or other mental health
problems may require the nurse’s support to form alliances
with others to challenge prevailing forms of truth. Foucault
Method
Design
A mixture of quantitative and qualitative research based
on a nonparticipatory observation method designed by the
Bradford Dementia Group (1997), has been used. This
research tool has been discussed favorably in a number of
recent papers (Brooker 1995, Williams & Rees 1997). The
quantitative method, called Dementia Care Mapping is a
data gathering tool which gives a clear picture of activity
or nonactivity of the people observed over a given period.
Each activity is divided into behavior categories (BCC) and
given a code (Table 1) for each 5 minute time frame. A sep-
arate score is also given ranging from -5 to +5 according
to the level of ill being or well being (WIB Score) demon-
strated by the resident during the time frame. Total WIB
scores are shown in the form of a graph (Figures 1, 2, 3).
©
2000 Blackwell Science Ltd, Journal of Psychiatric and Mental Health Nursing 7, 59–67
61

G. W. Martin & D. Younger
4
3
3
2
2
1
1
0%
5%
0%
5%
0%
5%
0%
70%
60%
50%
40%
30%
20%
10%
0%
5
0
%
%
-
5
-3 -1
1
1
1
3
3
3
5
5
5
-5 -3 -1
-5 -3 -1
-5 -3 -1
1
3
5
Figure 1
Ted’s WIB Value Profile January and July.
5
4
0%
0%
80%
7
6
5
4
3
2
1
0%
0%
0%
0%
0%
0%
0%
0%
3
2
1
0%
0%
0%
0%
-
5
-3 -1
1
3
5
Figure 2
Hatty’s WIB Value Profile January and July.
7
6
5
4
3
2
1
0%
0%
0%
0%
0%
0%
0%
80%
70%
60%
50%
40%
30%
20%
10%
0%
0
%
-
5
-3 -1
1
3
5
Figure 3
Alice’s WIB Value Profile January and July.
Table 1
The qualitative aspect of this method relates to analysis
of individual ‘personal detractors’ or ‘positive events’
observed during the DCM process. Personal detractors
relate to ways in which care staff and colleagues can rou-
tinely ‘put down’ people with dementia, and are therefore
central to any discussion of oppressive practice (Beavis
Behavior categories (Bradford Dementia Group 1997)
A
Articulation
Interacting with others, verbally or
otherwise
Passively, socially involved
Socially uninvolved, withdrawn
Eating or drinking
B
C
F
Borderline
Cool
Food
K
Kum and go
Independent, walking, standing or
wheelchair moving
1998). Examples may include infantalization, stigmatiza-
L
Labour
Media
Nod, land of
Physical Care
Performing work or work like activity
Engaging with media
Sleeping, dozing
Receiving practical, physical or personal
care
Episodes related to excretion
tion or mockery (Bradford Dementia Group 1997), these
are noted on the data sheet and included in the feedback
sessions. At the same time positive events are recorded if
care staff show particular skills in communications or
crisis management. These also formed part of the feedback
session to balance any negative reaction to personal detrac-
tors identified.
M
N
P
X
X-cretion
Collation of the data was in accordance with the rec-
ommendations set out in the DCM guidelines and included
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Anti oppressive practice
Table 2
Behavior category grid – January
A
B
C
F
K
L
N
P
X
Category
Articulation
Borderline
Cool
Food
Kum & Go
Labour
Nod
physical
x-cretion
Ted
4
6
8
17
18
53
1
24
10
3
68
106
41
32
60
8
19
160
9
17
25
19
15
85
75
18
23
1
2
119
9
4
5
2
6
1
4
1
3
2
Kath
Hatty
John
Alice
Totals
11
50
61
14
14
26
11
Table 3
Behavior category grid – July
A
B
C
F
K
M
N
P
X
Category
Articulation
Borderline
Cool
Food
Kum & Go
Media
Nod
physical
x-retion
Ted
Ben
Hatty
Victor
Alice
Totals
13
9
11
29
28
90
31
28
58
23
47
26
5
21
3
1
56
24
23
27
18
18
1
23
3
35
3
33
4
9
7
5
6
2
4
3
5
3
7
3
4
1
4
3
22
29
187
110
65
58
20
18
total amount of time patients spent in each behavior cat-
egory and the overall well being/ill being score for each
patient (Tables 2, 3, Figs. 3–6).
