IC15 Staudt 2
IC15 Staudt 2
Score Sheet
Date: _______________ Patient’s Name: __________________________________ DOB: __________________ GMFCS level: _____
Left Right
Grade Hip Knee Ankle STJ Toes Hip Knee Ankle STJ Toes
Normal (2 points)
Impaired (1 point)
Unable (0 points)
Total Limb Score L= R=
Resisted Synergy
knee extension with resisted limb extension
dorsiflexion with resisted limb flexion
Descriptors
hip flexion contracture
adductor contracture or spasticity
knee flexion contracture
hamstring tightness
plantar flexion contracture
plantar flexor spasticity
inverts or everts, not pure dorsiflexion
primarily moves toes
mirrors motion on opposite limb
motion slower than 3 second verbal count
moves one direction only (note motion achieved)
movement of other joints
motion < 50% of available ROM
____________________________________________________________________________________________
____________________________________________________________________________________________
____________________________________________________________________________________________
________________________________
Examiner
Version 2.3, Copyright 2009 – University of California Los Angeles/Orthopaedic Hospital Center for Cerebral Palsy
SCALE: Directions for administration
The patient must be able to follow simple motor commands. To test this ability, ask the patient to move his or her least affected body part.
Before asking the patient to perform each joint test, passively move the joint to assess ROM. To assure understanding, demonstrate the
movement sequence while supporting the limb. The language in the instructions to the patient is suggested and may be modified as
needed to elicit optimum performance for individual patients. To guide patients in the desired speed of movement, provide a verbal
three-second count during the task. Multiple attempts are allowed and feedback to improve performance is acceptable.
General instructions to patient – “I am going to ask you to move in a certain way. Move the way I ask you to move. Try not to move any
other part of your body. If you have any questions or you don’t understand what I am asking you to do, please tell me.”
Hip
Position – Side lying with the hip and knee fully extended. Support the limb medially at the knee and ankle. For stability, you may flex the
lower untested limb. The tested motion is hip flexion while keeping the knee extended. Assess hip flexion ROM with the knee extended, as
it may be limited by hamstring tightness. If the patient has difficulty with this task because of hamstring tightness, then ask him or her to
extend, flex then extend the hip while keeping the knee flexed 90o. Evaluate hip extension ROM to assure an adequate arc of motion to
assess performance of the task.
Instructions to patient – Ask the patient to flex, extend then flex the hip while keeping the knee extended. For example: “Move your leg
forward, back then forward again while keeping your knee straight. I will take you through the motion first, and then I’d like you to do it
yourself.”
Knee
Position – The remaining tests are done in sitting with legs over the edge of the exam table. During the remaining tests you may allow the
patient to lean back on his or her hands so the trunk is approximately 20o from vertical to compensate for hamstring tightness.
Instructions – Ask the patient to extend, flex then extend the knee while keeping the hip flexed. For example: “Straighten your knee as
much as you can, then bend it and straighten again. Try to do this without leaning further back or moving your other leg. I will take you
through the motion first, and then I’d like you to do it yourself.”
Limb Extension Synergy – If quadriceps weakness is suspected, limb extension synergy may be assessed. Allow the patient to lean back
on his or her hands or be supported so the trunk is approximately 45o from vertical. Position the limb in hip and knee flexion with ankle
dorsiflexion. Ask the patient to push against your hand, extending the knee and plantar flexing the foot and toes. Resist at the metatarsal
heads and compare knee extension excursion to the amount achieved during the knee selective voluntary motor control test.
Ankle
Position – Sitting, as in the knee extension test. The knee is extended and the examiner supports the calf. Assess passive ankle
dorsiflexion ROM with the knee extended. The knee may be flexed to approximately 20o if needed to accommodate hamstring and/or
gastrocnemius tightness.
Instructions to patient – Ask patient to dorsiflex, plantar flex then dorsiflex the ankle while maintaining knee extension. For example:
“Keeping your knee straight while I support your leg, move your foot up, down then up again. I will take you through the motion first, then
I’d like you to do it yourself.”
