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R E S E A R C H R E P O R T

sEMG Analysis During Landing in Children With Autism Spectrum Disorder: A Pilot
Study
Marcelo R. Rosales, BS; Jennifer Romack, PhD; Rosa Angulo-Barroso, PhD
Department of Kinesiology, California State University, Northridge, California.

Purpose: The aim was to explore the timing and duration of muscle activation during a landing task in children with autism
spectrum disorder (ASD), and compare their responses to those of children who are developing typically (TD).
Methods: Six children (ages 3-4.5 years), half with ASD, hung from a vertical bar, landed, and reacted to a light cue that
signaled the child to run to the right or left or to stay in place. Electromyography and kinematics were recorded and
compared between groups.
Results: Children with ASD had more and longer bursts of muscle activation during preimpact. In contrast, children TD
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displayed more and longer burst of muscle activation during impact.


Conclusion: The results suggest that children with ASD have a less developed landing strategy compared with their peers
TD. Further investigation into the neuromuscular components in children with ASD will guide future interventions for this
population. (Pediatr Phys Ther 2018;30:192–194)
Key words: autism, electromyography, landing

INTRODUCTION et al6 report that children with ASD had lower mean amplitude
Autism spectrum disorder (ASD) is a heterogeneous dis- muscle burst in the gastrocnemius during the stance phase, and
ability affecting 1 in every 68 children in the United States.1 in the rectus femoris during the swing phase, of the gait cycle
Children diagnosed with ASD are typically characterized by compared with children TD. However, no differences between
socioemotional2 and motor behavior deficits.3,4 These motor the groups were found for the biceps femoris or tibialis anterior
behavioral problems have made ASD of interest when it comes (the other muscles examined).
to early interventions to help prevent and improve these motor In addition to walking, jumping and landing are also
deficits. Although extensive behavioral data exist depicting common motor skills of children. Focusing on a fundamental
motor difficulties in children with ASD3,4 and motor interven- motor skill, such as landing, is important, given the established
tions are recommended,5 there are still many unanswered ques- relationship between fundamental motor skill and cognition7
tions about the motor control characteristics of ASD. and physical activty.8 The purpose of this pilot study was to
One aspect that has been explored minimally in children explore the timing and duration of muscle activation during a
with ASD is the neuromuscular components of potential motor landing task in children with ASD and compare their responses
deficits. One group of researchers has explored the neuromus- to children TD. This study is an attempt to expand the literature
cular differences in gross motor behaviors between children with and provide guidance for future research.
ASD and children who are developing typically (TD).6 Mohd

METHODS
Participants
0898-5669/110/3003-0192
Pediatric Physical Therapy
Six children, 3 with ASD and 3 TD between the ages of 3 and
Copyright © 2018 Academy of Pediatric Physical Therapy of the American 4.5 years, participated. Parents provided information regarding
Physical Therapy Association ASD diagnosis. These children were part of a larger study con-
Correspondence: Marcelo R. Rosales, BS, Department of Kinesiology, Cal- ducted at California State University, Northridge, exploring the
ifornia State University, Northridge, 18111 Nordhoff St, Northridge, CA development of landing strategies in children TD. Children were
91330 (marcelo.rosales.826@my.csun.edu). recruited from schools in the San Fernando Valley and service
At the time this article was written, Marcelo Rosales was an undergraduate learning programs at the university. Parents provided informed
student at California State University in the Department of Kinesiology.
consent to participate in the study. The Institutional Review
The authors declare no conflicts of interest.
Board at California State University, Northridge, approved the
DOI: 10.1097/PEP.0000000000000514
study.