staff were briefed to allay their fears. Any staff not happy
with the procedure were allowed to opt out of the exer-
cise. In the event nobody did. The staff then obtained per-
mission from either the resident or a relative of the
resident, if the resident were unable to give informed
consent. The ethics of carrying out research on people who
are unable to give informed consent were taken into
account and any resident who objected to being observed
during the research process would immediately be omitted
from the exercise. In the event no objections were made.
Observation of physical care was not made and public
areas only were observed. Bedrooms, bathrooms, etc. were
excluded. The Bradford Dementia Group (1997) guidelines
state
Participants
Five residents, one third of the unit’s population, were
observed initially over two days and a follow up visit was
carried out 6 months later when three of the original resi-
dents plus two others, were observed for a further 2 days.
The observation took place in a villa situated within a
complex of similar units. All residents were diagnozed as
‘suffering’ from dementia.
‘
In fact, very few difficulties have arisen, from an ethical
Procedure
point of view, when dementia care mapping is carried
out in a person-centred way. . . . In itself DCM might be
viewed as a moral instrument that works towards
raising the quality of life of people who have dementia’.
Observers positioned themselves in day areas of the unit
and completed raw data sheets with the BCC and WIB
score, for each of the five residents observed, in every 5
minute time frame. Care staff were involved in the process
initially at a briefing session and after 1 week to discuss
the results. Two mappers were involved to ensure reliabil-
ity of data. Results should be viewed in the light of the
small sample and cannot be said to represent other care
facilities. Clearly further work is necessary to include a
larger sample and further mapping is needed to assess if
trends highlighted by this work are maintained over time.
Results
The results are based on observation of seven patients iden-
tified as Ted, Kath, Hatty, etc. (Tables 2 and 3). The results
will be discussed in relation to the predominance of various
behavior categories for these patients shown in Tables 2
and 3. Their level of ill being and well being will also be
considered and the implications for anti oppressive prac-
tice in this setting discussed in the light of such findings
Ethical considerations
(
Figs 1–3). Personal detractors will also be highlighted
The unit manager and the ward manager’s permission was
obtained before the observation commenced and the ward
when relevant and examples of positive events will also be
discussed when related to the subject matter of the study.
©
2000 Blackwell Science Ltd, Journal of Psychiatric and Mental Health Nursing 7, 59–67
63

G. W. Martin & D. Younger
The behavior category codes discussed are found in (Tables
have to be carefully monitored by the carer. The failure to
hear the voice of the person with dementia, however, that
is communicated, is an important consideration when
looking at routes to empowerment. The person with
dementia may become treated as an ‘object’ which needs
only to be kept clean, tidy and sitting quietly. Consulta-
tion, participation and individualized care are ignored in
an effort to get the job done. At best the carer gets caught
up in making choices and decisions based on assumptions
about what the person with dementia wants or needs
(Chapman 1993).
1–3).
For the purposes of data presentation, only the top nine,
of the 24 categories included in the original category
coding list, have been included. The figures shown repre-
senting 5 min of activity, so, for example Alice spent 1 h
15 min eating and drinking during the January observation
period (Table 2 category ‘F’).
The resident’s well and/or ill being values (WIB value)
are important when assessing the overall value of the
behavior observed. Each 5 minute time frame included an
assessment of the patient’s well or ill being for that behav-
ior category on a scale from + 5 to - 5, and the overall
results for each 12 h period can be shown in graph form
for the three participants who were available for both
observation sessions (Figs. 1, 2 and 3). The WIB score was
recorded along with the BCC so that a complete picture
can be achieved. The two sets of coding being shown sep-
arately and analyzed separately. It is important to note that
if a behavior remained in - 1 for more than half an hour
without interruption then it would drop to - 3 and - 5
after a further half hour. ‘N’ (Sleep) follows a similar rule
but allows for an initial 1.5 h in + 1 before the degenera-
tion occurs.