Limb Flexion Synergy (Confusion Test) – If dorsiflexor muscle weakness is suspected, limb flexion synergy may be assessed. Ask the
patient to flex the hip while keeping the knee flexed. Resist hip flexion at the distal thigh. Compare dorsiflexion excursion to the amount
achieved during the ankle selective voluntary motor control test.
Foot/Subtalar Joint
Position – Sitting, as in the knee and ankle tests. The calf is supported.
Instructions to patient – Ask patient to invert, evert then invert while maintaining knee extension. For example: “Move your ankle in, then
out then in again while I support your leg. I will take you through the motion first, then I’d like you to do it yourself.”
Toes
Position – Sitting, as in the ankle test. The heel is supported.
Instructions to patient – Ask patient to flex, extend then flex toes without moving ankle or knee. For example: “Curl all your toes down,
then up then down again while I support your leg. I will take you through the motion first, then I’d like you to do it yourself.”
Version 2.3, Copyright 2009 – University of California Los Angeles/Orthopaedic Hospital Center for Cerebral Palsy
SCALE: Selective Control Assessment of the Lower Extremity
Instructions for Grading
Each joint is scored either 2,1 or 0 points. These are summed for a Total Limb Score. The number of points for each grade is in parentheses. For each
joint, check the joint score and all applicable descriptors on the SCALE Score Sheet.
Hip
Normal (2) Flexes, extends then flexes again. During flexion, movement occurs without knee flexion, within a three-second verbal count and
without mirror movement (the same movement on the contralateral limb). If alternate hip extension test is used, extends, flexes then
extends again. During extension, movement occurs without knee extension, within a three-second verbal count and without mirror
movement.
Impaired (1) One or more of the following occur: extends or flexes < 50% of available range of motion in the test position, performs task slower
than three-second verbal count, exhibits mirror movements, movement occurs in only one direction or motion at untested joint
occurs.
Unable (0) Does not flex or extend hip or does so only with simultaneous knee movement.
Knee
Normal (2) Extends, flexes and extends again. Movement occurs within three-second verbal count, without motion of the trunk or other joints
and without mirror movement. A Normal grade may be given if the knee extends > 50% of available range of motion in the test
position.
Impaired (1) One or more of the following occur: extends < 50% of available range of motion, performs task slower than three-second verbal
count, exhibits mirror movements, movement occurs in only one direction or motion at untested joint occurs.
Unable (0) Does not extend or only extends with simultaneous hip or ankle movement.
Ankle
Normal (2) Dorsiflexes, plantar flexes and dorsiflexes again. Movement occurs within a three-second verbal count, without motion at other joints
and without mirror movement. At least 15o of ankle motion in the sagittal plane must be observed.
Impaired (1) One or more of the following occur: dorsiflexes < 50% of available passive range of motion in the test position or active range during
Limb Flexion Synergy, performs task slower than three-second verbal count, exhibits mirror movements, movement occurs in only
one direction or motion at untested joint occurs. An “Impaired” grade is given if the motion is accompanied by toe extension or ankle
inversion.
Unable (0) Does not dorsiflex or only dorsiflexes with hip and knee flexion.
Foot/Subtalar Joint
Normal (2) Inverts, everts and inverts again. Movement occurs within a three-second verbal count, without motion at other joints and without
mirror movement. Active eversion must occur.
Impaired (1) One or more of the following occur: inverts or everts < 50% of available range of motion, performs task slower than three-second
verbal count, exhibits mirror movements, movement occurs in only one direction or motion at untested joint occurs.
Unable (0) Does not invert or evert or movement occurs only in synergy pattern. May dorsiflex, plantar flex or not move ankle at all.
Toes
Normal (2) Flexes, extends and flexes again. Movement occurs within a three- second verbal count, without motion at other joints and without
mirror movement. Motion should occur at all five toes.
Impaired (1) One or more of the following occur: flexes or extends < 50% of available range of motion, performs task slower than three- second
verbal count, exhibits mirror movements, movement occurs in only one direction or motion at untested joint occurs.
Unable (0) Does not flex or extend toes.