192 Rosales et al Pediatric Physical Therapy

Copyright © 2018 Academy of Pediatric Physical Therapy of the American Physical Therapy Association.
Unauthorized reproduction of this article is prohibited.
Procedures This aggregated average was conducted since results were sim-
The participants and their caregivers came to the motor ilar regardless of drop condition (ie, left, right, and stay). Lastly,
development laboratory where a questionnaire regarding diag- interrater reliability for the sEMG data was calculated, achieving
nosis of developmental disabilities was completed. 96.2% agreement for muscle bursts and 91.8% agreement for
Participants were asked to change into compression shorts the timing of onset/offset.
and a tank top and to remove shoes. Anthropometrics, including
leg length, and maximal vertical reach (MVR) and maximal ver- RESULTS
tical jump (MVJ) were assessed and recorded.
Participants
A trained laboratory member placed 10 Trigno Delsys
surface electromyography (sEMG) devices and 15 reflective Three children with ASD (4.18 ± 0.25 years; 66.6% male)
markers on participants. sEMG was placed and recorded on and 3 children with TD (3.63 ± 0.73 years; 66.6% male) had
both sides of the body for gastrocnemius (G), tibialis anterior differences between groups for average height (ASD 110.633 ±
(T), rectus femoris (Q), semitendinosus (H), and erector spinae 2.72 cm, TD 99.13 ± 4.94 cm), weight (ASD 19.23 ± 0.93
(E). Reflective markers were placed on the following anatomical kg, TD 14.8 ± 0.85 kg), and reach height (ASD 135.17 ± 2.75
landmarks: center of the forehead, base of the skull, cervical ver- cm, TD 120.27 ± 2.75 cm). There were no group differences
tebrae 7 (C7), and on both sides for the acromion, lateral epi- in average BMI (ASD 15.75 ± 1.43 kg/m2 , TD 15.08 ± 0.71
condyle of the elbow, greater trochanter of the hip, lateral side of kg/m2 ), leg length (ASD 45.97 ± 2.50 cm, TD 41.30 ± 4.48
the knee, lateral malleolus of the ankle, and the fifth metatarsal. cm), bar height used (ASD 157.52 ± 11.39 cm, TD 139.20 ±
Participants were asked to land from a height-adjusted bar. 11.39 cm), or MVJ (ASD 145.07 ± 7.28 cm, TD 126.30 ± 11.48
Height of the bar was calculated according to the following for- cm) between groups.
mula: Bar height = (40% leg length + 40% MVJ + MVR). For
safety reasons, the individual bar height was tested for each child
Differences in sEMG
using few assisted drops before data collection.
After the bar height was tested and deemed safe, the partic- Differences were found in the duration and percentage of
ipants completed 15 drop trials, where they were asked to land sEMG burst. Participants with TD had longer burst during
onto 2 force plates (Kistler, 9286BA; one foot on each force plate) impact for G (left and right), T (left), and H (left and right). The
and react to a randomized light cue. The light cue instructed the children with ASD had longer burst during preimpact for E (left
child to stay in place (stay trial), or to run to the left or right (left and right) and G (right) (Figure). The Figure graphs the average
or right trials). Five trials for each condition were completed per onset/offset times and the average length of muscle bursts during
condition. preimpact (A) and impact for both groups (B). Postimpact data
had fewer differences between the groups for onset/offset time
and durations and therefore were not presented.
Surface Electromyography Children TD, on average, had a greater percentage of trials
that included an EMG burst in E (left [ASD 45.0% ± 21.0%, TD
Delsys EMG Works software was used to rectify and smooth
69.8 ± 27.5%] and right [ASD 50.2% ± 19.9%, TD 69.3% ±
the sEMG data using a root mean square technique (window
17.5%]), G (left [ASD 60.6% ± 19.6%, TD 79.4% ± 14.2%]),
length 0.1 seconds, window overlap 0.005 seconds). For each
and Q (left [ASD 43.4% ± 28.6%, TD 71.3% ± 26.2%]) at
sEMG channel, 2 independent coders manually identified the
postimpact; and H (right [ASD 94.3% ± 8.6%, TD 100% ±
onset/offset of muscle bursts (≥80 ms) during preimpact (750
0%]) and E (right [ASD 94.3% ± 8.4%, TD 100% ± 0%]) at
ms before), impact, and postimpact (750 ms after). The onset
impact. Taken together, these results indicate that children with
and offset times, the duration of the burst, and percentages of
ASD had longer muscle bursts prior to impact, whereas children
trials that contained a muscle burst were calculated.
TD had longer and more muscle activation at and after impact.

Kinematics Kinematics
A Qualisys three-dimensional motion capture system was No differences were found between the groups for the angle
used to collect kinematic data. Hip and knee angles at impact of the knee and hip at impact or maximum flexion. However,
and maximum flexion were calculated. The duration from there were differences in the duration from impact to maximum
impact to maximum hip and knee flexion was calculated. knee (ASD 1.09 ± 0.25 seconds, TD 0.99 ± 0.15 seconds) and
hip flexion (ASD 1.14 ± 0.2 seconds, TD 1.07 ± 0.11 seconds).
Children TD had shorter duration for both maximum knee and
Statistical Analysis hip flexion.
Descriptive statistics were calculated for anthropometric,
sEMG, and kinematic variables using SPSS v.22. Independent
t tests were used to guide our exploration of the data but not DISCUSSION
to determine statistical significance. Results with P values lower The results from this pilot study support that children TD
than .05 are reported. Mean values across all trials for the sEMG had more and longer sEMG bursts during impact compared with
and kinematic data are presented and used to compare groups. children with ASD. Prior literature in children TD suggests that

