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SCHOLARLY PAPER
of some more complex and recent material. Alter- to disruption of higher level control, and the idea
native classifications are presented by Reed that movements controlled by lower levels of the
(19821, Horak (19911, Abernethy and Swallow nervous system occur in stereotyped patterns
(1992) and Shumway-Cook and Woollacott (1995). (Horak, 1991). These models fail to explain the
experimental finding that some complex functions
For the purposes of this paper motor control
such as the gait cycle are driven from a spinal
theories were initially categorised into one of
level.
two broad groups. Theories in the information
processing category explain motor control in terms The hierarchal models emphasise control of
of information flow in the nervous system of the movement by knowledge accumiilated through
organism. Sensory information flows in from experience (Marteniuk et al, 1988) and by inten-
outside, t o be used and stored, and movement tion (Proteau et a l , 1987) and they assume
commands flow outward; there is also extensive internal structure changes with learning. These
information flow between these two systems. assumptions appear to be held by most therapists,
These theories are based on anatomy and who expect that patients will remember some
physiology and information flow in computers, aspects of a movement practised the previous
and the behaviour of animals and humans in session.
laboratory experiments. In contrast, the action
The Generalised Motor Programme
category includes theories which are less reliant
on storage of information and central represen- The concept of the motor programme was dev-
tation of movements, and place greater emphasis eloped from studies of performances of simple
on the role of the environment in movement motor tasks, to explain how high levels of the
generation. Some of these theories are based on nervous system can store representations of a
the assumption that movements are an emergent large number of movements. A generalised motor
property of the dynamics of the physical system programme (GMP) is a rule for producing a proto-
comprising the organism and its environment. type movement; it can be viewed as a set of
commands that is capable of carrying out move-
The present is a n interesting time to examine ments without the use of feedback. The rule is
motor control theories, because a shift of para- general; values of various parameters have to be
digm may be occurring within the motor control specified for a specific movement t o be produced
field (Abernethy and Swallow, 1992). The infor- (Summers, 1981).
mation processing models of motor control have
dominated the field for the last three decades,
but some interpretations of the experimental For example: think of playing tennis. The sight of
evidence supporting these models are now being the other player lining up a shot which will bring the
questioned. Support for models of motor control ball to your forehand side may activate a GMP for
forehand strokes; but the precise force and timing
based on physical principles is growing rapidly
values may have to be specified further if your
(Gentner, 1987; Heuer, 1988). racquet is to contact the ball.
Information Processing Models
Models of motor control falling within the infor- Evidence for the Use of GMPs
mation processing category may be further
1.One of the strongest pieces of evidence for the
classified as hierarchal or neural network models
(Horak, 1991). existence of GMPs is the motor equivalence
phenomenon. It is argued that for this phenom-
Hierarchal Models enon (the production of a functional movement
such as writing, by different body parts) to exist,
One of the assumptions of models categorised as there must be a common set of instructions for
‘hierarchal’ is that the organisation of the nervous which the body part to be used is a n additional
system is ‘top down’ (Horak, 1991). Arguing that specification.
the parts of the brain of more recent phylogenetic
development are more important, supporters
of this view consider that adaptive control of
An apparent application of the notion of the GMP is
complex movements is performed by the cortex,
seen in therapists’ assumptions that rehearsal of a
and the more automatic control of simpler func- skill using one body part may lead subsequently to
tions occurs at lower levels of the nervous system. more co-ordinated performance of the same skill
This point of view has developed from decades by another part. While it is not known if this effect
of debate over whether the peripheral o r more occurs in brain injured people, therapists sometimes
central parts of the nervous system control move- ask for a required movement to be first performed
ment (Reed, 1982). Clinical implications of this by the opposite limb.