Version 2.3, Copyright 2009 – University of California Los Angeles/Orthopaedic Hospital Center for Cerebral Palsy
DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY ORIGINAL ARTICLE
1 Department of Orthopaedic Surgery, UCLA ⁄ Orthopaedic Hospital Center for Cerebral Palsy and Tarjan Center, David Geffen School of Medicine at UCLA, Los Angeles,
CA, USA. 2 Department of Orthopaedic Surgery, UCLA ⁄ Orthopaedic Hospital Center for Cerebral Palsy, and Department of Pediatrics, David Geffen School of Medicine
at UCLA, Los Angeles, CA, USA.
Correspondence to Dr Eileen G Fowler UCLA ⁄ Orthopaedic Hospital Center for Cerebral Palsy, 22-64 Rehabilitation Center, 1000 Veteran Avenue, Los Angeles, CA
90095-1795, USA. E-mail: efowler@mednet.ucla.edu
PUBLICATION DATA Normal selective voluntary motor control (SVMC) can be defined as the ability to
Accepted for publication 9th September 2008. perform isolated joint movement without using mass flexor ⁄ extensor patterns
Published online 12th February 2009. or undesired movement at other joints, such as mirroring. SVMC is an important
determinant of function, yet a valid, reliable assessment tool is lacking. The
LIST OF ABBREVIATIONS
Selective Control Assessment of the Lower Extremity (SCALE) is a clinical tool
CST Corticospinal tract
developed to quantify SVMC in patients with cerebral palsy (CP). This paper
ICC Intraclass correlation coefficient
describes the development, utility, validation, and interrater reliability of SCALE.
PWM Periventricular white matter
SCALESelective Control Assessment of the
Content validity was based on review by 14 experienced clinicians. Mean agree-
Lower Extremity ment was 91.9% (range 71.4–100%) for statements about content, administra-
SVMC Selective voluntary motor control tion, and grading. SCALE scores were compared with Gross Motor Function
Classification System Expanded and Revised (GMFCS-ER) levels for 51 partici-
ACKNOWLEDGMENTS pants with spastic diplegic, hemiplegic, and quadriplegic CP (GMFCS levels I
We acknowledge statistical consultation from – IV, 21 males, 30 females; mean age 11y 11mo [SD 4y 9mo]; range 5–23y).
Jeffrey Gornbein, and contributions from Beth Construct validity was supported by significant inverse correlation (Spearman’s
Trevino, Sarah Copeland, and Evan Goldberg. r=-0.83, p<0.001) between SCALE scores and GMFCS levels. Six clinicians rated
We thank all of the clinical experts and the 20 participants with spastic CP (seven males, 13 females, mean age 12y 3mo [SD
volunteer patients and their families for their
5y 5mo], range 7–23y) using SCALE. A high level of interrater reliability was
participation, and the Lena Longo Foundation
demonstrated by intraclass correlation coefficients ranging from 0.88 to 0.91
and the Brianna Fund for financial support.
(p<0.001).
Children with spastic cerebral palsy (CP) exhibit multiple or posture.’5 The term ‘selective voluntary motor control’
impairments that contribute to functional motor deficits. (SVMC) differentiates the deliberate performance of iso-
Although spasticity and contractures may be more obvious lated movements upon request from habitual selective
impairments, underlying deficits in selective motor control muscle activation during functional tasks, such as walking.
can negatively affect function to a greater degree.1,2 Assess- Voluntary movement is produced through the cortico-
ment of selective motor control in lower extremities in spinal tracts (CSTs), which control both directionality and
patients with CP has received little attention, despite force production.6 Damage to the CSTs interferes with
growing support for it as a predictive factor of functional the force, speed, timing, and pattern of volitional move-
ability.1–4 ments.7 Injury to CSTs within the periventricular white
Selective motor control has been defined as ‘... the matter (PWM) has been correlated with motor disability
ability to isolate the activation of muscles in a selected in CP.8 Damage to PWM was the most common finding
pattern in response to demands of a voluntary movement in brain scans of children with spastic diplegia, and was
pattern at two or more joints.23,24 If the patient does not 1. The order of test administration is appropriate.
2. The inclusion of a resisted flexor synergy pattern is needed or
initiate the requested movement sequence, extensor and
useful.
flexor synergy patterns may be elicited using manual resis-
3. The inclusion of a resisted extensor synergy pattern is needed
tance to verify muscle force-generating capacity. A
or useful.