These graphs give a clear indication that + 1 is the pre-
dominant level of well being. According to the Bradford
Dementia Group (1997) this should equate to ‘coping ade-
quately with present situation; some contact with others;
no signs of ill being observed.’
The levels of well and/or ill being can be linked to behav-
ior demonstrated on the grids (Tables 2, 3) and some idea
of behavior which demonstrates ill being identified. For
example high levels of categories ‘C’ (Socially uninvolved)
and ‘N’ (Sleep) may indicate that attention should be given
to include more stimulating activities in the patients day
which may produce an improved WIB score. On the basis
of this data and the behavior categories identified as sig-
nificant, we can now consider the potential for a culture of
anti oppressive practice.
January observation
If we consider some of the behavior categories in Table 2
we can, perhaps, see this process at work. The highest inci-
dence of observed behavior falls within category ‘C’, ‘being
socially uninvolved or withdrawn’. It could, of course, be
argued that this is predominant because of the level of
dementia demonstrated by the residents, but the coding
system takes account of this and includes category ‘A’,
‘interaction with others, verbally of otherwise’. Even inter-
actions with someone who is not able to communicate fully
can be coded under this category. The low level of such
interactions, particularly with Ted and Kath, who have the
highest level of category ‘C’ (socially withdrawn) and ‘N’
(sleep) may indicate that they are seen not as individuals
with diverse needs but ‘objects’ that have minimal needs
based mainly around physical care. It is not possible to get
a clear picture of the level of physical care, given that
observation took place in public areas only, but from the
data it can be seen that Ted received 45 min of physical
care during the first period of observation the highest
recorded. Ted’s WIB value is fairly evenly spread between
+ 1 and - 1 (Fig. 1 – January) indicating that he may show
signs of well being for a time but, because of the lack
of interaction, this tends to decline to ill being as the day
progresses.
John shows an interesting pattern of behavior. His WIB
value is predominantly + 1 which indicates a reasonable
level of well being but if we consider his behavior cat-
egories (Table 2) it becomes clear that much of this well
being is self generated. Categories ‘F’ (Food) and ‘K’ (Kum
& Go) are the highest recorded and during the observation
it was clear that he enjoyed his meals without involvement
from care staff and appeared to get some satisfaction from
walking up and down the unit’s corridor and round the
day rooms usually alone. He would interact with others
when approached and sat for sometime with another resi-
dent who talked to him. His other main + 1 category was
‘L’ (Labour) when he would move furniture around or rub
the carpet. This was seen as a problem by carers who con-
Discussion of results
According to Goldsmith (1996) people with dementia are
disempowered in two ways. Firstly by the illness itself and
secondly by other people’s reactions to the illness. We are
concerned mainly with the latter in this paper although the
persons cognitive ability is also important. It will be easier
to involve people in decision making if they have some
understanding of the situation they face. This is not to say
that people with poor cognitive function should be
excluded from the process, but different factors such as
nonverbal clues or verbal sounds of ill or well being will
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Anti oppressive practice
tinually replaced the chairs in their original position. One
personal detractor was observed during this process when
a carer called him a ‘pest’ without further interaction
occurring. His behavior was seen as a nuisance rather than
demonstrating a need by John for some form of activity. If
an anti oppressive culture had been in place the need may
have been identified and some stimulation given to John
during the day. It is important to point out that personal
detractors were few and, in the main, minor in nature. The
one described about was the most serious observed.
practical task to that of a possible time for therapeutic
interaction’.