view include the concept of release of reflexes due I
2. It has also been proposed that identification of the poor performance therapists should include
aspects of movement which do not change with the possibility that the patient may no longer
changing task conditions would support the exis- have access to a GMP for the movement. Unfor-
tence of abstract motor programmes coded in such tunately hierarchal models offer no prediction
terms (Schmidt, 1988; Magill, 1989). This would of how development of another GMP should be
be potentially useful in rehabilitation because attempted.
knowledge of the ‘language’in which movement is
Much of the empirical literature describes the
controlled may lead to more efficient design of
improvements in outcomes of motor tasks which
motor retraining programmes. However, exten-
occur with practice as continuous functions
sive experimentation has yielded conflicting
(Newell, 1991), supporting the predictions of
findings. It has been proposed that some findings
hierarchal models of motor control. However,
of invariances in temporal parameters of move-
learning in brain damaged subjects has been
ment across different conditions (eg Shapiro et al,
shown to comprise irregular increments in task
1981) are effects of experimental design rather
outcome rather than smooth progressions (for
than real phenomena (Burgess-Limerick et al,
example: Neilson and McCaughey, 1982; Bate
1992).
and Matyas, 1992). This difference may be
due t o the fact that while the tasks practised by
Producing Novel Movements Using the GMP
the normal subjects were already well learned
One of the main advances made by the concept (Newell et al, 1989), the task performances
of a GMP was in its capacity t o explain production of brain injured subjects may have been at
of novel variations of movements (Summers, a n earlier stage of learning. Alternatively, the
1981). One of the experimental paradigms on irregular progress of brain damaged subjects
which this model is based was pointing to a small may indicate that their learning in rehabilita-
target. Using this task as a n example, such a tion does not occur in the manner predicted
novel variation could be produced by setting the by hierarchal models of motor control.
target a different distance from the subject. Thus,
if you have a GMP for the task of touching a call-
button, then you can touch such a button 35 cm in Schema Theory
front of you even if none of the call buttons you Schema theory (Schmidt, 1975),while developed
ever previously pressed were exactly that distance primarily t o describe motor learning, has many
away. This type of novelty, the scaling of a pre- features characteristic of hierarchal theories of
existing movement pattern, is the only type of motor control. The model states that a GMP initi-
new movement which can be explained by the ates a movement, and that feedback from the
concept of a GMP. movement is compared with a generalised sensory
representation to allow corrections and learning.
Without this assumption a therapist might
consider it necessary to guide a brain injured Learning with Schema Theory
patient through practice of every variation of
every task he or she may ever need to perform. Unlike earlier models, schema theory predicts
that variability in task conditions will enhance
However, the GMP concept cannot explain the learning. That is, the GMP will become more
development of new movement forms (that is accurate if variations on the movement are
acquisition of new GMPs). performed, rather as the predictions of a math-
ematical relationship become more reliable
Consider the first time you did a handstand. Did if more points are added t o the data set. This
standing on your hands require a new GMP? If it did, prediction has been supported in a study of
then your performance could not be easily explained stroke patients learning a pursuit tracking task
by this model. (Bate et al, 1992).
[There is another possibility:a GMP for that task could This model also predicts that we do not learn from
have existed in your central nervous system, geneti-
passive movements. Assuming this to be true,
cally coded, never to be activated until that day.
Perhaps you had to practise to find the appropriate
therapists are challenged to create situations in
values for the timing and force parameters of this which action is demanded from a paralysed limb.
pre-existing, never-used GMP.] Finally, schema theory predicts that learning
requires active processing of feedback; in infor-
This limitation of hierarchal control theory mation theory terms this means it requires
offers insight in relation to the management of attention. Consonant with this model of learning,
brain injured patients who are unable to perform movement rehabilitation places heavy emphasis
a particular task, or who perform it very poorly. on patients’ attention t o feedback (Carr et a l ,
In considering the many factors contributing t o 1987; Bobath, 1990).