SCALE score for each limb is obtained by summing the
4. The Total Limb Score is needed or useful.
points assigned to each joint for a maximum of 10 points 5. The Total Limb Score categories are appropriately distributed.
per limb.
Totala (n=20) Team A (n=10) Team B (n=12) Table III: Characteristics of participants for construct validity (n=51)
Number of responses
2
14 2 ability to follow simple motor commands is necessary, it is
2
12 3 2 least suitable for patients under 4 years of age and those
4
10 2 with severe motor and intellectual impairments (GMFCS
8 2 2 V). Although scoring may not be possible for these
6 patients, SVMC can be described based on observations of
2
4 4
spontaneous movements. In our experience, patients classi-
2 2
3
fied at GMFCS level V were more likely to have dyskine-
0
I II III IV sia, which SCALE was not designed to address. Although
GMFCS-ER designed for use in CP, SCALE may be useful for assess-
ment of patients with other types of neurological involve-
Figure 1: Relationship between total Selective Control Assessment
ment such as hereditary spastic paraparesis, traumatic brain
of the Lower Extremity (SCALE) scores (sum of left and right) and injury, multiple sclerosis, or stroke.
Gross Motor Function Classification System - Expanded and Revised
version (GMFCS-ER) levels (n=51). Numerals to the right of symbols CONCLUSION
indicate the number of participants who share the same data point. Evidence for construct and content validity is presented
Spearman's rank correlation coefficient = –0.83, p<0.001. here as the first step in the validation of SCALE. Recent
work has shown that SCALE scores are correlated with
REFERENCES European Cerebral Palsy Study. JAMA ening for children with cerebral palsy
1. Ostensjo S, Carlberg EB, Vollestad NK. 2006; 296: 1602–08. (PEDALS)—a randomized controlled trial
Motor impairments in young children 10. Tedroff K, Knutson LM, Soderberg GL. protocol for a stationary cycling interven-
with cerebral palsy: relationship to gross Synergistic muscle activation during maxi- tion. BMC Pediatr 2007; published online
motor function and everyday activities. mum voluntary contractions in children (DOI: 10.1080/14038190801999620).
Dev Med Child Neurol 2004; 46: 580–89. with and without spastic cerebral palsy. 19. Trost J. Physical assessment and observa-
2. Voorman JM, Dallmeijer AJ, Knol DL, Dev Med Child Neurol 2006; 48: 789–96. tional gait analysis. In: Gage JR, editor.
Lankhorst GJ, Becher JG. Prospective 11. Bhattacharya A, Lahiri A. Mirror move- The treatment of gait problems in cerebral
longitudinal study of gross motor function ment in clinical practice. J Indian Acad palsy. Clinics in Developmental Medicine
in children with cerebral palsy. Arch Phys Clin Med 2002; 3: 177–81. No. 164–5. London: Mac Keith Press,
Med Rehabil 2007; 88: 871–76. 12. Perry J. Determinants of muscle function 2004: 71–89.
3. Staudt LA, Peacock W. Selective posterior in the spastic lower extremity. Clin Orthop 20. Löwing K, Carlberg EB. Reliability of the
rhizotomy for the treatment of spastic Relat Res 1993; 288: 10–26. Selective Motor Control Scale in children
cerebral palsy. Pediatr Phys Ther 1989; 13. Fetters L, Chen YP, Jonsdottir J, Tronick with cerebral palsy. Adv Physiother 2008;
1: 3–9. EZ. Kicking coordination captures differ- 1: 1–6.