Pediatric Physical Therapy sEMG Analysis During Landing in Children With ASD 193

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Unauthorized reproduction of this article is prohibited.
vation postimpact, children TD were exhibiting a more effi-
cient landing strategy from impact to maximum flexion and
postimpact. However, further study is needed to investigate this
claim.
There were no significant differences in maximum hip and
knee flexion. Lack of group differences may be explained by a
small sample size (low power) and/or large variability in the
kinematics. However, no angular amplitude differences in the
lower extremity may exist between these 2 populations during
landing. The only differences might be in the timing variables
and duration of muscle activation. If this is accurate, observation
of movement amplitude patterns in young children with ASD
may not elucidate underlying neuromuscular deficiency. Cau-
tion should be used in interpreting our results. Further inves-
tigation is needed using a larger sample size and more robust
kinematics.
Due to the limitations of this pilot study, we can only sug-
gest that differences in sEMG may exist between children with
and without ASD. If correct, our findings might have thera-
peutic relevance, suggesting that interventions for children with
ASD should target muscle activation timing to prevent poten-
tial deficits in landing, a skill widely used for all children during
recreational and structured physical activities.

ACKNOWLEDGMENTS
Thank you to all of the participants and their families for
Fig. sEMG onsets and offsets for all conditions during preimpact (A) and impact being part of the study. Also, a special thank you to the labora-
(B). Length of the vertical bars indicates duration of the muscle burst. Horizontal tory interns in the laboratory that helped with the project.
black continuous line denotes impact. Horizontal black dashed line denotes max
hip flexion for ASD. Horizontal gray dashed line denotes max hip flexion for TD.
The circled muscles indicate group differences. ASD indicates autism spectrum REFERENCES
disorder; E, erector spinae; G, gastrocnemius; H, semitendinosus; L, left; Q, rectus
femoris; R, right; T, tibialis anterior; TD, typical development. 1. Centers for Disease Control and Prevention. Prevalence of autism spec-
trum disorder among children aged 8 years—autism and developmental
disabilities monitoring network, 11 sites, United States, 2010. MMWR
Surveill Summ. 2014;63:1-21.
longer bursts of muscle activation, during what we defined as 2. America Psychiatric Association. Neurodevelopmental disorders. In:
impact, represent a more mature landing strategy.9,10 In con- Diagnostic and Statistical Manual of Mental Disorders: DSM-5. 5th ed.
trast, children with ASD may have longer preactivations com- Washington, DC: American Psychiatric Association Publishing; 2013:
50-59.
pared with children TD for some muscles. These results indi-
3. Whyatt CP, Craig CM. Motor skills in children aged 7-10 years, diag-
cate a less developed landing strategy in children with ASD, nosed with autism spectrum disorder. J Autism Dev Disord. 2012;42(9):
as defined by the timing of muscle activation. Compared with 1799-1809.
previous studies,3,4 our results are in agreement with a devel- 4. Staples KL, Reid G. Fundamental movement skills and autism spectrum
opmental delay in ASD, although our data included a younger disorders. J Autism Dev Disord. 2010;40(2):209-217.
5. Downey R, Rapport MJ. Motor activity in children with autism: a review
cohort.
of current literature. Pediat Phys Ther. 2012;24(1):2-20.
The various landing conditions (stay, left, and right) had 6. Mohd MN, Jailani R, Tahir NM, et al. EMG signals analysis of BF and RF
similar results for both kinematics and sEMG data. This could muscles in autism spectrum disorder (ASD) during walking. Int J Adv
be due to the fact that the light cue was triggered as the landing Sci Eng Inform Technol. 2016;6(5):793-798.
was initiated, and therefore, children may have performed this 7. Lopes L, Santos R, Pereira B, Lopes VP. Associations between gross
motor coordination and academic achievement in elementary school
task as 2 separate actions (land and stay, or land and run). A
children. Hum Mov Sci. 2013;32(1):9-20.
more detailed analysis of the postimpact data including reaction 8. Barnett LM, Van Beurden E, Morgan PJ, Brooks LO, Beard JR. Childhood
time, and stepping and attention strategies, where potential con- motor skill proficiency as a predictor of adolescent physical activity. J
dition differences may exist, might provide insight into group Adolesc Health. 2009;44(3):252-259.
differences in the decision-making process for our task. 9. Christoforidou A, Patikas DA, Bassa E, et al. Landing from dif-
ferent heights: biomechanical and neuromuscular strategies in trained
Kinematic differences were found in the duration from
gymnasts and untrained prepubescent girls. J Electromyogr Kinesiol.
impact to maximum knee and hip flexion. Children TD showed 2017;32:1-8.
shorter duration to achieve maximum knee and hip flexion. 10. Lazaridis S, Bassa E, Patikas D, Giakas G, Gollhofer A, Kotzamanidis C.
Paired with the results from the sEMG data, where most Neuromuscular differences between prepubescents boys and adult men
extensor muscles (E, Q, and G) had greater percentage of acti- during drop jump. Eur J Appl Physiol, 2010;110(1):67-74.

194 Rosales et al Pediatric Physical Therapy

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Unauthorized reproduction of this article is prohibited.

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