Motor Control: the strategies and techniques that teach a person how to move; process, conditions, and rate at which a person learns to move
refers to how the CNS organizes, sequences, & executes movement
OTPs focus on the mechanisms & development of movement
when kids are young, we focus on motor skill acquisition through play
as kids develop & grow older, the focus may shift, but is always focused on occupation & function
Includes:
Coordination
Timing
Sequencing
Bilateral Control
Force Production
Balance
Motor Planning
motor performance is the interaction between all of the systems -- cognitive, musculoskeletal, neurologic, sensory, perceptual, social-emotional -- in addition to the environment & task demends
all of the child's systems interact with one another (holistic view), are adaptable & flexible (nothing is static, everything can change)
task demands & environment are also adaptable & flexible
Cognitive - attention, motivation, & self-efficacy
Musculoskeletal - tone, strength, & posture
Muscle Tone– resting state of the muscle (involuntary)
Hypertonicity = usually limited ROM, reduced fluidity and variety of movement & postural control
Hypotonicity = usually excess ROM, reduced fluidity and variety of movement & postural control
Strength— voluntary recruitment of muscle fibers against gravity
Posture— maintaining upright for reaching, sitting/standing/moving, and all ADLs; THE FOUNDATION OF ALL MOVEMENT
Neuromotor development - reflexes, including equilibrium & protective reactions
Sensory - visual, auditory, vestibular, kinesthesia, proprioception, tactile
Perceptual - making sense of sensory stimuli
Social-emotional - negative emotions impact movement
children with motoric issues move in a way that is inefficient, sequenced wrongly, inflexible, uncoordinated
lack variability, adaptability, & flexibility in their movements for a wide range of movements required to interact with the world
compensatory movements - are the result of motoric dysfunction
present as rigid, impaired, & inflexible
adapt the task/environment & facilitate success
whole-task training
Real-life and relevant training (Some “variability”)
Practice sequences are randomly ordered (“Variability”)
Repetitive
Whole-task focused (“Occupation-focused”)
Positive reinforcement (“Feedback”)
part-task training
Learning to shape the child’s ability to perform a task.
Forward or backward chaining is an example
variability
problem-solving
Allow the child to make errors (or get close to it) and figure it out on his/her own. This helps…
Retention of motor skills
Leads to self-correction
Error-based learning - learning from mistakes
improving child's ability to create the correct adaptive response - learning what they did wrong to learn the correct adaptive response/motor plan
meaning
transfer of learning
Natural context must be included
Can do simulated, but then transition to “real life”
Start simple 🡪 complex
modeling - demonstration
**video modeling - record the movements and watch them back to learn from past experiences
verbal cues
brief, not too many words
emphasize movement
feedback - discuss results & performance
Can discuss the errors and the correct movements
Must occur right after the action/movement occurs
mental practice/imagery
Skill practice
Shorter, more frequent practice is better
Allow for variability
More isn’t always better
Mental practice
Similar to Cog interventions
Can use imagery
Can include role playing, video modeling, or imagining
Cognitive Orientation to Daily Occupational Performance (CO-OP)
Goal, plan, do, check
Problem solving approach to learn skills through use of strategies and guided discovery
First, Help them to discover strategies to function/perform
Second, Teach strategies to help them achieve their objectives
Generalize learning to other environments
Transfer learning to other occupations
Constraint-induced Movement Therapy (CIMT)
Intensive Bimanual Therapy
Cerebral Palsy (CP) = developmental motor disorder, non-progressive, damage to a part of the brain
cause not always indicated
can have prenatal, perinatal, and/or postnatal causes that combine together.