4. Engsberg JR, Ross SA, Collins DR, Park ences between full-term and premature 21. Brunnstrom S. Motor testing procedures
TS. Predicting functional change from infants with white matter disorder. Hum in hemiplegia: based on sequential recov-
preintervention measures in selective dor- Mov Sci 2004; 22: 729–48. ery stages. Phys Ther 1966; 46: 357–75.
sal rhizotomy. J Neurosurg 2007; 106: 14. Berger W, Quintern J, Dietz V. Patho- 22. Fugl-Meyer AR, Jaasko L, Leyman I, Ols-
282–87. physiology of gait in children with cerebral son S, Steglind S. The post-stroke hemi-
5. Sanger TD, Chen D, Delgado MR, Gae- palsy. Electroencephalogr Clin Neurophysiol plegic patient. 1. A method for evaluation
bler-Spira D, Hallett M, Mink JW. Defi- 1982; 53: 538–48. of physical performance. Scand J Rehabil
nition and classification of negative motor 15. Davids JR, Holland WC, Sutherland DH. Med 1975; 7: 13–31.
signs in childhood. Pediatrics 2006; 118: Significance of the confusion test in cere- 23. Olree KS, Engsberg JR, Ross SA, Park
2159–67. bral palsy. J Pediatr Orthop 1993; 13: 717– TS. Changes in synergistic movement pat-
6. Evarts EV. Relation of pyramidal tract 21. terns after selective dorsal rhizotomy. Dev
activity to force exerted during voluntary 16. Rose J, Martin JG, Torburn L, Rinsky LA, Med Child Neurol 2000; 42: 297–303.
movement. J Neurophysiol 1968; 31: 14– Gamble JG. Electromyographic differenti- 24. Thelen DD, Riewald SA, Asakawa DS,
27. ation of diplegic cerebral palsy from idio- Sanger TD, Delp SL. Abnormal coupling
7. Shumway-Cook A, Woollacott MH. pathic toe walking: involuntary of knee and hip moments during maximal
Motor control, theory and practical appli- coactivation of the quadriceps and gastroc- exertions in persons with cerebral palsy.
cations. 2nd edn. Philadelphia: Lippincott nemius. J Pediatr Orthop 1999; 19: 677– Muscle Nerve 2003; 27: 486–93.
Williams and Wilkins, 2001. 82. 25. Domholdt E. Physical therapy research,
8. Staudt M, Pavlova M, Bohm S, Grodd W, 17. Boyd RN, Graham HK. Objective mea- principles and applications. Philadelphia:
Krageloh-Mann I. Pyramidal tract damage surement of clinical findings in the use of WB Saunders, 1993.
correlates with motor dysfunction in bilat- botulinum toxin type A for the manage- 26. Sim J, Arnell P. Measurement validity in
eral periventricular leukomalacia (PVL). ment of children with cerebral palsy. Eur J physical therapy research. Phys Ther 1993;
Neuropediatrics 2003; 34: 182–88. Neurol 1999; 6: S23–35. 73: 102–10.
9. Bax M, Tydeman C, Flodmark O. Clinical 18. Fowler EG, Knutson LM, DeMuth SK, 27. Palisano R, Rosenbaum P, Walter S, Rus-
and MRI correlates of cerebral palsy: the et al. Pediatric endurance and limb strength- sell D, Wood E, Galuppi B. Development
Book Review: Clinical Manual of Child and chapters helpfully cover combination treatments with cog-
Adolescent Psychopharmacology nitive behaviour therapy, as well as paediatric-specific
Edited by Robert L Findling research on suicidality. All of which will prove reassuring
American Psychiatric Publishing, Inc., 2008 to prescribers and patients alike.
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A chapter on bipolar disorders provides a very practical
ISBN 978-1-58562-250-4
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The experts cover developmental aspects vital in under- settings commends this book to a wider medical reader-
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interventions as adjuncts would have been welcome given
more space. Disruptive behaviour disorders and aggression Richard Soppitt MBCHB MRCPSYCH MMEDSC
are considered in a holistic manner whilst reminding clini- Honorary Senior Research Fellow, CHSS, Canterbury, UK.
1 UCLA ⁄ Orthopaedic Hospital Center for Cerebral Palsy, and Tarjan Center for Disabilities at UCLA, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
2 UCLA ⁄ Orthopaedic Hospital Center for Cerebral Palsy, and Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
3 UCLA ⁄ Orthopaedic Hospital Center for Cerebral Palsy, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Correspondence to Dr Eileen G Fowler at University of California, Los Angeles ⁄ Orthopaedic Hospital Center for Cerebral Palsy, 22-64 Rehabilitation Center, 1000 Veteran Avenue, Los Angeles, CA
90095-1795, USA. E-mail: efowler@mednet.ucla.edu
PUBLICATION DATA AIM Multiple impairments contribute to motor deficits in spastic cerebral palsy (CP). Selective
Accepted for publication 15th October 2009. voluntary motor control (SVMC), namely isolation of joint movement upon request, is important,
Published online 18th January 2010. but frequently overlooked. This study evaluated the proximal to distal distribution of SVMC
impairment among lower extremity joints.
