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dc.date.accessioned2021-03-15T19:36:20Z
dc.date.available2021-03-15T19:36:20Z
dc.date.created2020-05-23T18:42:14Z
dc.date.issued2020
dc.identifier.citationMengshoel, Anne Marit Helland, Ingrid B Meeus, Mira Castro-Marrero, Jesus Pheby, Derek Strand, Elin Bolle . Patients’ experiences and effects of non-pharmacological treatment for myalgic encephalomyelitis/chronic fatigue syndrome – a scoping mixed methods review. International Journal of Qualitative Studies on Health and Well-being. 2020, 15(1)
dc.identifier.urihttp://hdl.handle.net/10852/84077
dc.description.abstractPurpose The EU COST Action 15111 collaboration on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) aims to assess current research and identify knowledge gaps in Europe. Presently, our purpose is to map the effects of non-pharmacological therapies (NPTs) for ME/CFS, and what patients find important in the treatment process. Methods A scoping mixed methods literature review of European studies identified 16 papers fulfiling our inclusion criteria. The quantitative and qualitative studies were synthesized separately in tables. Additionally, extracts from the qualitative studies were subjected to translational analysis. Results Effect studies addressed cognitive behavioural therapy (CBT, n = 4), multimodal rehabilitation (n = 2) and activity-pacing (n = 2). CBT reduced fatigue scores more than usual care or waiting list controls. The effects of rehabilitation and activity-pacing were inconsistent. The contents, assessment methods and effects of rehabilitation and activity pacing studies varied. For patients, health professionals’ recognition of ME/CFS and support were crucial, but they expressed ambiguous experiences of what the NPTs entail. Conclusions Methodological differences make comparisons across NPTs impossible, and from a patient perspective the relevance of the specific contents of NPTs are unclear. Future well-designed studies should focus on developing NPTs tailored to patients’ concerns and evaluation tools reflecting what is essential for patients.
dc.languageEN
dc.publisherCo-Action Publishing
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titlePatients’ experiences and effects of non-pharmacological treatment for myalgic encephalomyelitis/chronic fatigue syndrome – a scoping mixed methods review
dc.typeJournal article
dc.creator.authorMengshoel, Anne Marit
dc.creator.authorHelland, Ingrid B
dc.creator.authorMeeus, Mira
dc.creator.authorCastro-Marrero, Jesus
dc.creator.authorPheby, Derek
dc.creator.authorStrand, Elin Bolle
cristin.unitcode185,52,10,0
cristin.unitnameAvdeling for tverrfaglig helsevitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1812250
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International Journal of Qualitative Studies on Health and Well-being&rft.volume=15&rft.spage=&rft.date=2020
dc.identifier.jtitleInternational Journal of Qualitative Studies on Health and Well-being
dc.identifier.volume15
dc.identifier.issue1
dc.identifier.doihttps://doi.org/10.1080/17482631.2020.1764830
dc.identifier.urnURN:NBN:no-86790
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1748-2623
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/84077/1/Mengshoel%2Bet%2Bal_%2BPatients%2527%2Bexperiences%2Band%2Beffects%2Bof%2Bnon-pharmacological%2Btreatment%2Bfor%2BME_Chronic%2Bfatigue%2Bsyndrome%2B-%2BScoping%2Breview%2B2020.pdf
dc.type.versionPublishedVersion
cristin.articleid1764830
dc.relation.projectCOST/EU kode


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