Evidence map›Paper›PMID 40386421›Full record

ArticleResearch square2025

Effect of EMG-activated vibrotactile biofeedback on skill learning in children with genetic and acquired dystonia during practice of a point-to-point and a cyclic task.

Maral Kasiri, Emilia Ambrosini, Emilia Biffi, Shinichi Amano, Alessandra Pedrocchi, Nardo Nardocci, Elena Beretta, Giovanna Zorzi, Terence D Sanger

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In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Maral KasiriUniversity of California, Irvine.
Emilia AmbrosiniPolitecnico di Milano.
Emilia BiffiScientific Institute for Research, Hospitalization and Healthcare (IRCCS) Eugenio Medea.
Shinichi AmanoUniversity of Southern California.
Alessandra PedrocchiPolitecnico di Milano.
Nardo NardocciIstituto Neurologico Carlo Besta.
Elena BerettaScientific Institute for Research, Hospitalization and Healthcare (IRCCS) Eugenio Medea.
Giovanna ZorziIstituto Neurologico Carlo Besta.
Terence D SangerUniversity of California, Irvine.

Funding

Multi-center trial of Augmented Sensory Feedback in Children with Dyskinetic CPR01HD081346 · NICHD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SANGER, TERENCE D · 2015 to 2019
$2.5M
NICHD NIH HHS R01 HD081346
6 · The paper itself

Abstract

Objective: Dystonia is a movement disorder causing involuntary muscle contractions and abnormal movements. Often, repeated practice does not lead to motor improvement in children with acquired dystonia, likely due to sensory deficits, which may contribute to their impairment. Therefore, improvement of sensory function might improve motor performance. In this study, we propose that an augmented vibrotactile biofeedback may improve motor learning in children with acquired dystonia, but not in children with genetic dystonia, who do not have associated sensory deficits. Design and participants: To test this hypothesis, we recorded muscle activity and kinematic recordings and computed outcome measures that represent motor skills, during practice of a point-to-point movement and trajectory-following task. We examined the effects of applying vibrotactile biofeedback on dystonic muscles, in healthy children and those with genetic and acquired dystonia. Results: The device significantly improved motor learning in children with acquired dystonia, in the cyclic task only, as evidenced by reduced error and improved task correlation index ( Conclusion: Our results show that the vibrotactile device can become an effective method of motor improvement only for cyclic and smooth tasks but not for point-to-point tasks in children with acquired dystonia.

Indexed as

DystoniaMotor ControlRehabilitationSensory DeficitVibrotactile Biofeedback

Identifiers

PMID40386421
PMCPMC12083690

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.