Types of Movement
Spastic - resistant to stretch, increases with quick movement
Dyskinetic - Athetoid, choreoathetoid, and dystonic (usually affects whole body)– abnormal movement of one extremity with unintentional movements of the other when initiating a movement
Athetoid: slow, writing movements along with abrupt jerky movements
Choreoathetosis: constant fluctuations high to low with jerky involuntary movements
Dystonia: twisted postures with movement
Ataxic: Shifts in muscle tone, clumsy, poor coordination and balance
Mixed
Areas of the Body
Monoplegia - 1 limb
Hemiplegia - 1 side of the body - arm & leg
Diplegia - 2 limbs, UB or LB
Paraplegia - 2 LB - rarely used
Triplegia - 3 limbs
Quadriplegia - 4 limbs
Tetraplegia - 4 limbs & head
Diagnoses of CP:
Ex. Spastic monoplegia - spastic movements in 1 limb
Brain tells muscle to inappropriately contract or remain inactive
Children compensate with movement & postures to overcome deficit
Atypical movement patterns lead to difficulties with normal motor skill development
Children end up relying on primitive and automatic reflex movement patterns to move
muscle tone & ROM
muscle tone -
Muscle tone is the resistance to passive stretch. What the general muscle stiffness is AT REST
Has to do with the brain’s innervation of the muscle
can be impacted by emotions and mental state.
Hypertonia - body is ready to move at rest (flexor or extensor)
Hypotonia - body is not ready to move at rest
Common - more flexor in UB with scissoring gait - work on breaking up the patterns & spread out (hippotherapy)
reflex activity
postural instability
fine motor
hand function - weak shoulder, Upper Limb contractures, synergistic movement patterns, inability to isolate finger movement
gross motor
secondary issues
depending on where the brain lesion is…
Cognition
Speech
Vision impairment
Hearing impairment
**Contractures, deformity, skin breakdown!!
Many experience pain, associated seizure d/o, swallowing and GI issues, etc
Co-treatment with other disciplines may be necessary
Adaptive equipment training
AAC, mealtime tools, adaptive materials
has to suit the family & the school
take into consideration the environment, feasibility, learning ability of those involved
Casting, orthotic, & splinting
serial static splints lengthen muscle & correct deformity & reduces spasticity
can build into the "conditions" of a goal/objective
Constraint-induced movement therapy (CIMT)
Bimanual therapy
Therapeutic taping (strapping)
supports weakened muscle, improves circulation, reduces pain, improves joint alignment
inhibits inaccurate movements, facilitating proper movement & supporting joint alignment
PAMs
E-stim, cold, or vibration to increase tone to muscle that needs activation; Heat to relax activated muscles
Positioning/handling
Wheelchairs, standers, activity chairs, bath chairs, side-lyers; seating and mobility equipment, slant-boards, foot boards
Preparatory techniques
slow rocking, rotational movements, stretching and relaxation, warmth 🡪 reduces arousal and tone
fast bouncing and movements, vibration, cold 🡪 increases arousal and tone
Complementary & alternative medicine (CAM)
yoga, massage, guided imagery, myofascial release, meditation (all may require advanced certification)
Gaming, robotics, virtual reality
creates the experience of typical movement
Medical interventions
baclofen pump or botox - reduce tonicity
Spina bifida is a birth defect that occurs when the neural tube, which forms the spine and spinal cord, does not close completely during early development in pregnancy
can lead to a range of symptoms, including incontinence, loss of feeling, and leg paralysis, depending on the severity and location of the defect
refers to a group of more than 30 genetic conditions that lead to muscle weakness and degeneration over time.
are caused by mutations in genes responsible for healthy muscle structure and function.
Duchenne (DMD): Most common form - primary affects boys; genetic mutation causing progressive muscle weakness and loss of muscle mass
typically appearing between ages 2 and 6. It leads to severe muscle weakness and often requires wheelchair use by the teenage years.
Becker (BMD): Milder and progresses more slowly; similar to DMD but with a later onset, appearing from childhood to adulthood
may not require wheelchair until mid-30s or later
a genetic disorder characterized by the loss of motor neurons, leading to progressive muscle weakness and atrophy.
caused by a mutation in the survival motor neuron 1 (SMN1) gene, which is essential for the survival of motor neurons in the spinal cord.
The loss of these neurons results in muscle weakness and atrophy, affecting voluntary muscle movements, including those necessary for breathing, swallowing, and walking.
Progressive muscle weakness, particularly in the trunk and limbs
Difficulty with motor skills, such as crawling or walking
Respiratory problems due to weakened chest muscles
Scoliosis and joint contractures
Difficulty swallowing.