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dc.contributor.author
Simon-Martinez, Cristina
dc.contributor.author
Mailleux, Lisa
dc.contributor.author
Ortibus, Els
dc.contributor.author
Fehrenbach, Anna
dc.contributor.author
Sgandurra, Giuseppina
dc.contributor.author
Cioni, Giovanni
dc.contributor.author
Desloovere, Kaat
dc.contributor.author
Wenderoth, Nicole
dc.contributor.author
Demaerel, Philippe
dc.contributor.author
Sunaert, Stefan
dc.contributor.author
Molenaers, Guy
dc.contributor.author
Feys, Hilde
dc.contributor.author
Klingels, Katrijn
dc.date.accessioned
2018-08-07T12:51:44Z
dc.date.available
2018-08-06T18:22:57Z
dc.date.available
2018-08-07T12:51:44Z
dc.date.issued
2018
dc.identifier.issn
1471-2431
dc.identifier.other
10.1186/s12887-018-1228-2
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/280878
dc.identifier.doi
10.3929/ethz-b-000280878
dc.description.abstract
Background Upper limb (UL) deficits in children with unilateral cerebral palsy (uCP) have traditionally been targeted with motor execution treatment models, such as modified Constraint-Induced Movement Therapy (mCIMT). However, new approaches based on a neurophysiological model such as Action-Observation Training (AOT) may provide new opportunities for enhanced motor learning. The aim of this study is to describe a randomised controlled trial (RCT) protocol investigating the effects of an intensive treatment model, combining mCIMT and AOT compared to mCIMT alone on UL function in children with uCP. Additionally, the role of neurological factors as potential biomarkers of treatment response will be analysed. Methods An evaluator-blinded RCT will be conducted in 42 children aged between 6 and 12 years. Before randomization, children will be stratified according to their House Functional Classification Scale, age and type of corticospinal tract wiring. A 2-week day-camp will be set up in which children receive intensive mCIMT therapy for 6 hours a day on 9 out of 11 consecutive days (54 h) including AOT or control condition (15 h). During AOT, these children watch video sequences showing goal-directed actions and subsequently execute the observed actions with the more impaired UL. The control group performs the same actions after watching computer games without human motion. The primary outcome measure will be the Assisting Hand Assessment. Secondary outcomes comprise clinical assessments across body function, activity and participation level of the International Classification of Function, Disability and Health. Furthermore, to quantitatively evaluate UL movement patterns, a three-dimensional motion analysis will be conducted. UL function will be assessed at baseline, immediately before and after intervention and at 6 months follow up. Brain imaging comprising structural and functional connectivity measures as well as Transcranial Magnetic Stimulation (TMS) to evaluate corticospinal tract wiring will be acquired before the intervention. Discussion This paper describes the methodology of an RCT with two main objectives: (1) to evaluate the added value of AOT to mCIMT on UL outcome in children with uCP and (2) to investigate the role of neurological factors as potential biomarkers of treatment response.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
BioMed Central
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Unilateral cerebral palsy
en_US
dc.subject
Upper extremity
en_US
dc.subject
Neuroimaging
en_US
dc.subject
Intensive therapy
en_US
dc.subject
Brain injuries
en_US
dc.subject
Treatment outcome
en_US
dc.title
Combining constraint-induced movement therapy and action-observation training in children with unilateral cerebral palsy: A randomized controlled trial
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
dc.date.published
2018-07-31
ethz.journal.title
BMC Pediatrics
ethz.journal.volume
18
en_US
ethz.journal.issue
1
en_US
ethz.journal.abbreviated
BMC Pediatr
ethz.pages.start
250
en_US
ethz.size
13 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
London
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02070 - Dep. Gesundheitswiss. und Technologie / Dep. of Health Sciences and Technology::02535 - Institut für Bewegungswiss. und Sport / Institut of Human Movement Sc. and Sport::03963 - Wenderoth, Nicole / Wenderoth, Nicole
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02070 - Dep. Gesundheitswiss. und Technologie / Dep. of Health Sciences and Technology::02535 - Institut für Bewegungswiss. und Sport / Institut of Human Movement Sc. and Sport::03963 - Wenderoth, Nicole / Wenderoth, Nicole
ethz.date.deposited
2018-08-06T18:23:15Z
ethz.source
SCOPUS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2018-08-07T12:51:52Z
ethz.rosetta.lastUpdated
2022-03-28T20:50:14Z
ethz.rosetta.versionExported
true
ethz.COinS
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