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dc.contributor.authorHammer, Stian
dc.contributor.authorToussaint, Michel
dc.contributor.authorVollsæter, Maria
dc.contributor.authorTvedt, Marianne Nesbjørg
dc.contributor.authorRøksund, Ola Drange
dc.contributor.authorReychler, Gregory
dc.contributor.authorLund, Hans
dc.contributor.authorAndersen, Tiina Maarit
dc.date.accessioned2022-09-01T11:21:45Z
dc.date.available2022-09-01T11:21:45Z
dc.date.created2022-04-30T14:42:37Z
dc.date.issued2022
dc.identifier.citationHammer, S., Toussaint, M., Vollsæter, M., Tvedt, M. N., Røksund, O. D., Reychler, G., Lund, H., & Andersen, T. (2021). Exercise training in Duchenne muscular dystrophy: A systematic review and meta-analysis. Journal of Rehabilitation Medicine, 54.en_US
dc.identifier.issn1650-1977
dc.identifier.urihttps://hdl.handle.net/11250/3015113
dc.description.abstractObjective: To evaluate the effects and safety of exercise training, and to determine the most effective exercise intervention for people with Duchenne muscular dystrophy. Exercise training was compared with no training, placebo or alternative exercise training. Primary outcomes were functioning and health-related quality of life. Secondary outcomes were muscular strength, endurance and lung function. Data sources: A systematic literature search was conducted in Medline, EMBASE, CINAHL, Cochrane Central, PEDro and Scopus. Study selection and data extraction: Screening, data extraction, risk of bias and quality assessment were carried out. Risk of bias was assessed using the Cochrane Collaborations risk of bias tools. The certainty of evidence was assessed using Grading of Recommendations Assessment, Development and Evaluation. Data synthesis: Twelve studies with 282 participants were included. A narrative synthesis showed limited or no improvements in functioning compared with controls. Health-related quality of life was assessed in only 1 study. A meta-analysis showed a significant difference in muscular strength and endurance in favour of exercise training compared with no training and placebo. However, the certainty of evidence was very low. Conclusion: Exercise training may be beneficial in Duchenne muscular dystrophy, but the evidence remains uncertain. Further research is needed on exercise training to promote functioning and health-related quality of life in Duchenne muscular dystrophy.en_US
dc.language.isoengen_US
dc.publisherMedical Journals Swedenen_US
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.subjectDuchenne muscular dystrophyen_US
dc.subjectexercise trainingen_US
dc.subjectrespiratory muscle trainingen_US
dc.subjectrehabilitationen_US
dc.subjectphysiotherapyen_US
dc.titleExercise Training in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysisen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume54en_US
dc.source.journalJournal of Rehabilitation Medicineen_US
dc.identifier.doi10.2340/jrm.v53.985
dc.identifier.cristin2020341
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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