in an arena commonly known as the ‘perceptuo- ated in real time from interaction between the
motor workspace (perceptuo-motor field)’ (Newell organism and the environment, predict that novel
et al, 1989). movements would arise if the environment, the
organism, or their interaction was altered. Thus,
Field-orientedTheory of Perception some action theories predict t h a t people could
An understanding of the integral nature of the effectively handle a joystick if their environment
relationship between perception and movement suddenly included an unconscious pilot, even if
emphasised in action theories can be gained by they had not done so before.
interpreting actions in terms of Gibson’s (1979)
field-oriented theory of perception. The environment is given more importance in this
model than in traditional forms of rehabilitation. The
This theory emphasises the complex role of the implication for rehabilitation following brain injury is
optic flow field in movement production. The optic that therapists could change the environment in such
flow field is the pattern of stimuli on the retina a way that the interaction of the patient with the
produced by the interaction between the organism environment generates the required movement.
and the environment. This optic flow field is In addition to changing the patients’ cognitive envir-
onment by giving specific instructions, or altering their
controlled by movement, and it also provides
biomechanical environment by applying a mod-
information for both perceiving and action.
ality such as ultrasound or stretching, their external
environment could be modified so that it facilitates
Imagine a horse running fast on an open plain. As it better performance.
runs, the long grass in front of it appears to the horse
to move closer, and then to flow past on each side. Action theories such as the field-oriented theory
The horse sees the grass stems on either side of perception (Gibson, 1979), which emphasise the
moving backwards very fast, and the mountains role of perception in motor control, do not clearly
moving more slowly. The horse swerves in the direc- address the issue of learning. It is interesting
tion of a tree, and the tree appears to it to move in the to speculate what effects movement training
opposite direction, towards the centre of the field of may have in terms of this model. Presumably
view, and to move closer. In this example the optic finer discrimination of sensory stimuli, and finer
flow field has provided information about speed and
tuning of motor mechanisms, could lead t o gener-
direction of running. Also, change in the speed and
direction of running caused concomitant change in
ation of more finely co-ordinated movements.
the position and movement of the stimuli impinging However, the way in which such increases in
on the retina. That is, movement changed the optic capacity of the organism would occur is not spec-
flow field, and the optic flow field provided information ified in many action models.
controlling both perception and action.
Dynamic Emphasis in Action Theories
Consider that you are landing an aeroplane in a
computer simulation. You hold a joystick, and are Emphasising the importance of interaction
watching a moving graphical display of the view from between the organism and the environment in
the pilot’s seat. This includes ground features such movement production Kugler et al (1980) eluci-
as bushes and grass around the landing strip, the dated a constraint perspective of motor control
edges of the landing strip, and lines painted across which was based on the work of Feldman (1986),
the strip every 20 metres. You have no other infor- Polit and Bizzi (1978) and Bernstein (1967). This
mation. You watch the relative positions and changes model explains the use of constraints in move-
in position of these visual stimuli and use this infor- ment production in terms of physics and biology;
mation to control the height, pitch, yaw and roll of the we obey the laws of mechanics, acting like springs
plane through the joystick. That is, the optic flow field and pendulums and more complex systems in
changed the movement of your arm, and hence the
interacting with the environment. In contrast to
aeroplane. In this example also, while movement
changed the optic flow field, the optic flow field neural network theories, which support a large
provided information controlling both perception amount of information processing occurring
and action. in parallel systems, one of the effects of control
based on dynamic principles is minimisation
of the computational load on the nervous system.
Following publication of Gibson’s theory, it was For each task some of the dynamic properties
proposed that the organising role of optic flow in of the human action system are assembled,
movement production may be extended to other temporarily, into a ‘low-dimensionaldeterministic
modalities (Newell et al, 1989). That is, in the machine that is used to achieve the goals’ of the
language of action models, not only the visuo- task (Bingham, 1988, page 240). The term ‘low-
motor field, but more broadly, the perceptuo- dimensional’ here refers to the small number of
motor field, may organise movement. variables which would have t o be controlled by
Action theories, in which movements are gener- computational processes.
further discussion by therapists. Some of the Heuer, H (1988). 'Testing the invariance of relative timing:
Comment on Gentner (1987). Psychological Review, 95,
predictions of the theories reviewed are empiri- 552-557.
cally testable within the rehabilitation paradigm,
Hirayama, M, Jordan, M I and Kawato, M (1993). 'The cascade
offering opportunity for sound research within neural network model and a speed-accuracy trade-off of arm
our field. movement', Journal of Motor Behavior, 25, 3, 162-1 74.