LIST OF ABBREVIATIONS METHOD Using a recently developed tool, the Selective Control Assessment of the Lower
CST Corticospinal tract Extremity (SCALE), we evaluated the SVMC of the hip, knee, ankle, subtalar joint, and toes in a
PDC Proximal to distal concordance cross-sectional, observational study of 47 participants with spastic, diplegic, hemiplegic, and
SCALE Selective Control Assessment of the quadriplegic CP (22 males, 25 females; mean age 11y 9mo, SD 4y 8mo; Gross Motor Function
Lower Extremity Classification System levels I–IV).
SVMC Selective voluntary motor control
RESULTS Statistically significant decreases in SCALE scores from hip to toes were found using the
Page statistical test for trend (p<0.001). Statistically significant differences (p<0.05) were found
between all joint pairs, except toes versus subtalar, toes versus ankle, and right ankle versus sub-
talar joints. Cross-tabulation of score frequencies for all pairs revealed that proximal joint scores
were higher or equal to distal ones 81 to 100% of the time. Excluding toes versus subtalar joints,
proximal scores exceeded distal ones 94 to 100% of the time.
INTERPRETATION We confirmed increasing proximal to distal SVMC impairment, which may have
implications for treatment and research.
Individuals with cerebral palsy (CP) have limitations in motor frequent abnormal magnetic resonance imaging (MRI) finding
function resulting from multiple impairments including spas- associated with the spastic diplegic form of CP and it is found
ticity, contractures, weakness, and diminished selective motor in more than one-third of those with hemiplegia and quadri-
control. Selective motor control has been defined as ‘… the plegia.6 Strong correlations between damage to the CSTs and
ability to isolate the activation of muscles in a selected pattern motor impairment have been reported for children with CP.5,7
in response to demands of a voluntary movement or posture.’1 The CSTs have a specific anatomical arrangement as they
Selective voluntary motor control (SVMC) describes the per- descend from the motor cortex to the spinal motor neuron
formance of specific isolated joint movements upon request, as pools.8–10 In the periventricular area, motor fibers leading to
opposed to the habitual activation of selected muscles during the lower extremities are more likely to be damaged than those
functional tasks.2 SVMC at the ankle is a strong predictor of supplying the upper extremities because of their more medial
functional movement ability in children with CP,3 and SVMC position.10 This anatomical relationship has been confirmed
has been used as a prognostic factor in selecting candidates for in recent studies using MRI tractography.11,12 The somato-
selective posterior rhizotomy.4 We recently reported the topic organization of the lower extremity in the sensorimotor
development, validity, and reliability of the Selective Control cortex suggests that distal lower-extremity tracts are closer to
Assessment of the Lower Extremity (SCALE).2 SCALE is a the ventricle and more vulnerable than those of proximal
clinical tool designed to assess SVMC of the entire lower lower-extremity muscles (Fig. 1). Evidence exists of increased
extremity by summing the scores for five joints (hip, knee, distal impairment of lower-extremity motor function in chil-
ankle, subtalar joint, and toes). dren with spastic CP,13–15 but studies specifically examining
Voluntary isolated joint movements require activation of the relationship between SVMC of proximal compared with
the corticospinal tracts (CSTs). In patients with CP, damage distal lower-extremity joints have not been reported. Tedroff
to these tracts commonly occurs in the periventricular area.5 et al.13 evaluated the temporal sequence of muscle recruitment
Damage to the periventricular white matter is the most during maximal voluntary contractions in patients with
264 DOI: 10.1111/j.1469-8749.2009.03586.x ª The Authors. Journal compilation ª Mac Keith Press 2010
Ankle Knee
Table I: Participant characteristics (n=47)
Hip
Age (y:mo)
Arm Mean (SD) 11:9 (4:8)
Range 5:1–23:0
Characteristic (n)
Face Sex
Male 22
Female 25
Distribution of impairment
Diplegia (three had hemiplegic overlay) 35
Hemiplegia 6
Quadriplegia 6
GMFCS-ER level
I 10
II 10
III 18
IV 9
Selective Voluntary Motor Control in Patients with CP Eileen G Fowler et al. 265
2.0
1.8
Figure 2: Mean Selective Control Assessment of the Lower Extremity (SCALE) scores by joint for left and right lower extremities. A score of 0.0 indicates the
participant was unable to isolate or used the full synergy pattern, 1.0 indicates impaired motor control, and 2.0 indicates normal isolated movement. Error bars
represent one standard deviation (+ for left and ) for right). a, significant differences for all joint pairs on both left and right (p<0.05); b, left ankle score was
significantly different from left hip, knee, and subtalar joint scores (p<0.05); c, right ankle joint score was significantly different from right hip and knee
(p<0.05) and showed a tendency toward a difference from the subtalar joint score (p=0.065). Specific p values for all joint pairs are given in Table II.
