L1 - Principles of Motor Learning Flashcards

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1
Q

Why is motor control important?

A

It affects all areas of life, and therefore can easily reduce quality of life if impaired.

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2
Q

Neurological conditions can affect the ______, ______, ______ and ______ of movement.

A

Neurological conditions can affect the speed, fluency, quality and ease of movement.

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3
Q

What does optimal control theory assume?

A

You will optimise whatever aspect of movement you think is important, at the peril of remaining aspects of movement.

E.g. if speed is optimised, you will forget about fluency, ease and quality.

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4
Q

What did Higgins (1991) suggest about the expectation of therapists?

A

Therapists should not expect that one way of performing a task is the most effective and efficient for all patients.

–> it doesn’t matter how people do it, just that it gets done.

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5
Q

What are the two possible ways to focus therapy?

A

Either normalising patients by countering the deficiencies that drive their movement impairments (e.g. whether strength, flexibility, etc), or by ensuring they can carry out a particular task (function).

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6
Q

Why is voluntary movement vulnerable to impairments?

A

Different areas are highly integrated to perform voluntary movements. Therefore, an impairment in one area could influence and impair the whole process.

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7
Q

What is the goal of the brain in terms of action selection, according to the affordance model?

A

The most rewarding and least effortful task.

Multiple actions are initially specified and then gradually eliminated in a competition for overt execution, as more information accumulates.

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8
Q

Which area of the brain is responsible for action selection?

A

Basal ganglia

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9
Q

In PD patients, what are the features of their movements and what does this suggest?

A

Movements are slow, but remain accurate. Sign that there’s a problem with selection, and the integration and execution of movement is ok, it’s more high level processes that are impaired.

Fellows et al., (1998) - PD patients took longer to normalise grip forces and complete a lift, compared to controls. Suggested reduced effectiveness at the sensorimotor processing stage in PD (and perhaps communication between the BG and SMA, specifically abnormal signals from the BG).

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10
Q

What does SMA stand for?

A

Supplementary motor area

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11
Q

What does the SMA do?

A

Planning and executing complex actions.

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12
Q

What do lesions to the SMA lead to?

A

Difficulties in completing sequential movements (and complex actions), i.e. picking up a cup will be challenging as it involves several processes - intention to pick it up, reaching the cup with the hand, grasping the cup, lifting it and then retracting the arm back.

Completing any one component of this action would be fine, e.g. just grasping the cup - its the combination and integration of all components that would be a problem.

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13
Q

Damage to the cerebellum typically produces what?

A

Inaccurate movements

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14
Q

What is the main role of the cerebellum?

A

Prediction

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15
Q

What does PMD and PMV stand for?

A

Premotor area - dorsal and ventral

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16
Q

What is the role of the premotor area?

A

Preparation of movement, response to external cues (e.g. traffic lights), grasp planning and action understanding.

17
Q

What does the PPC stand for?

A

Posterior parietal cortex

18
Q

What is the role of the PPC?

A

It estimates body, head, eye and arm positions in relation to the environment by integrating motor and sensory signals. It then sends this information to pre-motor areas to allow successful movement planning and execution.

19
Q

Where is the PPC located?

A

Between the visual and motor structures in the brain

20
Q

Which area controls the programming of movements?

A

Primary motor cortex (M1)

21
Q

What is M1 important for, and how does this relate to the organisation of its cortex?

A

Important for control of skillful movement, especially of hands, mouth and face.

Contralateral body represented spatially across the cortex.

The hands, mouth and face have the most representation in the cortex (as they are the most sensitive areas) and they therefore are controlled most by M1.

22
Q

What, generally, do efferent fibres do?

A

Carry impulses away from the CNS

23
Q

What, generally, do afferent fibres do?

A

Carry impulses to the CNS

24
Q

Brodmann area 3a and 3b receive inputs from where?

A

Receives sensory inputs from the thalamus.

25
Q

Where does Brodmann area 1 receive inputs from?

A

Mainly from Broadmann area 3b, and defines texture

26
Q

Where does Brodmann area 2 receive input from?

A

Mainly from Broadmann area 3b and defines shape and size

27
Q

What are upper motor neuron syndromes?

A

Syndromes characterised by damage above the level of motor neurons. E.g. Stroke, tumours - affect cortical areas.

28
Q

What are lower motor neuron syndromes?

A

Syndromes characterised by damage to alpha motor neurons, affecting either afferent or efferent information to muscles. E.g. Progressive muscular atrophy, bulbar palsy

29
Q

What are extrapyramidal disorders?

A

Disorders characterised by damage to the basal ganglia.

e.g. Parkinson’s, Huntington’s

30
Q

What are cerebellum disorders?

A

Disorders characterised by damage to the cerebellum.

e.g. cerebellar ataxia, etc.

31
Q

What did Haswell et al., (2009) find and conclude?

A

While controlling a novel tool, autistic children formed greater than normal associations between their self-generated motor commands and proprioceptive feedback (rather than external feedback). The strength of this association correlated with the individual’s social function and imitation impairments.

The neurons representing the internal model are located in M1, and proprioception takes place in the somatosensory cortex. Use of external (e.g. visual/imitation) cues takes place in PMA/PPC, which is further away from M1 than the sensorimotor cortex.

Suggests that, in autism, an overgrowth of short-range connections means they learn more through intrinsic coordinates than extrinsic coordinates, and that this could underlie the social deficits in ASDs.