Hogan, N (1984). 'An organising principle for a class of volun-
tary movements', Journal of Neuroscience, 4, 2745-54.
Author and Address for Correspondence Hogan, N, Bizzi, E, Mussa-lvaldi, F and Flash, T (1987). 'Control-
Patricia Bate MAppSci BAppSc(Phty) MAPA is a senior lecturer ling multijoint motor behaviour', Exercise and Sports Science
in the School of Physiotherapy, Faculty of Health Sciences, Reviews, 15, 153-190.
La Trobe University, Plenty Road, Bundoora, Victoria, Australia.
Horak, F (1 991). 'Assumptions underlying motor control for
neurologic rehabilitation', in: Contemporary Management
This article was received on October 10, 1996, and accepted on
of Motor Control Problems, Proceedings, 11 Step Conference,
December 2, 1996.
Foundation for Physical Therapy, New York.
References Kugler, A N, Kelso, J A S and Turvey, M T (1980). 'On the
Abbs, J H and Cole, K J (1978). 'Neural mechanisms of motor concept of co-ordinative structures as dissipative structures.
equivalence and goal achievement' in: Wise, S P (ed) Higher 1: Theoretical lines of convergence' in: Stelmach, G E and
Brain Functions, Wiley, USA. Requin, J (eds) Tutorials in Motor Behaviour, Elsevier Science,
Amsterdam.
Abbs, J H, Gracco, V L and Cole, K J (1984). 'Control of multi-
movement co-ordination: Sensorimotor mechanisms in speech Magill, R A (1989). Motor Learning: Concepts and applications,
motor programming', Journal of Motor Behavior, 16, 195-231. W C Brown, Indianapolis, 3rd edn.
Abernethy, B and Swallow, A (1992). 'The rise and fall of domi- Marteniuk, R G, McKenzie, C L and Leavitt, J L (1988). 'Repre-
nant paradigms in motor behaviour research' in: Summers, J J sentational physical accounts of motor control and learning:
(ed) Approaches to the Study of Motor Control and Learning, Can they account for the data?' in: Colley, A M and Beech, J R
Elsevier Science, Amsterdam, pages 343-384. (eds) Cognition and Skilled Behaviour, Elsevier, Amsterdam.
Bate, P J and Matyas, T M (1992). 'Negative transfer of training Neilsen, P D and McCaughey, P (1982). 'Self regulation of spasm
following brief practice of elbow tracking movements with and spasticity in cerebral palsy', Journal of Neurology, Neuro-
electromyographic feedback from spastic antagonists', surgery and Psychiatry, 45, 320-330.
Archives of Physical Medicine and Rehabilitation, 73, 1050-58. Newell, K M, Kughler, P N, Van Emmerik, R A E and McDonald,
Bate, P J, Matyas, T and Rogers, D R (1992). 'Movement rehab- P V (1989). 'Search strategies and the acquisition of co-ordina-
ilitation following brain damage: Transfer of training after tion', in: Wallace, S A (ed) Perspectives on the Co-ordination of
consultant or variable practice,' presented at Allied Health Movement, Elsevier, Amsterdam.
Research Seminar, Austin Hospital, Melbourne. Newell, K (1991). 'Motor skill acquisition', Annual Review of
Bernstein, N A (1967). The Co-ordination and Regulation of Psychology, 42,213-237.