STJ, subtalar joint.
STJ Toes
0 1 2 0 1 2
0 22 1 0 20 3
Ankle 1 7 9 1 Ankle 1 3 14
PDC 96% 2 4 3 PDC 94% 2 5 2
Toes
0 1 2
0 20 9
STJ 1 3 11
PDC 81% 2 2 2
STJ Toes
0 1 2 0 1 2
0 21 0 19 2
Ankle 1 8 13 2 Ankle 1 5 18
PDC 96% 2 1 2 PDC 96% 2 2 1
Toes
0 1 2
0 22 7
STJ 1 2 12
PDC 85% 2 3 1
Figure 3: Cross-tabulations of Selective Control Assessment of the Lower Extremity score frequencies for (a) left and (b) right lower-extremity joints showing
the percentage proximal to distal concordance (PDC). Shaded zones indicate relationships that violated PDC because the distal joint scores exceeded the
proximal joint scores. STJ, subtalar joint.
deficits when the knee was extended rather than flexed, dem- activated a muscle other than the intended prime mover
onstrating the influence of impaired SVMC. Although these first, especially when the prime mover was a more distal
investigators concluded that distal muscles were generally muscle. These results are consistent with our findings of
weaker than proximal muscles, the hip extensors were an decreased ability to perform isolated joint motion distally.
exception, being weaker than the ankle muscles. As the As Tedroff et al. did not specify whether the participants
SCALE hip test was performed in an antigravity side-lying performed isolated joint motion out of synergy, and we
position, minimizing the need for muscle force-generating did not record electromyograms, direct comparisons are
capacity, we found that SVMC at the hip exceeded that found limited.
at the ankle. Excluding comparisons involving the toes, PDC exceptions
Tedroff et al.13 reported that during maximal voluntary in our study were rare, and could have been caused by scor-
contractions, children with spastic CP more frequently ing errors or other factors affecting patient performance, such
Selective Voluntary Motor Control in Patients with CP Eileen G Fowler et al. 267
as impaired motor planning. Some exceptions to the PDC movement in adults after stroke and is an indicator of the
appeared to be related to the presence of either restricted highest level of recovery for the lower extremity.23 Another
range of motion or mirror movements. Contractures or possible explanation is that moving only one of multiple
severe spasticity can mask underlying SVMC. One 15-year- toe joints was sufficient to obtain a SCALE score of 1,
old participant with spastic diplegia (GMFCS level I) had a reducing the relative potential for a score of 0 at the toes
subtalar score of 2, whereas the more proximal ankle joint compared with the subtalar joint. Finally, there may be
was scored 1, owing to restricted range of motion. As this greater capacity for sparing of corticospinal fibers associ-
study supports increased proximal SVMC, it is possible that ated with toe movement owing to greater density of CSTs.