Social interaction which did occur was usually frag-
mented in nature. Positive event recording contains a few
examples of this, just one is considered here by way of
example. It was felt that Alice enjoyed listening to music
and she was placed beside a record player, which remained
on for most of the day. At one point on the second day a
carer asked Alice if she still wanted the music as she was
looking agitated; rocking and mumbling. Alice, who was
unable to communicate verbally, appeared to shake her
head and the carer turner the music off. Alice almost imme-
diately looked more relaxed, stopped rocking and sat back
in her chair. The significance of this observation rests in the
carers interpretation of Alice’s nonverbal clues. The carer
showed empathy for Alice by communicating with her and
assessing her reaction to her environment. As a result Alice
was given some control over her life and her care. Alice’s
WIB value is predominantly + 1 (Fig. 3) owing, largely to
her ability to remain in category ‘B’ (Borderline) without
signs of ill being. This situation could be used by the carers
to provide a more diverse range of activities and social
interaction for Alice. By the time of the second observation
a small television had been placed near Alice and its use
was monitored to ensure that Alice wanted to watch it.
This change is reflected in the higher level of category ‘M’
(Media) in Table 3.
The culture of care at the first observation period
(
(
Table 2) is clearly demonstrated by the high level of ‘B’
Borderline), ‘C’ (Socially withdrawn) and ‘N’ (Sleep) cat-
egories which are unlikely to include input by care staff.
Certain residents were allowed to sit without stimulation
or sleep undisturbed for long periods of time during the
day. The other main category relates to food and drink
demonstrating the importance of this activity and was the
central activity of care staff during the observation period.
Certain other categories showed results of less than 10
units of time, or none at all and they include; engaging in
expressive activity, games, handicraft and exercise, which
may indicate the low priority given to these activities or
worse the low value placed on such activities when caring
for people with dementia.
It should be possible to bring about a measure of
empowerment in all manner of small ways (Goldsmith
1
996). They may include games, exercises or handicrafts
Once the process of change starts, hopefully, it would
encourage further change both during and outside the care
giving routine. It may be these care routines and rituals
which reduce communication with residents (Martin
1998). Change may help to undermine such a culture of
oppressive practice and give people with dementia choices
about day-to-day activities as well as care outcomes.
for those who are able to participate but should always
include verbal and nonverbal interaction even if the
response is limited. These interactions need not happen
independently of care but could become part of the care
process. Given the high score that category ‘F’ (Food)
obtained, this could be one area where anti oppressive
practice could be developed, leading to some small measure
of empowerment by giving residents choices around menu,
where they sit, how long they remain at the table. During
the observation, morning and afternoon drinks were
brought round on a trolley, people were left with their tea
or coffee and then the cups were collected with barely a
word spoken to the residents involved. Could not this
activity be made into an event which included choice of
drinks interaction by grouping residents and talking to
them during the time it takes them to drink their tea.
People who needed feeding could be allowed to sit with
others so that the carer could involve them in a group sit-
uation. During the observation there were several incidents
of ‘positive events’ recorded revolving around feeding,
these could be built on to develop a greater degree of inte-
gration and social involvement. As stated by Littlewood
et al. (1997), ‘all wards caring for older people [should] try
to alter their perception of meal times from that of a busy
July observation
It is, perhaps too big a jump to link small changes to
empowerment but examination of the July results does
show that following the feedback session in January
improvements began to take place. Examination of Table 3
gives the clearest indication of this change. One obvious
example is the lower category ‘C’ (Socially withdrawn) and
the increase in categories ‘A’ (Articulation) and ‘B’ (Bor-
derline), which could indicate that a higher level of com-
munication between care staff and residents was observed.