Movement', Pergamon Press, Sydney. Polit, A and Bizzi, E (1978). 'Processes controlling arm move-
Bingham, G P (1988). 'Task specific devices and the perceptual ments in monkeys', Science, 201, September 29, 1235-37.
bottleneck', Human Movement Science, 7,225-264. Proteau, L, Marteniuk, R G, Gerouard, Y and Dugas, C (1987).
Bobath, B (1990). Adult Hemiplegia: Evaluation and treatment, 'On the type of information used to control aiming movements
Heinemann, London, 3rd edn. after moderate and extensive training', Canadian Journal of
PSyCholOgy, 6,181-199.
Burgess-Limerick, R, Neal, R J and Abernethy, B (1992). 'Against
relatiye timing invariance in movement kinematics', Quarterly Reed, E S (1982). 'An outline of a theory of action systems,
Journal of Experimental Psychology, 44A, 4k, 705-722. Journal of Motor Behavior, 14, 2, 98-134.
Carr, J H, Shepherd, R S , Gordon, J, Gentile, A M and Held, J M Schmidt, R A (1975). 'A schema theory of discrete motor skill
(1987). Movement Science: Foundations for physical therapy learning', Psychological Review, 82, 225-260.
in rehabilitation, Aspen, Maryland. Schmidt, R A (1988). Motor Control and Learning: A behavioral
Carnahan, H and Marteniuk, R G (1991). 'The temporal organi- emphasis, Human Kinetics, Illinois, 2nd edn.
sation of hand, eye and head movements during reaching Shapiro, D C, Zernicke, R F, Gregor, R J and Diestal, J D (1981).
and pointing', Journal of Motor Behavior, 23, 2, 109-1 19. 'Evidence of generalised motor programmes using gait pattern
Cole, K J and Abbs, J H (1986). 'Kinematic and electromyo- analysis', Journal of Motor Behavior, 13, 33-47.
graphic responses to perturbation of a rapid grasp', Journal of Shumway-Cook, A and Woollacott, M (1995). Motor Control:
Neurophysiology, 57, 1498-1 510. Theory and practical application, Williams and Wilkins, Baltimore.
Cruse, H, Bruwer, M and Dean, J (1993). 'Control of three- and Soechting, J F (1982). 'Does position sense at the elbow reflect
four-joint arm movement: Strategies for a manipulator with redun- a sense of joint angle or one of limb orientation?' Brain Research,
dant degrees of freedom', Journal of Motor B e / ~ v i o r , 248, 393.
25,3, 131-1 39.
Soechting, J F (1989). 'Elements of co-ordinated arm movements
Feldman, A G (1986). 'Once more upon the equilibrium-point in three-dimensional space' in: Wallace S A, Perspectives on the
hypothesis (lambda model) for motor control', Journal of Motor Co-ordination of Movemenf, Elsevier, Amsterdam.
Behavior, 18, 17-54.
Summers, J J (1981). 'Motor programs' in: Holding, D (ed)
Feldenkrais, M (1980). Awareness Through Movement, Penguin, Human Skills, John Wiley and Sons, New York.
Middlesex.
Summers, J J (1992). 'Movement behaviour: A field in crisis?'
Flash, T and Hogan, N (1982). 'Evidence for an optimisation in: Summers, J J (ed) Approaches to the Study of Motor Control
strategy in arm trajectory formation', Society of Neuroscience and Learning, Elsevier, Amsterdam.
Abstracts, 8, 282. Turvey, M T (1990). 'Co-ordination', American Psychologist,
Gentner, D R (1987). 'Timing of skilled motor performance: Tests August, 938-953.
of the proportional duration hypothesis', Psychological Review, Uno, Y, Suzuki, R and Kawato, M (1989)..'Minimum muscle
94,255-276. tension change model which reproduces a human arm move-
Gibson, J J (1979). The Ecological Approach to Visual Percep- ment', Proceedings of the Fourth Symposium on Biological and
tion, Houghton Mifflin, Boston. Physical Engineering, Fukuoka, Japan, 299-302.