this participant’s ankle would have been scored 2 if tested at In early mapping studies of the human motor cortex, the
a younger age, before contracture development. The higher area of cortical representation for the great toe was
score at the subtalar joint predicts greater functional exceeded only by the tongue, mouth, thumb, and fingers.8,9
improvement after contracture release than if the score were More recent studies indicate that both toe musculature
1 or 0. This is one example of how SVMC assessment, par- and tibialis anterior have a higher density of associated
ticularly as part of a periodic evaluation for children with monosynaptic corticospinal projections than proximal
spastic CP during development, may be helpful in predicting lower-limb musculature.24
the potential for functional improvement after a specific SVMC assessment and the proximal to distal distribution of
treatment. impairment can be useful in treatment planning and in consid-
Mirror movements are simultaneous, obligatory move- ering prognoses for the development of motor function in
ments that occur at contralateral joints during active young children with CP. Based on the proximal to distal
movement. In adults without disability, most CSTs are increase in SVMC impairment, patients who are assigned a
crossed; however, extensive ipsilateral tracts are normally score of 2 at the ankle or subtalar joint are more likely to have
present in early development. In hemiparetic CP, there is scores of 2 at the knee and hip. Although examining SVMC at
evidence that surviving contralateral tracts may be compet- the individual joint level can be helpful in treatment planning,
itively displaced by persistent ipsilateral tracts20,21, which the SCALE total limb score is more useful when describing a
may be responsible for mirroring.22 Using the SCALE patient’s overall functional ability. For example, we have
tool, a score of 1 is given at a joint when the same move- shown that SCALE total limb scores are significantly related
ment pattern is observed contralaterally. Mirror move- to the performance of simultaneous hip flexion and knee
ments negatively affected the PDC in the less involved extension, as normally occurs, during the terminal swing phase
limb for some participants with asymmetrical CP. In par- of gait.25
ticular, two participants with spastic hemiplegia could iso- We believe this is the first systematic evaluation and
late movement of their ankle joint on their non- comparison of SVMC among multiple lower-extremity
hemiplegic side, but received scores of 1 owing to mirror joints in individuals with spastic CP. It confirms the
ankle movement on their hemiplegic side. Mirroring did increase in severity of impairment from proximal to distal
not occur during subtalar joint testing on their non-hemi- joints. Although previous research supports greater impair-
plegic sides, giving these limbs a score of 2 at the more ment in distal muscles and joints, this phenomenon has
distal joint. Although the presence of mirroring is more received little attention. Anatomical and physiological
likely to reflect a primary pathology for the hemiplegic mechanisms contributing to these findings require further
limb, we assigned the SVMC impairment for the limb study. Our results support selective vulnerability of the
being assessed, as it is movement of this limb that elicits corticospinal tracts innervating distal musculature owing to
the abnormal movement pattern and any resulting func- their proximity to the ventricles. Although the participants
tional problems. The effects of obligatory mirror move- in this study had a clinical diagnosis of spastic CP, damage
ments on functional lower-extremity motor tasks such as to the periventricular white matter was not documented in
walking are unknown and require further study. this sample. Newer technologies allow documentation of
The most frequent exceptions to the PDC occurred precise damage to white matter tracts using MRI with dif-
when the toes were graded as 1 and the subtalar joint was fusion tensor imaging. This may be useful in elucidating
graded as 0, indicating absent subtalar SVMC with sparing the relation between the injury and functional impairment;
at the toes. There are several possible explanations for these studies are currently in progress.
these findings. One may be that the toes are not truly
distal anatomically. Although the insertions of the toe mus- SUPPORTING INFORMATION
culature are more distal, the origin of muscles controlling Additional supporting information is available for this article online:
the ankle, subtalar joint, and toes are similar. In addition, Data S1: The Selective Control Assessment of the Lower Extremity
control of the subtalar joint appears to be more challenging (SCALE), Score Sheet, Directions for Administration and Instructions for
than that of other joints. We observed that isolated motion Grading.
Please note: Wiley-Blackwell are not responsible for the content or func-
of the subtalar joint was the most difficult movement
tionality of any supporting materials supplied by the authors. Any queries
sequence for participants with CP to understand and per-
(other than missing material) should be directed to the corresponding
form. Similar observations have been reported for patients author of the article).
after stroke. Eversion was described as a challenging
Selective Voluntary Motor Control in Patients with CP Eileen G Fowler et al. 269