Categories ‘E’ (Expression), ‘G’ (Games) and ‘M’ (Media)
are much more in evidence as a result of a programme of
morning activities and this has shown improvements in a
number of other areas. If we examine Ted’s graph (Fig 1)
we can see that + 1 value has increased from 49% of the
time to 69%. From Tables 2 and 3 we can see that the time
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2000 Blackwell Science Ltd, Journal of Psychiatric and Mental Health Nursing 7, 59–67
65

G. W. Martin & D. Younger
he is sleeping has dropped from 75 units to 33 units and
category ‘B’ (Borderline) has increased from just 1 unit to
difficult to assess. However, a further mapping completed
the following January demonstrated that the improvements
were maintained at that time. This will form part of an
ongoing study to include larger samples in a variety of care
settings. The DCM process, including the feedback sessions
to the care staff, may have helped to bring about a refo-
cusing of practice from one of mainly physical care to one
which values the broader concept of ‘person centred’ care.
The examples highlighted have served to link this change
of emphasis to the level of communication and choice.
This, it is argued, relates to resident empowerment by
allowing a greater degree of participation in decision
making, even if it means that the resident chooses not to
participate. An understanding by the care staff of the ways
that residents are able to make such choices has to take
into account both verbal and nonverbal means of commu-
nicating. It can never be right to use the excuse of an
oppressive culture of care to justify non participation by
residents. Neither is it right to argue that people with
dementia are unable to become involved in decision
making because of their poor cognitive function alone.
Careful assessment of need, involving the resident, utiliz-
ing such skills as empathy, advocacy and patience, can, if
the result of this study are to be accepted, bring about an
anti oppressive environment which is also, potentially an
empowering one and this exercise could be seen to be the
catalyst which brought about these improvements. Once
the concept of change had been grasped by the care givers
then a paradigm shift can occur in which carers, almost
overnight, begin to see their practice differently (Moyes &
Christie 1998). The important task now is to maintain the
momentum for change by ongoing mapping exercises and
staff education programmes to ensure that change is not
only reinforced but also advanced. Oppressive practice will
then, hopefully, become a thing of the past and empower-
ment of people with dementia enhanced as a result.
31. Some of the improvement may be as a result of the
extra time spent during the lunch period (up from 9 to 24
units). He is no longer fed quickly by the care staff in his
chair in the day room but is now brought to the table, given
special utensils and allowed to feed himself. Even though
he tends to drop food and use his hands, the care staff
monitor his progress and encourage him to use a spoon or
to place food so that he can reach it. When he spilt his
pudding during the observation period, the care staff
remarked that he was having a ‘custard day’, tidied him up
and gave him more to replace the spilt food. On both Ted
and Hatty’s chart – 5 and – 3 no longer appear (Figs. 3, 4
–
July). These were due, in January, to the ‘degeneration
rule’ where behavior which lasts for a given length of time
is classified at a lower level. The improvement in the July
results show that interaction is now more regular and well
being is, as a result enhanced. The three July graphs (Figs.
1–3) make it clear that + 1 remains the predominant WIB
state but to a higher degree. This does not mean that there
is no room for further improvement, but it gives a clear
indication that there have been moves in the right direc-
tion by careers in this care setting. It is significant to note
that no personal detractors were observed during this
second set of observations.
Use of this observation tool and subsequent feedback
session after each period of observation, may have high-
lighted the need to change the culture of care towards a
more person centred approach. The ‘Hawthorne effect’
(Bradford Dementia Group 1997) cannot be ignored
however, but as stated in the DCM manual this can be seen
as a positive effect, ‘the experience may provoke a care
team to discover something of its hidden capabilities’
(Bradford Dementia Group 1997). During the second
period of observation residents were much more involved
in the decision making, being offered a choice at lunch time
or being allowed to opt out of activities if they wished.
These small moves toward autonomy are signs that the
practice is becoming less oppressive and the residents are
empowered despite problems they may have with under-
standing and memory.
References
Beavis D. (1998) Personal detractions – a personal account. The
Journal of Dementia Care 6, 24–25.
Bradford Dementia Group (1997) 7th edn. The DCM Method.
University of Bradford, Bradford.
Brooker D. (1995) Looking at them, looking at me. A review of
observational studies into the quality of institutional care for
elderly people with dementia. Journal of Mental Health 4,
145–156.
