Evidence map›Paper›PMID 42112687›Full record

ArticleJournal of pediatric rehabilitation medicine2026

Home-based exercise training in boys with Duchenne muscular dystrophy: A 12-month intervention study.

Stian Hammer, Maria Vollsæter, Michel Toussaint, Ola Drange Røksund, Guri Brekke, Bjørge Herman Hansen, Haakon Krisitian Kvidaland, Lars Peder Bovim, Roy Miodini Nilsen, Tiina Andersen

Abstract read
In one paragraph

Article in Journal of pediatric rehabilitation medicine, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Stian HammerDepartment of Physiotherapy, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0003-2254-7704
Maria VollsæterDepartment of Paediatric and Adolescent Medicine, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0003-2545-0190
Michel ToussaintDepartment of Neurology, Centre de Référence Neuromusculaire, ULB Hôpital Universitaire de Bruxelles (H.U.B.), Brussels, Belgium.ORCID 0000-0002-5939-9955
Ola Drange RøksundDepartment of Health and Functioning, Western Norway University of Applied Sciences, Bergen, Norway.ORCID 0000-0002-8381-0142
Guri BrekkeDepartment of Physiotherapy, Haukeland University Hospital, Bergen, Norway.
Bjørge Herman HansenDepartment of Sport Sciences and Physical Education, University of Agder, Kristiansand, Norway.ORCID 0000-0001-8445-8227
Haakon Krisitian KvidalandDepartment of Health and Functioning, Western Norway University of Applied Sciences, Bergen, Norway.ORCID 0000-0002-0836-5958
Lars Peder BovimDepartment of Health and Functioning, Western Norway University of Applied Sciences, Bergen, Norway.ORCID 0000-0003-1865-7388
Roy Miodini NilsenDepartment of Health and Functioning, Western Norway University of Applied Sciences, Bergen, Norway.ORCID 0000-0002-6340-4593
Tiina AndersenDepartment of Health and Functioning, Western Norway University of Applied Sciences, Bergen, Norway.ORCID 0000-0002-0641-3653

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PurposeDuchenne muscular dystrophy (DMD) is a progressive X-linked neuromuscular disorder that reduces physical activity (PA) levels and leads to early loss of ambulation. The World Health Organization recommends promoting daily PA for children with disabilities. The primary aim of this study was to assess changes in PA level, physical function, and quality of life (QoL) after one year of a home-based exercise program in boys with DMD. Secondarily, it aimed to evaluate the suitability and safety of the exercise program for this patient group.MethodsIn this prospective longitudinal intervention study, 12 boys with DMD (ambulatory and non-ambulatory) participated in an individually tailored program combining strength and endurance training three times per week for one year. Another 11 boys with DMD served as a non-intervention comparison group. PA-levels were monitored using accelerometery. Secondary outcomes included upper-limb function, lung function, grip strength, endurance, and health-related QoL.ResultsLight and moderate-to-vigorous PA-levels increased in the intervention group but declined in the non-intervention group. Sedentary time increased in both groups. No adverse events were related to the intervention. While upper-limb function declined, other measures remained stable, with a small improvement in QoL.ConclusionHome-based, moderate-intensity exercise appears to be beneficial and safe, and may sustain PA-levels, functional abilities, and QoL in boys with DMD.

Indexed as

Exercise TherapyMuscular Dystrophy, DuchenneAdolescentChildHumansLongitudinal StudiesMaleProspective StudiesQuality of LifeTreatment OutcomeDuchenne muscular dystrophyexercise trainingpaediatric & adolescent rehabilitationphysical activityphysical therapy

Identifiers

PMID42112687
PMCPMC13442673

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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.