Evidence map›Paper›PMID 25597614›Full record

ArticleMuscle & nerve2015

Resistance strength training exercise in children with spinal muscular atrophy.

Aga Lewelt, Kristin J Krosschell, Gregory J Stoddard, Cindy Weng, Mei Xue, Robin L Marcus, Eduard Gappmaier, Louis Viollet, Barbara A Johnson, Andrea T White and 5 more

Abstract read
In one paragraph

Article in Muscle & nerve, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Physical exercise training for type 3 spinal muscular atrophy.The Cochrane database of systematic reviews · 2019
    Pooled it
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  12. Creatine monohydrate supplementation for older adults and clinical populations.Journal of the International Society of Sports Nutrition · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Aga LeweltDivision of Physical Medicine and Rehabilitation, Pediatric Motor Disorders Research Program, University of Utah School of Medicine, 30 North 1900 East, Salt Lake City, Utah, 84132, USA.
Kristin J KrosschellDepartment of Physical Therapy and Human Movement Sciences, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Gregory J StoddardStudy Design and Biostatistics Center, University of Utah, Salt Lake City, Utah, USA.
Cindy WengStudy Design and Biostatistics Center, University of Utah, Salt Lake City, Utah, USA.
Mei XueDepartment of Biomedical Informatics, University of Utah, Salt Lake City, Utah, USA.
Robin L MarcusDepartment of Physical Therapy, University of Utah, Salt Lake City, Utah, USA.
Eduard GappmaierDepartment of Physical Therapy, University of Utah, Salt Lake City, Utah, USA.
Louis ViolletDepartment of Neurology, Pediatric Motor Disorders Research Program, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Barbara A JohnsonDepartment of Neurology, Pediatric Motor Disorders Research Program, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Andrea T WhiteDepartment of Exercise and Sport Science, University of Utah, College of Health, Salt Lake City, Utah, USA.
Donata Viazzo-TrussellDepartment of Neurology, Pediatric Motor Disorders Research Program, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Philippe LopesNeuromuscular Degeneration and Plasticity Laboratory, Institut National de la Santé et de la Recherche Médicale UMR-S 1124, University Paris Descartes, Paris, France.
Robert H LaneDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
John C CareyDivision of Pediatric Genetics, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Kathryn J SwobodaDepartment of Neurology, Pediatric Motor Disorders Research Program, University of Utah School of Medicine, Salt Lake City, Utah, USA.
University of Utah · USInserm · FRMedical College of Wisconsin · USNorthwestern University · US

Funding

University of Utah Center for Clinical and Translational ScienceUL1TR001067 · NCATS · UNIVERSITY OF UTAH · PI DERE, WILLARD H., HESS, RACHEL · 2013 to 2017
$19.8M
UNIVERSITY OF UTAH CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE-UL1: BPCAUL1RR025764 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$19.4M
University of Utah Center for Clinical and Translational Science-UL1UL1TR000105 · NCATS · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2012 to 2013
$5.1M
Newborn screening for identification & prospective followup of infants with SMAR01HD069045 · NICHD · UNIVERSITY OF UTAH · PI SWOBODA, KATHRYN J. · 2011 to 2015
$4.3M
Therapeutic Opportunities in Spinal Muscular AtrophyR01HD054599 · NICHD · UNIVERSITY OF UTAH · PI SWOBODA, KATHRYN J. · 2007 to 2011
$1.5M
University of Utah Center for Clinical and Translational Science-KL2KL2RR025763 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$972k
University of Utah Center for Clinical and Translational Science-KL2KL2TR000104 · NCATS · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2012 to 2013
$357k
NCATS NIH HHS 8KL2TR000104NCATS NIH HHS 8UL1TR000105NCATS NIH HHS UL1 TR000105NCATS NIH HHS UL1 TR001067NCRR NIH HHS KL2 RR025763NCRR NIH HHS KL2RR025763NCRR NIH HHS UL1RR025763NCRR NIH HHS UL1 RR025764NCRR NIH HHS UL1RR025764NICHD NIH HHS R01 HD054599NICHD NIH HHS R01-HD054599NICHD NIH HHS R01 HD069045
6 · The paper itself

Abstract

introductionPreliminary evidence in adults with spinal muscular atrophy (SMA) and in SMA animal models suggests exercise has potential benefits in improving or stabilizing muscle strength and motor function.

methodsWe evaluated feasibility, safety, and effects on strength and motor function of a home-based, supervised progressive resistance strength training exercise program in children with SMA types II and III. Up to 14 bilateral proximal muscles were exercised 3 times weekly for 12 weeks.

resultsNine children with SMA, aged 10.4 ± 3.8 years, completed the resistance training exercise program. Ninety percent of visits occurred per protocol. Training sessions were pain-free (99.8%), and no study-related adverse events occurred. Trends in improved strength and motor function were observed.

conclusionsA 12-week supervised, home-based, 3-day/week progressive resistance training exercise program is feasible, safe, and well tolerated in children with SMA. These findings can inform future studies of exercise in SMA.

Indexed as

Treatment OutcomeAdolescentChildChild, PreschoolFemaleHumansMaleMotor ActivityMuscle, SkeletalMuscle StrengthMuscular Atrophy, SpinalReflexReproducibility of ResultsResistance Traininghome-based exercise programneuromuscular disorderprogressive resistance training exercisespinal muscular atrophystrength training exercise

Identifiers

PMID25597614
PMCPMC4506899
OpenAlexW1873534632

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.