Brooker D. & Payne M. (1995) Auditing outcomes of care in in-
patient and day patient settings using Dementia Care Mapping.
Can it be done? PSIGE Newsletter 51, 18–22.
Bytheway B. (1995) Ageism. Open University Press, Buckingham.
Chapman A. (1993) Empowerment. In: Dementia: new skills
for social workers (eds Chapman, A. & Marshall, M.), pp.
110–124. Kingsley, London and Bristol.
Conclusion
It is not possible to arrive at a conclusion which applies to
diverse care settings given the sample size, however, it is
clear from the results that a change of culture is underway
in this care environment. If one compares the results from
the July observation to those obtained in January a number
of differences are evident, giving weight to this conclusion.
To what extent this can be said to be lasting change is more
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© 2000 Blackwell Science Ltd, Journal of Psychiatric and Mental Health Nursing 7, 59–67

Anti oppressive practice
Dalrymple J. & Burke B. (1995) Anti-oppressive practice: social
care and the law. Open University Press, Buckingham.
Marshall M. (1997) The state of art in dementia care. Centre for
policy on ageing, London.
Foucault M. (1980) Two lectures. In: Michel Foucault: Power/
Knowledge, Selected Interviews and Other Writings 1972–77
Martin G. (1997) Changing the culture of care for dying patients.
Professional Nurse 12, 498–500.
(
ed Gordon, C.), pp. 78–108. Harvester Press, London.
Martin G.W. (1998) Ritual action and its effect on the role of the
nurse as advocate. Journal of Advanced Nursing 27, 189–
194.
Moyes M. & Christie H. (1998) Focus on each individual’s
experience and emotions. The Journal of Dementia Care 6,
16–18.
Foucault M. (1984) Nietzsche, genealogy, history. In: The Fou-
cault Reader: an Introduction to Foucault’s Thought (ed Rabin-
now, P.), pp. 76–100. Penguin, Harmondsworth.
Gibson C.H. (1991) A Concept analysis of empowerment. Journal
of Advanced Nursing 16, 354–361.
Gilbert T. (1995) Nursing: empowerment and the problem of
power. Journal of Advanced Nursing 21, 865–871.
Goldsmith M. (1996) Hearing the voice of people with dementia:
opportunities and obstacles. Kingsley, London and Bristol.
Kieffer C. (1984) Citizens empowerment: a developmental per-
spective. Prevention in Human Services 3, 9–36.
Rafferty M. (1997) Mental health and the elderly. In: Mental
health nursing: from first principles to professional practice.
(eds Wright, H. & Giddey, M.), pp.177–190. Stanley Thornes,
Cheltenham.
Mullender A. & Ward D. (1991) Self-directed groupwork: users
take action for empowerment. Whiting and Birch, London.
Thompson N. (1993) Anti-Discriminatory Practice. Macmillan,
Basingstoke and London.
Killick J. (1997) Communication: a matter of life and death of the
mind. The Journal of Dementia Care 5, 14–16.
Kitwood T. (1995) Cultures of care: tradition and change. In: The
New Culture of Dementia Care (eds Kitwood, T. & Benson,
S.), pp. 7–11. Hawker, London.
Kitwood T. (1997) The concept of personhood and its relevance
for a new culture of dementia care. In: Care giving in demen-
tia: research and applications, vol. 2. (eds Miesen, B.M.L. &
Jones, G.M.M.), pp. 3–13. Routledge, London.
Wilkinson A.M. (1995) Dementia care mapping: a pilot study of
its implementation in a psychogeriatric service. International
Journal of Geriatric Psychiatry 8, 1027–1029.
Williams J. & Rees J. (1997) The use of ‘dementia care mapping’
as a method of evaluating care received by patients with demen-
tia – an initiative to improve quality of life. Journal of Advanced
Nursing 25, 316–323.
Littlewood S., Saedi S. & Williams C. (1997) Mealtimes: a missed
opportunity? The Journal of Dementia Care 5, 18–20.
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